Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5733 |
| ensemblid | ENSG00000050628.21 |
| hgncid | 9595 |
| symbol | PTGER3 |
| name | prostaglandin E receptor 3 |
| refseq_nuc | NM_198719.2 |
| refseq_prot | NP_942012.1 |
| ensembl_nuc | ENST00000306666.10 |
| ensembl_prot | ENSP00000302313.5 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 70970782 |
| end | 71047816 |
| strand | - |
| ver | v1.2 |
| region | chr1:70970782-71047816 |
| region5000 | chr1:70965782-71052816 |
| regionname0 | PTGER3_chr1_70970782_71047816 |
| regionname5000 | PTGER3_chr1_70965782_71052816 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 389 | 360 | 81 | 61 | 164 | 14 | 38 | 128 | PTGER3_chr1_70965782_71052816 | PTGER3 | MKETR others(384): Show |
chr1 | 70965782 | 71052816 |
| a0002 | 0/0 | 389 | 7 | 0 | 2 | 5 | 0 | 0 | 5 | PTGER3_chr1_70965782_71052816 | PTGER3 | MKETR others(384): Show |
chr1 | 70965782 | 71052816 |
| a0003 | 0/0 | 389 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | MKETR others(384): Show |
chr1 | 70965782 | 71052816 |
| a0004 | 0/0 | 225 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | MKETR others(220): Show |
chr1 | 70965782 | 71052816 |
| a0005 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | MKETR others(384): Show |
chr1 | 70965782 | 71052816 |
| a0006 | 0/0 | 389 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | MKETR others(384): Show |
chr1 | 70965782 | 71052816 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1169 | 331 | 58 | 56 | 164 | 13 | 38 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0001c0002 | 0/0 | 1169 | 21 | 16 | 4 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0001c0004 | 0/0 | 1169 | 6 | 6 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0001c0007 | 0/0 | 1169 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0001c0009 | 0/0 | 1169 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0002c0003 | 0/0 | 1169 | 7 | 0 | 2 | 5 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0003c0005 | 0/0 | 1169 | 2 | 1 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0004c0010 | 0/0 | 1120 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1115): Show |
chr1 | 70965782 | 71052816 | ||
| a0005c0006 | 0/0 | 1169 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 | ||
| a0006c0008 | 0/0 | 1169 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | ATGAA others(1164): Show |
chr1 | 70965782 | 71052816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2359 | 237 | 34 | 41 | 121 | 10 | 30 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0001t0002 | 0/1 | 2359 | 81 | 20 | 12 | 42 | 1 | 5 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0001t0003 | 0/0 | 2359 | 7 | 0 | 3 | 0 | 1 | 3 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0001t0004 | 0/0 | 2359 | 2 | 2 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0001t0005 | 0/0 | 2359 | 2 | 2 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0001t0008 | 0/0 | 2359 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0001t0009 | 0/0 | 2359 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0002t0001 | 0/0 | 2359 | 19 | 14 | 4 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0002t0006 | 0/0 | 2359 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0002t0010 | 0/0 | 2359 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0004t0002 | 0/0 | 2359 | 6 | 6 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0007t0001 | 0/0 | 2359 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0001c0009t0007 | 0/0 | 2359 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0002c0003t0001 | 0/0 | 2359 | 7 | 0 | 2 | 5 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0003c0005t0002 | 0/0 | 2359 | 2 | 1 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0004c0010t0002 | 0/0 | 2310 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2305): Show |
chr1 | 70965782 | 71052816 |
| a0005c0006t0001 | 0/0 | 2359 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| a0006c0008t0002 | 0/0 | 2359 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | GCCTC others(2354): Show |
chr1 | 70965782 | 71052816 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0312 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0010g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0007t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0009t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0003c0005t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0003c0005t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0004c0010t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0005c0006t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0006c0008t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0324 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0347 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00609 | hp1 | a0001 | c0001 | t0009 | g0067 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00639 | hp2 | a0003 | c0005 | t0002 | g0290 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0267 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0348 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0239 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0328 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0346 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0325 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01884 | hp1 | a0001 | c0009 | t0007 | g0337 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0351 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02004 | hp1 | a0001 | c0007 | t0001 | g0178 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0332 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02145 | hp1 | a0004 | c0010 | t0002 | g0344 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CDX | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0330 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0321 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0333 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0322 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0319 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0350 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0339 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0334 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02922 | hp2 | a0001 | c0002 | t0010 | g0352 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0320 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0342 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0335 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0323 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03209 | hp1 | a0001 | c0004 | t0002 | g0341 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03516 | hp2 | a0005 | c0006 | t0001 | g0017 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0340 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0336 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0349 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18906 | hp1 | a0001 | c0004 | t0002 | g0343 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18946 | hp2 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18956 | hp2 | a0006 | c0008 | t0002 | g0043 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0199 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19043 | hp1 | a0001 | c0002 | t0006 | g0326 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0227 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0242 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ASW | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ASW | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0311 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0141 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0338 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG06807 | hp1 | a0003 | c0005 | t0002 | g0289 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0305 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0312 | REF | REF | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0103 | REF | REF | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70974342 | G | A | 1 | a0003 | 2 | HG00639.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.1124C>T | p.Pro375Leu | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/4 | 1363/2360 | 1124/1173 | 375/390 | chr1 | 70974342 | |||
| chr1:70974369 | T | C | 1 | a0002 | 7 | HG00642.hp2 HG00741.hp2 NA18946.hp2 others(4): Show |
missense_variant | MODERATE | c.1097A>G | p.Asn366Ser | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/4 | 1336/2360 | 1097/1173 | 366/390 | chr1 | 70974369 | |||
| chr1:71012426 | G | A | 1 | a0006 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.956C>T | p.Thr319Met | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/4 | 1195/2360 | 956/1173 | 319/390 | chr1 | 71012426 | |||
| chr1:71046878 | AGGCAGAG others(42): Show |
A | 1 | a0004 | 1 | HG02145.hp1 | frameshift_variant | HIGH | c.651_699delCGGGACTA others(41): Show |
p.Gly218fs | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/4 | 938/2360 | 651/1173 | 217/390 | chr1 | 71046878 | |||
| chr1:71047454 | C | T | 1 | a0005 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.124G>A | p.Gly42Arg | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/4 | 363/2360 | 124/1173 | 42/390 | chr1 | 71047454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:71012425 | C | T | 1 | a0001c0007 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.957G>A | p.Thr319Thr | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/4 | 1196/2360 | 957/1173 | 319/390 | chr1 | 71012425 | |||
| chr1:71046960 | C | A | 1 | a0001c0002 | 21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
synonymous_variant | LOW | c.618G>T | p.Thr206Thr | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/4 | 857/2360 | 618/1173 | 206/390 | chr1 | 71046960 | |||
| chr1:71047257 | G | A | 1 | a0001c0009 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.321C>T | p.Thr107Thr | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/4 | 560/2360 | 321/1173 | 107/390 | chr1 | 71047257 | |||
| chr1:71047467 | G | C | 2 | a0001c0004 a0004c0010 |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
synonymous_variant | LOW | c.111C>G | p.Leu37Leu | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/4 | 350/2360 | 111/1173 | 37/390 | chr1 | 71047467 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70970850 | G | A | 1 | a0001c0001t0009 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*880C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 880 | chr1 | 70970850 | ||||||
| chr1:70970900 | A | G | 1 | a0001c0001t0008 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 830 | chr1 | 70970900 | ||||||
| chr1:70970961 | T | C | 1 | a0001c0001t0004 | 2 | HG02630.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*769A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 769 | chr1 | 70970961 | ||||||
| chr1:70970990 | G | A | 1 | a0001c0001t0005 | 2 | HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*740C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 740 | chr1 | 70970990 | ||||||
| chr1:70971064 | C | A | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0004t0002 others(3): Show |
97 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*666G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 666 | chr1 | 70971064 | ||||||
| chr1:70971209 | A | G | 1 | a0001c0009t0007 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 521 | chr1 | 70971209 | ||||||
| chr1:70971273 | A | G | 1 | a0001c0002t0006 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*457T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 457 | chr1 | 70971273 | ||||||
| chr1:70971668 | G | A | 1 | a0001c0001t0005 | 2 | HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 4/4 | 62 | chr1 | 70971668 | ||||||
| chr1:71047606 | G | A | 1 | a0001c0001t0003 | 7 | HG00280.hp2 HG00741.hp1 HG01168.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/4 | chr1 | 71047606 | |||||||
| chr1:71047746 | G | A | 1 | a0001c0002t0010 | 1 | HG02922.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-169C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/4 | chr1 | 71047746 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:70971788 | T | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0274 a0001c0001t0001g0276 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1170-55A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70971788 | |||||||
| chr1:70972053 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1170-320G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972053 | |||||||
| chr1:70972093 | C | T | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(55): Show |
61 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1170-360G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972093 | |||||||
| chr1:70972094 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1170-361C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972094 | |||||||
| chr1:70972256 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1170-523C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972256 | |||||||
| chr1:70972274 | G | C | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1170-541C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972274 | |||||||
| chr1:70972308 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1170-575G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972308 | |||||||
| chr1:70972358 | G | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1170-625C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972358 | |||||||
| chr1:70972409 | T | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(297): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1170-676A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972409 | |||||||
| chr1:70972417 | C | T | 347 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.1170-684G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972417 | |||||||
| chr1:70972478 | A | G | 1 | a0001c0001t0002g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1170-745T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972478 | |||||||
| chr1:70972529 | A | AAT | 4 | a0001c0001t0002g0078 a0001c0001t0002g0315 a0003c0005t0002g0289 others(1): Show |
4 | HG00639.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170-798_1170-797d others(4): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972529 | |||||||
| chr1:70972604 | T | C | 2 | a0001c0001t0004g0075 a0001c0001t0004g0280 |
2 | HG02630.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1170-871A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972604 | |||||||
| chr1:70972613 | C | A | 1 | a0001c0002t0001g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1170-880G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972613 | |||||||
| chr1:70972753 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0136 a0001c0001t0001g0218 |
3 | HG00140.hp1 HG03490.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1170-1020C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972753 | |||||||
| chr1:70972806 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1170-1073T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972806 | |||||||
| chr1:70972819 | G | T | 1 | a0001c0001t0001g0252 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1170-1086C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972819 | |||||||
| chr1:70972899 | T | C | 2 | a0001c0001t0005g0107 a0001c0001t0005g0275 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1170-1166A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972899 | |||||||
| chr1:70973014 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1170-1281C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973014 | |||||||
| chr1:70973033 | G | GAGATGGA others(4): Show |
187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1169+1253_1169+126 others(15): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973033 | |||||||
| chr1:70973053 | C | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1169+1244G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973053 | |||||||
| chr1:70973121 | C | CGT | 4 | a0001c0001t0001g0145 a0001c0002t0001g0329 a0001c0002t0001g0336 others(1): Show |
4 | HG00639.hp1 HG02922.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+1174_1169+117 others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973121 | |||||||
| chr1:70973121 | C | CGTGT | 3 | a0001c0001t0001g0153 a0001c0002t0001g0328 a0001c0002t0001g0333 |
3 | HG01074.hp1 HG02572.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1169+1172_1169+117 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973121 | |||||||
| chr1:70973121 | C | CGTGTGT | 9 | a0001c0001t0002g0158 a0001c0001t0002g0159 a0001c0001t0002g0288 others(6): Show |
9 | HG01071.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1169+1170_1169+117 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973121 | |||||||
| chr1:70973121 | CGT | C | 257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(254): Show |
269 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.1169+1174_1169+117 others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973121 | |||||||
| chr1:70973121 | CGTGT | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0262 others(7): Show |
10 | HG01255.hp1 HG01346.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1169+1172_1169+117 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973121 | |||||||
| chr1:70973131 | T | G | 2 | a0001c0001t0001g0271 a0001c0009t0007g0337 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1169+1166A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973131 | |||||||
| chr1:70973202 | TGATA | T | 17 | a0001c0001t0001g0025 a0001c0001t0001g0072 a0001c0001t0001g0193 others(14): Show |
17 | HG00621.hp1 HG01069.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1169+1091_1169+109 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973202 | |||||||
| chr1:70973213 | TAGATAGA others(5): Show |
T | 1 | a0001c0001t0001g0233 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1169+1072_1169+108 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973213 | |||||||
| chr1:70973213 | TAGATAGA others(13): Show |
T | 1 | a0001c0002t0010g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1169+1064_1169+108 others(24): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973213 | |||||||
| chr1:70973217 | TA | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0217 a0001c0001t0001g0251 others(2): Show |
5 | HG01934.hp1 HG01978.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169+1079delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973217 | |||||||
| chr1:70973217 | TAGATGAT others(1): Show |
T | 35 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(32): Show |
37 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.1169+1072_1169+107 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973217 | |||||||
| chr1:70973217 | TAGATGAT others(5): Show |
T | 3 | a0001c0001t0001g0268 a0001c0002t0001g0335 a0002c0003t0001g0242 |
3 | HG03098.hp2 NA18944.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1169+1068_1169+107 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973217 | |||||||
| chr1:70973217 | TAGATGAT others(9): Show |
T | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1169+1064_1169+107 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973217 | |||||||
| chr1:70973221 | T | TA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0217 a0001c0001t0001g0251 others(2): Show |
5 | HG01934.hp1 HG01978.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169+1075_1169+107 others(5): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973221 | |||||||
| chr1:70973221 | T | TGATA | 5 | a0001c0001t0001g0218 a0001c0001t0001g0237 a0001c0001t0001g0244 others(2): Show |
5 | HG02280.hp1 HG03225.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169+1072_1169+107 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973221 | |||||||
| chr1:70973221 | TGATA | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0029 others(83): Show |
87 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1169+1072_1169+107 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973221 | |||||||
| chr1:70973221 | TGATAGAT others(1): Show |
T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
104 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1169+1068_1169+107 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973221 | |||||||
| chr1:70973221 | TGATAGAT others(5): Show |
T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0038 others(13): Show |
16 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1169+1064_1169+107 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973221 | |||||||
| chr1:70973221 | TGATAGAT others(9): Show |
T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1169+1060_1169+107 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973221 | |||||||
| chr1:70973229 | A | AGATAGAT others(8): Show |
1 | a0001c0001t0005g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1169+1053_1169+106 others(19): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973229 | |||||||
| chr1:70973233 | A | AGATAGAT others(4): Show |
1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1169+1053_1169+106 others(15): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973233 | |||||||
| chr1:70973672 | C | A | 2 | a0001c0001t0002g0076 a0006c0008t0002g0043 |
2 | NA18956.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1169+625G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973672 | |||||||
| chr1:70973764 | A | G | 1 | a0001c0002t0010g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1169+533T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973764 | |||||||
| chr1:70973845 | C | A | 92 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0026 others(89): Show |
93 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1169+452G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973845 | |||||||
| chr1:70973907 | G | A | 92 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0026 others(89): Show |
93 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1169+390C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973907 | |||||||
| chr1:70973948 | G | A | 7 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0045 others(4): Show |
7 | NA18944.hp2 NA18960.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1169+349C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973948 | |||||||
| chr1:70973975 | G | C | 93 | a0001c0001t0001g0102 a0001c0001t0002g0003 a0001c0001t0002g0023 others(90): Show |
94 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1169+322C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973975 | |||||||
| chr1:70974050 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1169+247A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70974050 | |||||||
| chr1:70974109 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0092 |
4 | HG02132.hp1 NA18979.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+188A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70974109 | |||||||
| chr1:70974194 | T | G | 4 | a0001c0001t0002g0078 a0001c0001t0002g0315 a0003c0005t0002g0289 others(1): Show |
4 | HG00639.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169+103A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70974194 | |||||||
| chr1:70974235 | C | T | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1169+62G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70974235 | |||||||
| chr1:70974480 | T | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0083 others(1): Show |
5 | HG02071.hp1 NA18747.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-92A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70974480 | |||||||
| chr1:70974534 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
198 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1078-146G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70974534 | |||||||
| chr1:70974585 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0087 others(3): Show |
6 | HG01943.hp1 HG02148.hp2 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-197G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70974585 | |||||||
| chr1:70974618 | T | C | 1 | a0001c0002t0001g0016 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1078-230A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70974618 | |||||||
| chr1:70975043 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1078-655C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975043 | |||||||
| chr1:70975364 | CT | C | 98 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0026 others(95): Show |
99 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1078-977delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975364 | |||||||
| chr1:70975410 | C | G | 98 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0026 others(95): Show |
99 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1078-1022G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975410 | |||||||
| chr1:70975447 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-1059C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975447 | |||||||
| chr1:70975596 | C | A | 2 | a0002c0003t0001g0198 a0002c0003t0001g0226 |
2 | NA18946.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1078-1208G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975596 | |||||||
| chr1:70975610 | A | G | 10 | a0001c0001t0001g0106 a0001c0002t0001g0328 a0001c0002t0001g0329 others(7): Show |
10 | HG01074.hp1 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-1222T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975610 | |||||||
| chr1:70975669 | A | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1078-1281T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975669 | |||||||
| chr1:70975765 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1078-1377G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975765 | |||||||
| chr1:70975865 | C | G | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1078-1477G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975865 | |||||||
| chr1:70975912 | G | A | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-1524C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975912 | |||||||
| chr1:70976116 | TA | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(140): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1078-1729delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976116 | |||||||
| chr1:70976269 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-1881C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976269 | |||||||
| chr1:70976383 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1078-1995T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976383 | |||||||
| chr1:70976390 | C | A | 2 | a0001c0001t0001g0314 a0001c0001t0002g0315 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-2002G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976390 | |||||||
| chr1:70976443 | G | A | 62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(59): Show |
65 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.1078-2055C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976443 | |||||||
| chr1:70976513 | T | A | 1 | a0001c0002t0010g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1078-2125A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976513 | |||||||
| chr1:70976523 | C | T | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1078-2135G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976523 | |||||||
| chr1:70976577 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1078-2189A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976577 | |||||||
| chr1:70976654 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1078-2266A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976654 | |||||||
| chr1:70976686 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0228 |
3 | HG01943.hp2 HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1078-2298C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976686 | |||||||
| chr1:70976738 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1078-2350A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976738 | |||||||
| chr1:70976761 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-2373T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976761 | |||||||
| chr1:70976774 | T | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(281): Show |
297 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.1078-2386A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976774 | |||||||
| chr1:70976943 | T | C | 89 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0063 others(86): Show |
90 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1078-2555A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976943 | |||||||
| chr1:70977000 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1078-2612A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977000 | |||||||
| chr1:70977029 | T | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-2641A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977029 | |||||||
| chr1:70977054 | G | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1078-2666C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977054 | |||||||
| chr1:70977056 | T | C | 1 | a0001c0004t0002g0341 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1078-2668A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977056 | |||||||
| chr1:70977061 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1078-2673C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977061 | |||||||
| chr1:70977119 | G | A | 1 | a0001c0001t0002g0305 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1078-2731C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977119 | |||||||
| chr1:70977214 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1078-2826G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977214 | |||||||
| chr1:70977219 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1078-2831G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977219 | |||||||
| chr1:70977288 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(330): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1078-2900A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977288 | |||||||
| chr1:70977383 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1078-2995G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977383 | |||||||
| chr1:70977400 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1078-3012A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977400 | |||||||
| chr1:70977420 | G | T | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1078-3032C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977420 | |||||||
| chr1:70977444 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1078-3056T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977444 | |||||||
| chr1:70977452 | T | G | 89 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0063 others(86): Show |
90 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1078-3064A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977452 | |||||||
| chr1:70977467 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1078-3079A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977467 | |||||||
| chr1:70977522 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1078-3134G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977522 | |||||||
| chr1:70977672 | C | A | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-3284G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977672 | |||||||
| chr1:70977716 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(306): Show |
322 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.1078-3328G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977716 | |||||||
| chr1:70977831 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1078-3443C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977831 | |||||||
| chr1:70977971 | C | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0225 a0001c0001t0001g0264 |
3 | HG02523.hp1 NA18939.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1078-3583G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977971 | |||||||
| chr1:70978309 | A | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-3921T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978309 | |||||||
| chr1:70978397 | A | G | 71 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0063 others(68): Show |
72 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1078-4009T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978397 | |||||||
| chr1:70978406 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1078-4018C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978406 | |||||||
| chr1:70978466 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1078-4078T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978466 | |||||||
| chr1:70978530 | G | A | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-4142C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978530 | |||||||
| chr1:70978546 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-4158C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978546 | |||||||
| chr1:70978672 | T | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1078-4284A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978672 | |||||||
| chr1:70978864 | C | G | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-4476G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978864 | |||||||
| chr1:70978882 | G | T | 10 | a0001c0001t0001g0106 a0001c0002t0001g0328 a0001c0002t0001g0329 others(7): Show |
10 | HG01074.hp1 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-4494C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978882 | |||||||
| chr1:70978951 | T | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-4563A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70978951 | |||||||
| chr1:70979003 | C | A | 1 | a0001c0001t0002g0035 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1078-4615G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979003 | |||||||
| chr1:70979021 | C | A | 7 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(4): Show |
7 | HG01255.hp1 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-4633G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979021 | |||||||
| chr1:70979068 | G | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1078-4680C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979068 | |||||||
| chr1:70979276 | G | C | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG02698.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1078-4888C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979276 | |||||||
| chr1:70979304 | G | GA | 7 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0087 others(4): Show |
7 | HG01943.hp1 HG02148.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-4917dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979304 | |||||||
| chr1:70979405 | A | AAAG | 49 | a0001c0001t0001g0029 a0001c0001t0001g0063 a0001c0001t0001g0102 others(46): Show |
50 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1078-5020_1078-501 others(7): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979405 | |||||||
| chr1:70979427 | T | A | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-5039A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979427 | |||||||
| chr1:70979500 | T | TG | 310 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(307): Show |
323 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1078-5113dupC | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979500 | |||||||
| chr1:70979531 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0219 |
2 | NA19075.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1078-5143A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979531 | |||||||
| chr1:70979552 | T | C | 2 | a0001c0001t0002g0079 a0001c0001t0002g0191 |
2 | HG00438.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1078-5164A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979552 | |||||||
| chr1:70979561 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1078-5173C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979561 | |||||||
| chr1:70979565 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0112 a0001c0001t0001g0254 |
3 | HG01069.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1078-5177C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979565 | |||||||
| chr1:70979587 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1078-5199G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979587 | |||||||
| chr1:70979647 | C | A | 2 | a0001c0001t0001g0314 a0001c0001t0002g0315 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-5259G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979647 | |||||||
| chr1:70979707 | T | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-5319A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979707 | |||||||
| chr1:70979849 | C | T | 10 | a0001c0001t0001g0106 a0001c0002t0001g0328 a0001c0002t0001g0329 others(7): Show |
10 | HG01074.hp1 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-5461G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979849 | |||||||
| chr1:70979961 | T | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1078-5573A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979961 | |||||||
| chr1:70980044 | AG | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-5657delC | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980044 | |||||||
| chr1:70980082 | AAAG | A | 9 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(6): Show |
9 | HG01192.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078-5697_1078-569 others(7): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980082 | |||||||
| chr1:70980104 | G | A | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-5716C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980104 | |||||||
| chr1:70980220 | G | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
106 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1078-5832C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980220 | |||||||
| chr1:70980281 | G | A | 2 | a0001c0001t0001g0314 a0001c0001t0002g0315 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-5893C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980281 | |||||||
| chr1:70980430 | G | A | 11 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0194 others(8): Show |
11 | HG01891.hp1 HG01934.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078-6042C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980430 | |||||||
| chr1:70980451 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1078-6063G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980451 | |||||||
| chr1:70980613 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1078-6225C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980613 | |||||||
| chr1:70980670 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-6282T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980670 | |||||||
| chr1:70980768 | T | C | 1 | a0001c0001t0002g0049 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1078-6380A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980768 | |||||||
| chr1:70980943 | G | A | 4 | a0001c0001t0002g0301 a0001c0001t0002g0303 a0001c0001t0002g0306 others(1): Show |
4 | HG01109.hp1 HG01175.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-6555C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980943 | |||||||
| chr1:70981251 | CT | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0090 a0001c0001t0001g0127 others(3): Show |
6 | HG00639.hp2 HG01074.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-6864delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981251 | |||||||
| chr1:70981259 | TCTTTTCT others(5): Show |
T | 1 | a0001c0001t0002g0098 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1078-6883_1078-687 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981259 | |||||||
| chr1:70981291 | TCTTC | T | 3 | a0001c0001t0001g0208 a0001c0001t0002g0114 a0001c0002t0001g0320 |
3 | HG02965.hp2 HG04184.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1078-6907_1078-690 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981291 | |||||||
| chr1:70981291 | TCTTCCTT others(1): Show |
T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0145 others(4): Show |
8 | HG00639.hp1 HG01255.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-6911_1078-690 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981291 | |||||||
| chr1:70981311 | C | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(195): Show |
204 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1078-6923G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981311 | |||||||
| chr1:70981312 | CTTCCTTT others(5): Show |
C | 16 | a0001c0001t0001g0038 a0001c0001t0001g0119 a0001c0001t0001g0143 others(13): Show |
16 | HG00280.hp1 HG00423.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078-6936_1078-692 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(9): Show |
C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0055 others(41): Show |
46 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1078-6940_1078-692 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(13): Show |
C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0064 others(46): Show |
52 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1078-6944_1078-692 others(24): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(17): Show |
C | 37 | a0001c0001t0001g0057 a0001c0001t0001g0063 a0001c0001t0001g0087 others(34): Show |
37 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1078-6948_1078-692 others(28): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(21): Show |
C | 17 | a0001c0001t0001g0134 a0001c0001t0001g0139 a0001c0001t0002g0034 others(14): Show |
17 | HG00438.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078-6952_1078-692 others(32): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(25): Show |
C | 18 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0182 others(15): Show |
18 | HG00544.hp1 HG00609.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.1078-6956_1078-692 others(36): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(29): Show |
C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0077 a0001c0001t0002g0003 others(10): Show |
14 | HG01109.hp1 HG01175.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078-6960_1078-692 others(40): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(33): Show |
C | 1 | a0001c0001t0002g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1078-6964_1078-692 others(44): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981312 | CTTCCTTT others(37): Show |
C | 1 | a0001c0001t0002g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1078-6968_1078-692 others(48): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981312 | |||||||
| chr1:70981315 | C | T | 1 | a0001c0004t0002g0339 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1078-6927G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981315 | |||||||
| chr1:70981315 | CCTTTCTT others(14): Show |
C | 1 | a0001c0001t0002g0027 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1078-6948_1078-692 others(25): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981315 | |||||||
| chr1:70981316 | CTTTCTTC others(9): Show |
C | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1078-6944_1078-692 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981316 | |||||||
| chr1:70981316 | CTTTCTTC others(17): Show |
C | 1 | a0001c0004t0002g0339 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1078-6952_1078-692 others(28): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981316 | |||||||
| chr1:70981316 | CTTTCTTC others(21): Show |
C | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1078-6956_1078-692 others(32): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981316 | |||||||
| chr1:70981319 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1078-6931A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981319 | |||||||
| chr1:70981320 | C | CTTCT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0091 |
3 | HG00323.hp2 NA18950.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1078-6936_1078-693 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981320 | |||||||
| chr1:70981320 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1078-6932G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981320 | |||||||
| chr1:70981320 | CTTCT | C | 7 | a0001c0001t0001g0085 a0001c0001t0001g0093 a0001c0001t0001g0136 others(4): Show |
8 | HG00140.hp1 HG01255.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-6936_1078-693 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981320 | |||||||
| chr1:70981320 | CTTCTTTC others(1): Show |
C | 5 | a0001c0001t0001g0218 a0001c0002t0001g0330 a0001c0002t0001g0331 others(2): Show |
5 | HG02145.hp1 HG02258.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-6940_1078-693 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981320 | |||||||
| chr1:70981320 | CTTCTTTC others(5): Show |
C | 3 | a0001c0002t0001g0327 a0001c0002t0001g0329 a0001c0002t0001g0334 |
3 | HG02809.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1078-6944_1078-693 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981320 | |||||||
| chr1:70981320 | CTTCTTTC others(9): Show |
C | 2 | a0001c0002t0001g0335 a0001c0004t0002g0338 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1078-6948_1078-693 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981320 | |||||||
| chr1:70981320 | CTTCTTTC others(13): Show |
C | 5 | a0001c0001t0001g0106 a0001c0004t0002g0340 a0001c0004t0002g0341 others(2): Show |
5 | HG03041.hp1 HG03209.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-6952_1078-693 others(24): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981320 | |||||||
| chr1:70981323 | CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1078-6952_1078-693 others(21): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981323 | |||||||
| chr1:70981356 | TTTCTTTC others(41): Show |
T | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-7016_1078-696 others(52): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981356 | |||||||
| chr1:70981368 | TTTCTTTC others(33): Show |
T | 1 | a0005c0006t0001g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1078-7020_1078-698 others(44): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981368 | |||||||
| chr1:70981372 | TTTCTTTC others(17): Show |
T | 1 | a0001c0001t0001g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1078-7008_1078-698 others(28): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981372 | |||||||
| chr1:70981372 | TTTCTTTC others(25): Show |
T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0065 a0001c0001t0001g0203 |
4 | HG00423.hp2 HG01515.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-7016_1078-698 others(36): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981372 | |||||||
| chr1:70981375 | CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0002g0033 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1078-7004_1078-698 others(21): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981375 | |||||||
| chr1:70981376 | TTTCTTTC others(13): Show |
T | 1 | a0001c0001t0001g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1078-7008_1078-698 others(24): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981376 | |||||||
| chr1:70981376 | TTTCTTTC others(17): Show |
T | 1 | a0001c0001t0001g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1078-7012_1078-698 others(28): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981376 | |||||||
| chr1:70981376 | TTTCTTTC others(21): Show |
T | 6 | a0001c0001t0001g0066 a0001c0001t0001g0217 a0001c0001t0001g0237 others(3): Show |
6 | HG00544.hp2 HG02015.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-7016_1078-698 others(32): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981376 | |||||||
| chr1:70981376 | TTTCTTTC others(25): Show |
T | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01192.hp2 HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1078-7020_1078-698 others(36): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981376 | |||||||
| chr1:70981380 | TTTCTTTC others(9): Show |
T | 1 | a0001c0001t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1078-7008_1078-699 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981380 | |||||||
| chr1:70981380 | TTTCTTTC others(17): Show |
T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0018 others(8): Show |
11 | HG00323.hp1 HG00609.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078-7016_1078-699 others(28): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981380 | |||||||
| chr1:70981380 | TTTCTTTC others(21): Show |
T | 3 | a0001c0002t0001g0320 a0001c0002t0001g0321 a0001c0002t0006g0326 |
3 | HG02451.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1078-7020_1078-699 others(32): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981380 | |||||||
| chr1:70981382 | TCTTTCTT others(10): Show |
T | 1 | a0001c0001t0001g0221 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1078-7011_1078-699 others(21): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981382 | |||||||
| chr1:70981384 | T | C | 3 | a0001c0001t0005g0107 a0001c0002t0001g0325 a0003c0005t0002g0290 |
3 | HG00639.hp2 HG01346.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1078-6996A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981384 | |||||||
| chr1:70981384 | TTTCTTTC others(5): Show |
T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG01255.hp1 HG02602.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-7008_1078-699 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981384 | |||||||
| chr1:70981384 | TTTCTTTC others(9): Show |
T | 3 | a0001c0001t0001g0213 a0001c0001t0001g0269 a0001c0001t0001g0308 |
3 | HG01346.hp1 HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1078-7012_1078-699 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981384 | |||||||
| chr1:70981384 | TTTCTTTC others(13): Show |
T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0025 others(10): Show |
14 | HG00673.hp1 HG01106.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078-7016_1078-699 others(24): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981384 | |||||||
| chr1:70981384 | TTTCTTTC others(17): Show |
T | 2 | a0001c0002t0001g0319 a0001c0002t0001g0322 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1078-7020_1078-699 others(28): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981384 | |||||||
| chr1:70981388 | T | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0022 others(15): Show |
20 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1078-7000A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981388 | |||||||
| chr1:70981388 | TTTCTTTC others(1): Show |
T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0002t0001g0328 |
5 | HG00738.hp2 HG01074.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-7008_1078-700 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981388 | |||||||
| chr1:70981388 | TTTCTTTC others(5): Show |
T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0225 |
2 | NA19090.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1078-7012_1078-700 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981388 | |||||||
| chr1:70981388 | TTTCTTTC others(9): Show |
T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0196 others(16): Show |
19 | HG00642.hp2 HG00741.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1078-7016_1078-700 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981388 | |||||||
| chr1:70981392 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1078-7004A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981392 | |||||||
| chr1:70981392 | TTTCC | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0072 others(4): Show |
7 | HG01071.hp1 NA18965.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-7008_1078-700 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981392 | |||||||
| chr1:70981392 | TTTCCTTC others(1): Show |
T | 13 | a0001c0001t0001g0019 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
13 | HG01496.hp1 HG02056.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-7012_1078-700 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981392 | |||||||
| chr1:70981392 | TTTCCTTC others(5): Show |
T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(8): Show |
11 | HG00621.hp1 HG01943.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.1078-7016_1078-700 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981392 | |||||||
| chr1:70981392 | TTTCCTTC others(9): Show |
T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1078-7020_1078-700 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981392 | |||||||
| chr1:70981396 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0091 others(10): Show |
15 | HG00323.hp2 HG01069.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.1078-7008G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981396 | |||||||
| chr1:70981399 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1078-7011G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981399 | |||||||
| chr1:70981400 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0001g0200 others(6): Show |
9 | HG01993.hp2 NA18965.hp2 NA18985.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078-7012G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981400 | |||||||
| chr1:70981403 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1078-7015G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981403 | |||||||
| chr1:70981404 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0070 others(18): Show |
21 | HG01496.hp1 HG01993.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.1078-7016G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981404 | |||||||
| chr1:70981421 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1078-7033A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981421 | |||||||
| chr1:70981466 | C | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(304): Show |
320 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1078-7078G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981466 | |||||||
| chr1:70981548 | A | G | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-7160T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981548 | |||||||
| chr1:70981687 | G | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-7299C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981687 | |||||||
| chr1:70981762 | T | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-7374A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981762 | |||||||
| chr1:70981836 | A | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1078-7448T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981836 | |||||||
| chr1:70981889 | C | T | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-7501G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981889 | |||||||
| chr1:70982056 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-7668C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982056 | |||||||
| chr1:70982110 | G | C | 306 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(303): Show |
319 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.1078-7722C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982110 | |||||||
| chr1:70982174 | A | C | 1 | a0001c0001t0002g0130 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1078-7786T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982174 | |||||||
| chr1:70982186 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1078-7798A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982186 | |||||||
| chr1:70982300 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1078-7912C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982300 | |||||||
| chr1:70982421 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-8033G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982421 | |||||||
| chr1:70982562 | T | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-8174A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982562 | |||||||
| chr1:70982589 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1078-8201T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982589 | |||||||
| chr1:70982680 | T | C | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(5): Show |
8 | HG01192.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1078-8292A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982680 | |||||||
| chr1:70982783 | T | G | 7 | a0001c0001t0001g0136 a0001c0001t0001g0218 a0001c0002t0001g0016 others(4): Show |
8 | HG00099.hp1 HG00140.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-8395A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982783 | |||||||
| chr1:70982785 | T | C | 3 | a0001c0001t0002g0295 a0001c0001t0002g0297 a0001c0001t0002g0317 |
3 | HG02055.hp1 HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1078-8397A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982785 | |||||||
| chr1:70982794 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1078-8406A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982794 | |||||||
| chr1:70982866 | A | C | 1 | a0001c0001t0003g0346 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1078-8478T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982866 | |||||||
| chr1:70982931 | A | G | 16 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0002g0298 others(13): Show |
16 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078-8543T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982931 | |||||||
| chr1:70982968 | A | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-8580T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70982968 | |||||||
| chr1:70983023 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1078-8635G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983023 | |||||||
| chr1:70983064 | C | A | 1 | a0001c0002t0001g0328 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1078-8676G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983064 | |||||||
| chr1:70983096 | G | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1078-8708C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983096 | |||||||
| chr1:70983215 | T | C | 87 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(84): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1078-8827A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983215 | |||||||
| chr1:70983243 | A | G | 2 | a0001c0001t0001g0314 a0001c0001t0002g0315 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-8855T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983243 | |||||||
| chr1:70983284 | G | GAAA | 200 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1078-8899_1078-889 others(7): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983284 | |||||||
| chr1:70983298 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
92 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1078-8910G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983298 | |||||||
| chr1:70983447 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1078-9059A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983447 | |||||||
| chr1:70983757 | TTG | T | 87 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(84): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1078-9371_1078-937 others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983757 | |||||||
| chr1:70983797 | C | CT | 4 | a0001c0001t0001g0314 a0001c0001t0002g0315 a0003c0005t0002g0289 others(1): Show |
4 | HG00639.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-9410dupA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983797 | |||||||
| chr1:70983817 | C | T | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1078-9429G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983817 | |||||||
| chr1:70983851 | C | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG01192.hp2 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-9463G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983851 | |||||||
| chr1:70983987 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1078-9599G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983987 | |||||||
| chr1:70984129 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-9741C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984129 | |||||||
| chr1:70984202 | C | T | 1 | a0001c0002t0010g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1078-9814G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984202 | |||||||
| chr1:70984261 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1078-9873G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984261 | |||||||
| chr1:70984302 | G | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
103 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1078-9914C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984302 | |||||||
| chr1:70984386 | CA | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1078-9999delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984386 | |||||||
| chr1:70984451 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1078-10063T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984451 | |||||||
| chr1:70984594 | C | T | 8 | a0001c0001t0002g0026 a0001c0001t0002g0036 a0001c0001t0002g0056 others(5): Show |
8 | HG02083.hp2 NA18948.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-10206G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984594 | |||||||
| chr1:70984727 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1078-10339A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984727 | |||||||
| chr1:70984740 | A | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0264 a0001c0001t0002g0032 others(1): Show |
4 | NA18939.hp2 NA19064.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-10352T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984740 | |||||||
| chr1:70984844 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1078-10456C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984844 | |||||||
| chr1:70985077 | C | A | 1 | a0001c0001t0002g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1078-10689G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70985077 | |||||||
| chr1:70985080 | C | G | 87 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(84): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1078-10692G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70985080 | |||||||
| chr1:70985184 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0260 |
2 | HG00280.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1078-10796C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70985184 | |||||||
| chr1:70985325 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1078-10937G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70985325 | |||||||
| chr1:70985408 | A | G | 120 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0029 others(117): Show |
122 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1078-11020T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70985408 | |||||||
| chr1:70985639 | C | T | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-11251G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70985639 | |||||||
| chr1:70985643 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1078-11255T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70985643 | |||||||
| chr1:70986011 | G | C | 2 | a0001c0001t0001g0314 a0001c0001t0002g0315 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-11623C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70986011 | |||||||
| chr1:70986441 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1078-12053G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70986441 | |||||||
| chr1:70986697 | G | T | 1 | a0001c0001t0001g0244 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1078-12309C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70986697 | |||||||
| chr1:70986723 | A | G | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-12335T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70986723 | |||||||
| chr1:70986874 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1078-12486C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70986874 | |||||||
| chr1:70986886 | A | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
92 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1078-12498T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70986886 | |||||||
| chr1:70987313 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1078-12925T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987313 | |||||||
| chr1:70987366 | T | G | 1 | a0001c0001t0002g0098 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1078-12978A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987366 | |||||||
| chr1:70987419 | A | T | 5 | a0001c0001t0001g0113 a0001c0001t0001g0126 a0001c0001t0001g0134 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-13031T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987419 | |||||||
| chr1:70987440 | C | A | 1 | a0001c0002t0010g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1078-13052G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987440 | |||||||
| chr1:70987487 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1078-13099T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987487 | |||||||
| chr1:70987536 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-13148G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987536 | |||||||
| chr1:70987544 | A | G | 8 | a0001c0001t0001g0136 a0001c0001t0001g0218 a0001c0002t0001g0016 others(5): Show |
9 | HG00099.hp1 HG00140.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-13156T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987544 | |||||||
| chr1:70987761 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
5 | HG02132.hp1 NA18950.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-13373T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987761 | |||||||
| chr1:70987852 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0002g0315 |
3 | HG03209.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-13464A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987852 | |||||||
| chr1:70987868 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-13480G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987868 | |||||||
| chr1:70987869 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.1078-13481T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987869 | |||||||
| chr1:70987984 | T | A | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1078-13596A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70987984 | |||||||
| chr1:70988208 | G | A | 94 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(91): Show |
95 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.1078-13820C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988208 | |||||||
| chr1:70988326 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1078-13938G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988326 | |||||||
| chr1:70988393 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1078-14005G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988393 | |||||||
| chr1:70988654 | A | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-14266T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988654 | |||||||
| chr1:70988669 | C | T | 87 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(84): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1078-14281G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988669 | |||||||
| chr1:70988690 | A | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
92 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1078-14302T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988690 | |||||||
| chr1:70988792 | A | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1078-14404T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988792 | |||||||
| chr1:70988872 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1078-14484T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988872 | |||||||
| chr1:70988941 | C | T | 8 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(5): Show |
8 | HG01192.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1078-14553G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988941 | |||||||
| chr1:70988973 | G | T | 1 | a0001c0001t0008g0141 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1078-14585C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988973 | |||||||
| chr1:70989033 | C | A | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1078-14645G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989033 | |||||||
| chr1:70989035 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-14647G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989035 | |||||||
| chr1:70989038 | C | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0002g0315 |
3 | HG03209.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-14650G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989038 | |||||||
| chr1:70989040 | C | G | 1 | a0001c0001t0002g0309 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1078-14652G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989040 | |||||||
| chr1:70989127 | C | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-14739G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989127 | |||||||
| chr1:70989131 | C | T | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1078-14743G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989131 | |||||||
| chr1:70989186 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1078-14798C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989186 | |||||||
| chr1:70989284 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1078-14896C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989284 | |||||||
| chr1:70989367 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0186 |
2 | NA18957.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1078-14979A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989367 | |||||||
| chr1:70989376 | G | A | 1 | a0006c0008t0002g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1078-14988C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989376 | |||||||
| chr1:70989452 | T | C | 9 | a0001c0001t0001g0085 a0001c0001t0001g0136 a0001c0001t0001g0218 others(6): Show |
10 | HG00099.hp1 HG00140.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1078-15064A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989452 | |||||||
| chr1:70989694 | G | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-15306C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989694 | |||||||
| chr1:70989787 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(212): Show |
222 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1078-15399A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989787 | |||||||
| chr1:70989896 | C | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-15508G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70989896 | |||||||
| chr1:70990058 | A | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-15670T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990058 | |||||||
| chr1:70990140 | T | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0216 |
2 | NA18994.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1078-15752A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990140 | |||||||
| chr1:70990156 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1078-15768T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990156 | |||||||
| chr1:70990169 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1078-15781G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990169 | |||||||
| chr1:70990218 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1078-15830C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990218 | |||||||
| chr1:70990225 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1078-15837G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990225 | |||||||
| chr1:70990289 | G | A | 7 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(4): Show |
7 | HG01255.hp1 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-15901C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990289 | |||||||
| chr1:70990313 | C | T | 1 | a0006c0008t0002g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1078-15925G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990313 | |||||||
| chr1:70990335 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-15947G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990335 | |||||||
| chr1:70990353 | T | TCA | 76 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0013 others(73): Show |
80 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1078-15967_1078-15 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990353 | |||||||
| chr1:70990353 | T | TCACA | 20 | a0001c0001t0001g0085 a0001c0001t0001g0136 a0001c0001t0001g0196 others(17): Show |
20 | HG00140.hp1 HG03490.hp2 HG04184.hp1 others(17): Show |
intron_variant | MODIFIER | c.1078-15969_1078-15 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990353 | |||||||
| chr1:70990353 | T | TCACACA | 2 | a0001c0001t0001g0012 a0001c0001t0001g0228 |
3 | HG01943.hp2 HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1078-15971_1078-15 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990353 | |||||||
| chr1:70990353 | TCA | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0002c0003t0001g0226 |
3 | HG02559.hp2 HG02622.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1078-15967_1078-15 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990353 | |||||||
| chr1:70990353 | TCACACAC others(1): Show |
T | 7 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0002g0028 others(4): Show |
7 | HG00609.hp2 NA18949.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-15973_1078-15 others(14): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990353 | |||||||
| chr1:70990384 | C | T | 12 | a0001c0001t0001g0024 a0001c0001t0001g0106 a0001c0001t0002g0023 others(9): Show |
12 | HG00609.hp2 HG03453.hp1 HG03579.hp1 others(9): Show |
intron_variant | MODIFIER | c.1078-15996G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990384 | |||||||
| chr1:70990386 | C | CACAT | 9 | a0001c0001t0001g0233 a0001c0001t0002g0108 a0001c0004t0002g0338 others(6): Show |
9 | HG00735.hp1 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1078-15999_1078-15 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990386 | |||||||
| chr1:70990386 | C | CACATAT | 9 | a0001c0001t0002g0026 a0001c0001t0002g0105 a0001c0001t0002g0292 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-15999_1078-15 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990386 | |||||||
| chr1:70990386 | C | CAT | 19 | a0001c0001t0002g0030 a0001c0001t0002g0097 a0001c0001t0002g0104 others(16): Show |
19 | HG00544.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1078-16000_1078-15 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990386 | |||||||
| chr1:70990386 | C | CATAT | 38 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0053 others(35): Show |
39 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1078-16002_1078-15 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990386 | |||||||
| chr1:70990386 | C | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0106 a0001c0001t0001g0314 others(13): Show |
16 | HG00609.hp2 HG02258.hp1 HG03209.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078-15998G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990386 | |||||||
| chr1:70990386 | CAT | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1078-16000_1078-15 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990386 | |||||||
| chr1:70990388 | T | C | 15 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0077 others(12): Show |
16 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078-16000A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990388 | |||||||
| chr1:70990390 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1078-16002A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990390 | |||||||
| chr1:70990400 | T | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-16012A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990400 | |||||||
| chr1:70990402 | A | T | 1 | a0001c0001t0002g0202 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1078-16014T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990402 | |||||||
| chr1:70990442 | AAT | A | 187 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
194 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.1078-16056_1078-16 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990442 | |||||||
| chr1:70990442 | AATAT | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-16058_1078-16 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990442 | |||||||
| chr1:70990480 | A | G | 1 | a0001c0001t0003g0350 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1078-16092T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990480 | |||||||
| chr1:70990807 | T | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1078-16419A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990807 | |||||||
| chr1:70990831 | A | G | 2 | a0001c0001t0002g0076 a0006c0008t0002g0043 |
2 | NA18956.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1078-16443T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990831 | |||||||
| chr1:70990985 | A | G | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1078-16597T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70990985 | |||||||
| chr1:70991061 | T | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0002g0315 |
3 | HG03209.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1078-16673A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991061 | |||||||
| chr1:70991260 | C | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-16872G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991260 | |||||||
| chr1:70991433 | A | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-17045T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991433 | |||||||
| chr1:70991513 | A | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0195 |
2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1078-17125T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991513 | |||||||
| chr1:70991627 | G | A | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-17239C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991627 | |||||||
| chr1:70991872 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1078-17484G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991872 | |||||||
| chr1:70991901 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1078-17513A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991901 | |||||||
| chr1:70991978 | A | C | 6 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG00621.hp1 HG02155.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-17590T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70991978 | |||||||
| chr1:70992128 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-17740G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992128 | |||||||
| chr1:70992154 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1078-17766C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992154 | |||||||
| chr1:70992258 | C | T | 336 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1078-17870G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992258 | |||||||
| chr1:70992291 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1078-17903A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992291 | |||||||
| chr1:70992291 | T | G | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1078-17903A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992291 | |||||||
| chr1:70992414 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-18026T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992414 | |||||||
| chr1:70992458 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1078-18070G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992458 | |||||||
| chr1:70992460 | A | G | 13 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
13 | HG00140.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-18072T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992460 | |||||||
| chr1:70992479 | T | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
109 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1078-18091A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992479 | |||||||
| chr1:70992665 | A | G | 95 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(92): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1078-18277T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992665 | |||||||
| chr1:70992711 | C | T | 12 | a0001c0001t0001g0073 a0001c0001t0001g0211 a0001c0001t0001g0233 others(9): Show |
12 | HG00621.hp1 HG02155.hp2 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.1078-18323G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992711 | |||||||
| chr1:70992725 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1078-18337A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70992725 | |||||||
| chr1:70993043 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1078-18655G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993043 | |||||||
| chr1:70993129 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1078-18741A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993129 | |||||||
| chr1:70993175 | T | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1078-18787A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993175 | |||||||
| chr1:70993365 | G | C | 310 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(307): Show |
323 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1077+18940C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993365 | |||||||
| chr1:70993367 | G | A | 95 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(92): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1077+18938C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993367 | |||||||
| chr1:70993368 | C | T | 95 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(92): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1077+18937G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993368 | |||||||
| chr1:70993568 | T | C | 6 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0002g0315 others(3): Show |
6 | HG00639.hp2 HG02572.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+18737A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993568 | |||||||
| chr1:70993598 | T | C | 1 | a0001c0002t0001g0330 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1077+18707A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993598 | |||||||
| chr1:70993756 | G | A | 9 | a0001c0002t0001g0328 a0001c0002t0001g0329 a0001c0002t0001g0330 others(6): Show |
9 | HG01074.hp1 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077+18549C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993756 | |||||||
| chr1:70993958 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0260 |
2 | HG00280.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1077+18347C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993958 | |||||||
| chr1:70994092 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1077+18213T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994092 | |||||||
| chr1:70994124 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1077+18181G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994124 | |||||||
| chr1:70994313 | G | A | 7 | a0001c0001t0001g0077 a0001c0001t0001g0230 a0001c0001t0001g0231 others(4): Show |
7 | HG00140.hp2 HG01433.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077+17992C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994313 | |||||||
| chr1:70994420 | T | C | 8 | a0001c0001t0002g0108 a0001c0001t0003g0345 a0001c0001t0003g0346 others(5): Show |
8 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+17885A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994420 | |||||||
| chr1:70994461 | A | AT | 202 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1077+17843dupA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994461 | |||||||
| chr1:70994496 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1077+17809G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994496 | |||||||
| chr1:70994542 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1077+17763G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994542 | |||||||
| chr1:70994650 | G | A | 15 | a0001c0001t0002g0288 a0001c0001t0002g0298 a0001c0001t0002g0299 others(12): Show |
15 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1077+17655C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994650 | |||||||
| chr1:70994693 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1077+17612G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994693 | |||||||
| chr1:70994801 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1077+17504G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994801 | |||||||
| chr1:70994810 | T | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1077+17495A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994810 | |||||||
| chr1:70994832 | C | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0185 |
2 | NA18959.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1077+17473G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994832 | |||||||
| chr1:70995058 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1077+17247C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70995058 | |||||||
| chr1:70995253 | G | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
109 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1077+17052C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70995253 | |||||||
| chr1:70995629 | T | G | 13 | a0001c0001t0001g0308 a0001c0001t0002g0288 a0001c0001t0002g0301 others(10): Show |
13 | HG01071.hp2 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1077+16676A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70995629 | |||||||
| chr1:70995642 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+16663C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70995642 | |||||||
| chr1:70995923 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1077+16382G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70995923 | |||||||
| chr1:70996026 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+16279T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996026 | |||||||
| chr1:70996307 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1077+15998T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996307 | |||||||
| chr1:70996561 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1077+15744A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996561 | |||||||
| chr1:70996567 | T | A | 1 | a0001c0001t0002g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1077+15738A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996567 | |||||||
| chr1:70996585 | C | T | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1077+15720G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996585 | |||||||
| chr1:70996617 | T | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18999.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1077+15688A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996617 | |||||||
| chr1:70996618 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18999.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1077+15687C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996618 | |||||||
| chr1:70996637 | AT | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
68 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1077+15667delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996637 | |||||||
| chr1:70996638 | TTTTTA | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0168 a0001c0001t0001g0279 others(2): Show |
6 | HG01192.hp2 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+15662_1077+15 others(11): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996638 | |||||||
| chr1:70996639 | T | TTTA | 25 | a0001c0001t0001g0169 a0001c0001t0001g0196 a0001c0001t0001g0208 others(22): Show |
25 | HG00639.hp2 HG01069.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1077+15665_1077+15 others(9): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTATTTA | 7 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0210 others(4): Show |
7 | HG00673.hp1 HG02257.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+15665_1077+15 others(13): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTATTTA others(4): Show |
4 | a0001c0001t0001g0167 a0001c0001t0001g0269 a0001c0001t0002g0315 others(1): Show |
4 | HG03453.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+15665_1077+15 others(17): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTATTTA others(8): Show |
1 | a0001c0001t0001g0274 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077+15665_1077+15 others(21): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTA | 8 | a0001c0001t0001g0057 a0001c0001t0001g0082 a0001c0001t0001g0093 others(5): Show |
8 | HG00438.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077+15662_1077+15 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTATTT others(1): Show |
51 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0064 others(48): Show |
53 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1077+15658_1077+15 others(14): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTATTT others(5): Show |
91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(88): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1077+15654_1077+15 others(18): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTATTT others(9): Show |
53 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0088 others(50): Show |
54 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1077+15650_1077+15 others(22): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTATTT others(13): Show |
15 | a0001c0001t0001g0063 a0001c0001t0001g0131 a0001c0001t0001g0193 others(12): Show |
15 | HG00408.hp1 HG02055.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1077+15646_1077+15 others(26): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTATTT others(17): Show |
3 | a0001c0001t0001g0110 a0001c0001t0001g0123 a0001c0001t0001g0182 |
3 | HG00735.hp2 HG01884.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1077+15642_1077+15 others(30): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTTATT others(10): Show |
1 | a0001c0001t0001g0181 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1077+15665_1077+15 others(23): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTTTAA others(8): Show |
1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1077+15665_1077+15 others(21): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996639 | T | TTTTTTAA others(12): Show |
1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1077+15665_1077+15 others(25): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996639 | |||||||
| chr1:70996880 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1077+15425A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996880 | |||||||
| chr1:70996913 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1077+15392A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996913 | |||||||
| chr1:70996921 | A | C | 1 | a0001c0001t0001g0213 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1077+15384T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996921 | |||||||
| chr1:70996951 | T | C | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077+15354A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996951 | |||||||
| chr1:70996954 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+15351C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996954 | |||||||
| chr1:70996979 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1077+15326C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70996979 | |||||||
| chr1:70997132 | C | T | 7 | a0001c0001t0003g0345 a0001c0001t0003g0346 a0001c0001t0003g0347 others(4): Show |
7 | HG00280.hp2 HG00741.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+15173G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997132 | |||||||
| chr1:70997133 | T | G | 107 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(104): Show |
113 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1077+15172A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997133 | |||||||
| chr1:70997176 | G | A | 1 | a0001c0002t0001g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1077+15129C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997176 | |||||||
| chr1:70997273 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1077+15032T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997273 | |||||||
| chr1:70997324 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1077+14981C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997324 | |||||||
| chr1:70997552 | C | T | 4 | a0001c0002t0001g0329 a0001c0002t0001g0330 a0001c0002t0001g0331 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+14753G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997552 | |||||||
| chr1:70997585 | A | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
102 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1077+14720T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997585 | |||||||
| chr1:70997807 | G | C | 330 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(327): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1077+14498C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997807 | |||||||
| chr1:70997865 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1077+14440G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997865 | |||||||
| chr1:70997935 | A | C | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077+14370T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70997935 | |||||||
| chr1:70998000 | C | G | 1 | a0001c0001t0001g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1077+14305G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998000 | |||||||
| chr1:70998130 | C | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+14175G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998130 | |||||||
| chr1:70998245 | G | A | 1 | a0001c0002t0001g0016 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1077+14060C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998245 | |||||||
| chr1:70998287 | G | C | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG01192.hp2 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+14018C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998287 | |||||||
| chr1:70998362 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1077+13943C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998362 | |||||||
| chr1:70998407 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+13898G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998407 | |||||||
| chr1:70998634 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+13671C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998634 | |||||||
| chr1:70998710 | T | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+13595A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998710 | |||||||
| chr1:70998722 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+13583G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998722 | |||||||
| chr1:70998738 | G | A | 1 | a0001c0001t0003g0345 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1077+13567C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998738 | |||||||
| chr1:70998781 | A | C | 4 | a0001c0002t0001g0319 a0001c0002t0001g0320 a0001c0002t0001g0321 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+13524T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998781 | |||||||
| chr1:70998811 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1077+13494C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998811 | |||||||
| chr1:70998845 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1077+13460C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998845 | |||||||
| chr1:70998865 | C | T | 332 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1077+13440G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998865 | |||||||
| chr1:70998969 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1077+13336G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998969 | |||||||
| chr1:70998997 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1077+13308G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70998997 | |||||||
| chr1:70999036 | C | T | 96 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(93): Show |
97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1077+13269G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999036 | |||||||
| chr1:70999114 | T | G | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1077+13191A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999114 | |||||||
| chr1:70999263 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1077+13042T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999263 | |||||||
| chr1:70999489 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1077+12816G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999489 | |||||||
| chr1:70999523 | A | C | 331 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1077+12782T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999523 | |||||||
| chr1:70999609 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1077+12696T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999609 | |||||||
| chr1:70999715 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0053 a0001c0001t0001g0279 others(1): Show |
5 | HG02109.hp1 HG02615.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077+12590G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999715 | |||||||
| chr1:71000092 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+12213A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71000092 | |||||||
| chr1:71000355 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1077+11950A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71000355 | |||||||
| chr1:71000950 | G | A | 96 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1077+11355C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71000950 | |||||||
| chr1:71000961 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1077+11344A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71000961 | |||||||
| chr1:71001017 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1077+11288C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001017 | |||||||
| chr1:71001018 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1077+11287C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001018 | |||||||
| chr1:71001195 | AAACTT | A | 16 | a0001c0001t0001g0308 a0001c0001t0002g0288 a0001c0001t0002g0298 others(13): Show |
16 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1077+11105_1077+11 others(11): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001195 | |||||||
| chr1:71001198 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1077+11107G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001198 | |||||||
| chr1:71001236 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+11069A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001236 | |||||||
| chr1:71001490 | A | G | 1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1077+10815T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001490 | |||||||
| chr1:71001552 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0274 a0001c0001t0001g0276 others(1): Show |
4 | HG02257.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+10753C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001552 | |||||||
| chr1:71001571 | GT | G | 8 | a0001c0001t0002g0108 a0001c0001t0003g0345 a0001c0001t0003g0346 others(5): Show |
8 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+10733delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001571 | |||||||
| chr1:71001794 | C | T | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+10511G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001794 | |||||||
| chr1:71001979 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1077+10326C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71001979 | |||||||
| chr1:71002357 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1077+9948A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71002357 | |||||||
| chr1:71002626 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077+9679C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71002626 | |||||||
| chr1:71002769 | G | T | 331 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1077+9536C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71002769 | |||||||
| chr1:71002810 | A | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.1077+9495T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71002810 | |||||||
| chr1:71002819 | C | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+9486G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71002819 | |||||||
| chr1:71002873 | C | G | 1 | a0001c0001t0001g0022 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1077+9432G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71002873 | |||||||
| chr1:71003086 | T | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18999.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1077+9219A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003086 | |||||||
| chr1:71003115 | A | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+9190T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003115 | |||||||
| chr1:71003192 | G | A | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1077+9113C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003192 | |||||||
| chr1:71003206 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+9099A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003206 | |||||||
| chr1:71003393 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1077+8912T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003393 | |||||||
| chr1:71003423 | T | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
102 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1077+8882A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003423 | |||||||
| chr1:71003529 | A | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+8776T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003529 | |||||||
| chr1:71003802 | C | T | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1077+8503G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003802 | |||||||
| chr1:71003833 | G | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+8472C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003833 | |||||||
| chr1:71003877 | G | A | 46 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(43): Show |
47 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1077+8428C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003877 | |||||||
| chr1:71003888 | T | C | 15 | a0001c0001t0001g0053 a0001c0001t0002g0104 a0001c0001t0002g0105 others(12): Show |
15 | HG01891.hp1 HG01934.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1077+8417A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003888 | |||||||
| chr1:71003900 | G | A | 102 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0029 others(99): Show |
104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1077+8405C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003900 | |||||||
| chr1:71003912 | C | A | 1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1077+8393G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71003912 | |||||||
| chr1:71004056 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1077+8249T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71004056 | |||||||
| chr1:71004076 | T | C | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+8229A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71004076 | |||||||
| chr1:71004136 | C | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(197): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1077+8169G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71004136 | |||||||
| chr1:71004263 | G | A | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1077+8042C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71004263 | |||||||
| chr1:71004325 | A | G | 1 | a0001c0009t0007g0337 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1077+7980T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71004325 | |||||||
| chr1:71004939 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+7366G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71004939 | |||||||
| chr1:71004988 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1077+7317C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71004988 | |||||||
| chr1:71005111 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+7194C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005111 | |||||||
| chr1:71005121 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+7184G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005121 | |||||||
| chr1:71005227 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1077+7078G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005227 | |||||||
| chr1:71005261 | G | A | 8 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0045 others(5): Show |
8 | NA18944.hp2 NA18960.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+7044C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005261 | |||||||
| chr1:71005267 | A | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+7038T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005267 | |||||||
| chr1:71005319 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+6986G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005319 | |||||||
| chr1:71005454 | T | C | 96 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1077+6851A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005454 | |||||||
| chr1:71005455 | G | A | 4 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(1): Show |
4 | HG01192.hp2 HG02257.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+6850C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005455 | |||||||
| chr1:71005632 | T | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0271 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1077+6673A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005632 | |||||||
| chr1:71005684 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1077+6621G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005684 | |||||||
| chr1:71005728 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1077+6577G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71005728 | |||||||
| chr1:71006067 | C | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1077+6238G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006067 | |||||||
| chr1:71006090 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1077+6215T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006090 | |||||||
| chr1:71006098 | G | A | 200 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(197): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1077+6207C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006098 | |||||||
| chr1:71006098 | G | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+6207C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006098 | |||||||
| chr1:71006192 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1077+6113A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006192 | |||||||
| chr1:71006267 | T | C | 334 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(331): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1077+6038A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006267 | |||||||
| chr1:71006273 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1077+6032G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006273 | |||||||
| chr1:71006462 | A | C | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1077+5843T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006462 | |||||||
| chr1:71006463 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1077+5842C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006463 | |||||||
| chr1:71006470 | A | T | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1077+5835T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006470 | |||||||
| chr1:71006550 | C | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+5755G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006550 | |||||||
| chr1:71006678 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+5627G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006678 | |||||||
| chr1:71006695 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1077+5610A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006695 | |||||||
| chr1:71006855 | G | A | 2 | a0001c0001t0002g0302 a0001c0001t0002g0304 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1077+5450C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71006855 | |||||||
| chr1:71007228 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0166 |
6 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+5077C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71007228 | |||||||
| chr1:71007291 | G | C | 1 | a0001c0001t0004g0075 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1077+5014C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71007291 | |||||||
| chr1:71007357 | AT | A | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+4947delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71007357 | |||||||
| chr1:71007556 | T | C | 1 | a0001c0001t0002g0313 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1077+4749A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71007556 | |||||||
| chr1:71008106 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1077+4199A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71008106 | |||||||
| chr1:71008108 | T | C | 97 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(94): Show |
102 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1077+4197A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71008108 | |||||||
| chr1:71008311 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+3994T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71008311 | |||||||
| chr1:71008472 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0059 |
2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1077+3833G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71008472 | |||||||
| chr1:71008558 | G | A | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+3747C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71008558 | |||||||
| chr1:71008762 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1077+3543T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71008762 | |||||||
| chr1:71009041 | T | TA | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+3263dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009041 | |||||||
| chr1:71009099 | A | G | 102 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0029 others(99): Show |
104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1077+3206T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009099 | |||||||
| chr1:71009199 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+3106A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009199 | |||||||
| chr1:71009380 | T | C | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1077+2925A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009380 | |||||||
| chr1:71009412 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+2893T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009412 | |||||||
| chr1:71009590 | T | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1077+2715A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009590 | |||||||
| chr1:71009688 | CT | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+2616delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009688 | |||||||
| chr1:71009964 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+2341T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71009964 | |||||||
| chr1:71010027 | C | T | 102 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0029 others(99): Show |
104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1077+2278G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71010027 | |||||||
| chr1:71010185 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1077+2120C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71010185 | |||||||
| chr1:71010502 | C | T | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1077+1803G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71010502 | |||||||
| chr1:71010535 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1077+1770T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71010535 | |||||||
| chr1:71010600 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1077+1705C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71010600 | |||||||
| chr1:71010763 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1077+1542G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71010763 | |||||||
| chr1:71010868 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077+1437T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71010868 | |||||||
| chr1:71011004 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1077+1301T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011004 | |||||||
| chr1:71011078 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1077+1227C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011078 | |||||||
| chr1:71011079 | G | T | 4 | a0001c0002t0001g0329 a0001c0002t0001g0330 a0001c0002t0001g0331 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+1226C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011079 | |||||||
| chr1:71011089 | A | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0274 a0001c0001t0001g0276 others(1): Show |
4 | HG02257.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+1216T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011089 | |||||||
| chr1:71011189 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1077+1116C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011189 | |||||||
| chr1:71011434 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1077+871G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011434 | |||||||
| chr1:71011529 | T | C | 1 | a0001c0002t0010g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1077+776A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011529 | |||||||
| chr1:71011559 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1077+746C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011559 | |||||||
| chr1:71011632 | A | T | 200 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(197): Show |
207 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1077+673T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011632 | |||||||
| chr1:71011697 | A | C | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1077+608T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011697 | |||||||
| chr1:71011715 | A | T | 12 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(9): Show |
13 | HG00099.hp1 HG01255.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1077+590T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011715 | |||||||
| chr1:71011788 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1077+517C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011788 | |||||||
| chr1:71011842 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1077+463T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011842 | |||||||
| chr1:71011856 | A | G | 89 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): Show |
94 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1077+449T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71011856 | |||||||
| chr1:71012136 | C | A | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1077+169G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71012136 | |||||||
| chr1:71012158 | A | T | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.1077+147T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71012158 | |||||||
| chr1:71012531 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.898-47T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71012531 | |||||||
| chr1:71012909 | C | A | 331 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.898-425G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71012909 | |||||||
| chr1:71012925 | ATAT | A | 329 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(326): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.898-444_898-442del others(3): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71012925 | |||||||
| chr1:71012958 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.898-474C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71012958 | |||||||
| chr1:71013301 | C | T | 8 | a0001c0001t0001g0143 a0001c0004t0002g0338 a0001c0004t0002g0339 others(5): Show |
8 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.898-817G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71013301 | |||||||
| chr1:71013443 | C | A | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.898-959G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71013443 | |||||||
| chr1:71013625 | C | T | 5 | a0001c0001t0001g0210 a0001c0001t0001g0221 a0001c0001t0001g0225 others(2): Show |
5 | HG00673.hp1 HG02523.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-1141G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71013625 | |||||||
| chr1:71013686 | G | T | 1 | a0001c0002t0010g0352 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.898-1202C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71013686 | |||||||
| chr1:71013702 | CA | C | 31 | a0001c0001t0001g0112 a0001c0001t0001g0133 a0001c0001t0001g0179 others(28): Show |
32 | HG00099.hp1 HG01069.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.898-1219delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71013702 | |||||||
| chr1:71013808 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0314 a0001c0001t0005g0107 |
3 | HG02572.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-1324C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71013808 | |||||||
| chr1:71014074 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.898-1590C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014074 | |||||||
| chr1:71014231 | A | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0033 others(3): Show |
6 | NA18949.hp1 NA18955.hp1 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-1747T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014231 | |||||||
| chr1:71014314 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.898-1830G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014314 | |||||||
| chr1:71014443 | C | A | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.898-1959G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014443 | |||||||
| chr1:71014598 | T | A | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.898-2114A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014598 | |||||||
| chr1:71014602 | C | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-2118G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014602 | |||||||
| chr1:71014878 | A | G | 1 | a0001c0009t0007g0337 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.898-2394T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014878 | |||||||
| chr1:71014893 | A | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-2409T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014893 | |||||||
| chr1:71014911 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.898-2427A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014911 | |||||||
| chr1:71014952 | C | T | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-2468G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014952 | |||||||
| chr1:71014966 | G | A | 332 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.898-2482C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014966 | |||||||
| chr1:71015115 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-2631T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015115 | |||||||
| chr1:71015161 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.898-2677A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015161 | |||||||
| chr1:71015256 | T | C | 128 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(125): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.898-2772A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015256 | |||||||
| chr1:71015320 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.898-2836C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015320 | |||||||
| chr1:71015321 | G | A | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-2837C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015321 | |||||||
| chr1:71015367 | A | G | 331 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.898-2883T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015367 | |||||||
| chr1:71015439 | G | A | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-2955C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015439 | |||||||
| chr1:71015484 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.898-3000A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015484 | |||||||
| chr1:71015863 | C | T | 1 | a0001c0009t0007g0337 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.898-3379G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015863 | |||||||
| chr1:71015968 | C | T | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.898-3484G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71015968 | |||||||
| chr1:71016053 | C | T | 1 | a0001c0002t0001g0016 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.898-3569G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016053 | |||||||
| chr1:71016060 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.898-3576C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016060 | |||||||
| chr1:71016349 | T | C | 5 | a0001c0001t0001g0205 a0001c0001t0001g0222 a0001c0001t0001g0232 others(2): Show |
5 | HG01123.hp1 HG01257.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-3865A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016349 | |||||||
| chr1:71016463 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.898-3979T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016463 | |||||||
| chr1:71016569 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.898-4085C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016569 | |||||||
| chr1:71016571 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.898-4087C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016571 | |||||||
| chr1:71016628 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.898-4144G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016628 | |||||||
| chr1:71016642 | A | C | 1 | a0001c0001t0002g0084 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.898-4158T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016642 | |||||||
| chr1:71016658 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.898-4174G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016658 | |||||||
| chr1:71016726 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.898-4242G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016726 | |||||||
| chr1:71016781 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.898-4297A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016781 | |||||||
| chr1:71016802 | C | CAA | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.898-4320_898-4319d others(4): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016802 | |||||||
| chr1:71016853 | A | C | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-4369T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016853 | |||||||
| chr1:71016922 | C | T | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-4438G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71016922 | |||||||
| chr1:71017003 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.898-4519G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017003 | |||||||
| chr1:71017061 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-4577G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017061 | |||||||
| chr1:71017061 | C | T | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.898-4577G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017061 | |||||||
| chr1:71017065 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-4581G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017065 | |||||||
| chr1:71017167 | C | T | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-4683G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017167 | |||||||
| chr1:71017190 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.898-4706A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017190 | |||||||
| chr1:71017474 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-4990T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017474 | |||||||
| chr1:71017486 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.898-5002A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017486 | |||||||
| chr1:71017681 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-5197T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017681 | |||||||
| chr1:71017878 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.898-5394G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017878 | |||||||
| chr1:71017944 | T | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-5460A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017944 | |||||||
| chr1:71017955 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.898-5471C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71017955 | |||||||
| chr1:71018040 | C | T | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-5556G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018040 | |||||||
| chr1:71018048 | A | T | 1 | a0002c0003t0001g0199 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.898-5564T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018048 | |||||||
| chr1:71018116 | A | T | 1 | a0001c0001t0003g0345 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.898-5632T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018116 | |||||||
| chr1:71018157 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.898-5673G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018157 | |||||||
| chr1:71018221 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-5737A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018221 | |||||||
| chr1:71018261 | AT | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.898-5778delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018261 | |||||||
| chr1:71018433 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.898-5949A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018433 | |||||||
| chr1:71018674 | T | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0083 others(12): Show |
16 | HG00673.hp2 HG02071.hp1 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.898-6190A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018674 | |||||||
| chr1:71018705 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.898-6221A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018705 | |||||||
| chr1:71018884 | G | A | 331 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.898-6400C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018884 | |||||||
| chr1:71018968 | C | A | 1 | a0001c0001t0002g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.898-6484G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018968 | |||||||
| chr1:71018998 | G | A | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.898-6514C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71018998 | |||||||
| chr1:71019353 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-6869G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019353 | |||||||
| chr1:71019375 | C | T | 1 | a0001c0002t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.898-6891G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019375 | |||||||
| chr1:71019376 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-6892C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019376 | |||||||
| chr1:71019475 | C | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-6991G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019475 | |||||||
| chr1:71019616 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-7132A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019616 | |||||||
| chr1:71019624 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.898-7140C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019624 | |||||||
| chr1:71019652 | T | C | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.898-7168A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019652 | |||||||
| chr1:71019731 | C | T | 102 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(99): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.898-7247G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019731 | |||||||
| chr1:71019834 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.898-7350C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019834 | |||||||
| chr1:71019941 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-7457C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019941 | |||||||
| chr1:71019972 | T | C | 324 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(321): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.898-7488A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71019972 | |||||||
| chr1:71020051 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0193 |
3 | HG03490.hp1 HG03492.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.898-7567T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020051 | |||||||
| chr1:71020150 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-7666C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020150 | |||||||
| chr1:71020195 | C | T | 1 | a0001c0002t0001g0322 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.898-7711G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020195 | |||||||
| chr1:71020264 | T | TA | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.898-7781dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020264 | |||||||
| chr1:71020286 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.898-7802C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020286 | |||||||
| chr1:71020287 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.898-7803G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020287 | |||||||
| chr1:71020294 | G | A | 5 | a0001c0001t0001g0205 a0001c0001t0001g0222 a0001c0001t0001g0232 others(2): Show |
5 | HG01123.hp1 HG01257.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-7810C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020294 | |||||||
| chr1:71020408 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.898-7924A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020408 | |||||||
| chr1:71020428 | T | C | 328 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(325): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.898-7944A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020428 | |||||||
| chr1:71020485 | T | C | 332 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.898-8001A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020485 | |||||||
| chr1:71020519 | G | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.898-8035C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020519 | |||||||
| chr1:71020663 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-8179T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020663 | |||||||
| chr1:71020697 | A | AGAGT | 4 | a0001c0001t0001g0077 a0001c0001t0001g0274 a0001c0001t0001g0276 others(1): Show |
4 | HG02257.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-8214_898-8213i others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | A | AGT | 85 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(82): Show |
89 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.898-8215_898-8214d others(4): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | A | AGTGT | 23 | a0001c0001t0001g0011 a0001c0001t0001g0065 a0001c0001t0001g0072 others(20): Show |
25 | HG00423.hp2 HG01074.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.898-8217_898-8214d others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | A | AGTGTGT | 6 | a0001c0001t0001g0071 a0001c0001t0001g0085 a0001c0001t0001g0206 others(3): Show |
6 | HG00639.hp2 HG02055.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-8219_898-8214d others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.898-8223_898-8214d others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | A | AGTGTGTG others(5): Show |
1 | a0003c0005t0002g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.898-8225_898-8214d others(14): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | A | AGTGTGTG others(9): Show |
1 | a0001c0001t0001g0260 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.898-8229_898-8214d others(18): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | A | AGTGTGTG others(25): Show |
1 | a0001c0001t0001g0214 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.898-8245_898-8214d others(34): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | AGT | A | 100 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(97): Show |
101 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.898-8215_898-8214d others(4): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020697 | AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0002g0032 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.898-8227_898-8214d others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020697 | |||||||
| chr1:71020699 | T | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
6 | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-8215A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020699 | |||||||
| chr1:71021019 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-8535A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021019 | |||||||
| chr1:71021089 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-8605G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021089 | |||||||
| chr1:71021126 | A | G | 70 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(67): Show |
71 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.898-8642T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021126 | |||||||
| chr1:71021182 | A | G | 2 | a0001c0002t0001g0323 a0001c0002t0001g0327 |
2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.898-8698T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021182 | |||||||
| chr1:71021298 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0260 |
2 | HG00280.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.898-8814A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021298 | |||||||
| chr1:71021344 | G | A | 5 | a0001c0002t0001g0328 a0001c0002t0001g0332 a0001c0002t0001g0333 others(2): Show |
5 | HG01074.hp1 HG02055.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-8860C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021344 | |||||||
| chr1:71021372 | A | G | 102 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(99): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.898-8888T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021372 | |||||||
| chr1:71021432 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-8948C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021432 | |||||||
| chr1:71021492 | GGGTGACA others(2591): Show |
G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-11606_898-9009 others(3): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021492 | |||||||
| chr1:71021562 | A | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0271 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.898-9078T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021562 | |||||||
| chr1:71021598 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.898-9114G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021598 | |||||||
| chr1:71021605 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.898-9121G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021605 | |||||||
| chr1:71021628 | A | G | 1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.898-9144T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021628 | |||||||
| chr1:71021679 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-9195A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021679 | |||||||
| chr1:71021702 | G | A | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(322): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.898-9218C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021702 | |||||||
| chr1:71021710 | C | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-9226G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021710 | |||||||
| chr1:71021711 | G | A | 1 | a0001c0002t0001g0323 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.898-9227C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021711 | |||||||
| chr1:71021724 | A | C | 102 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(99): Show |
103 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.898-9240T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021724 | |||||||
| chr1:71021802 | T | G | 1 | a0001c0001t0001g0237 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.898-9318A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021802 | |||||||
| chr1:71021808 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-9324C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021808 | |||||||
| chr1:71021853 | T | C | 1 | a0003c0005t0002g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.898-9369A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021853 | |||||||
| chr1:71022102 | G | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-9618C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022102 | |||||||
| chr1:71022107 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-9623G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022107 | |||||||
| chr1:71022129 | A | G | 110 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(107): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.898-9645T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022129 | |||||||
| chr1:71022323 | A | AAC | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-9840_898-9839i others(4): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022323 | |||||||
| chr1:71022326 | T | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-9842A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022326 | |||||||
| chr1:71022431 | A | T | 21 | a0001c0001t0001g0218 a0001c0002t0001g0016 a0001c0002t0001g0319 others(18): Show |
22 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-9947T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022431 | |||||||
| chr1:71022448 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.898-9964A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022448 | |||||||
| chr1:71022452 | A | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-9968T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022452 | |||||||
| chr1:71022518 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.898-10034T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022518 | |||||||
| chr1:71022604 | T | C | 1 | a0001c0001t0002g0026 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.898-10120A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022604 | |||||||
| chr1:71022606 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-10122G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022606 | |||||||
| chr1:71022607 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG01358.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-10123T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022607 | |||||||
| chr1:71022689 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.898-10205C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022689 | |||||||
| chr1:71022750 | T | TAC | 8 | a0001c0001t0001g0308 a0001c0001t0002g0288 a0001c0001t0002g0302 others(5): Show |
8 | HG01071.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-10268_898-1026 others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022750 | |||||||
| chr1:71022758 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.898-10274G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022758 | |||||||
| chr1:71022821 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.898-10337G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022821 | |||||||
| chr1:71022870 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.898-10386T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022870 | |||||||
| chr1:71022940 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.898-10456T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022940 | |||||||
| chr1:71022989 | C | A | 4 | a0001c0002t0001g0319 a0001c0002t0001g0320 a0001c0002t0001g0321 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-10505G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022989 | |||||||
| chr1:71022990 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.898-10506G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71022990 | |||||||
| chr1:71023044 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.898-10560A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023044 | |||||||
| chr1:71023063 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.898-10579A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023063 | |||||||
| chr1:71023151 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-10667C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023151 | |||||||
| chr1:71023186 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-10702T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023186 | |||||||
| chr1:71023246 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.898-10762A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023246 | |||||||
| chr1:71023307 | T | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
92 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.898-10823A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023307 | |||||||
| chr1:71023569 | C | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
196 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.898-11085G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023569 | |||||||
| chr1:71023596 | A | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.898-11112T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023596 | |||||||
| chr1:71023729 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.898-11245A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023729 | |||||||
| chr1:71023730 | C | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-11246G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023730 | |||||||
| chr1:71023755 | T | C | 105 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(102): Show |
110 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.898-11271A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023755 | |||||||
| chr1:71023813 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-11329G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023813 | |||||||
| chr1:71023893 | G | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0170 a0001c0001t0001g0187 others(5): Show |
8 | HG01109.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.898-11409C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023893 | |||||||
| chr1:71023948 | G | C | 1 | a0001c0002t0001g0325 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.898-11464C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023948 | |||||||
| chr1:71023961 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.898-11477G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023961 | |||||||
| chr1:71024120 | A | G | 1 | a0001c0001t0002g0311 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.898-11636T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024120 | |||||||
| chr1:71024163 | T | G | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(322): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.898-11679A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024163 | |||||||
| chr1:71024291 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-11807C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024291 | |||||||
| chr1:71024419 | G | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-11935C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024419 | |||||||
| chr1:71024439 | G | A | 190 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
196 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.898-11955C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024439 | |||||||
| chr1:71024458 | G | A | 20 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-11974C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024458 | |||||||
| chr1:71024459 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-11975C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024459 | |||||||
| chr1:71024513 | G | T | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.898-12029C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024513 | |||||||
| chr1:71024556 | A | C | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.898-12072T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024556 | |||||||
| chr1:71024645 | C | CT | 26 | a0001c0001t0001g0015 a0001c0001t0001g0096 a0001c0001t0001g0263 others(23): Show |
28 | HG00099.hp1 HG00438.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.898-12162dupA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024645 | |||||||
| chr1:71024645 | CT | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): Show |
94 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.898-12162delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024645 | |||||||
| chr1:71024645 | CTTTTTTT others(1): Show |
C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-12169_898-1216 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024645 | |||||||
| chr1:71024645 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG02083.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.898-12171_898-1216 others(14): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024645 | |||||||
| chr1:71024679 | C | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-12195G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024679 | |||||||
| chr1:71024710 | G | A | 52 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(49): Show |
53 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.898-12226C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024710 | |||||||
| chr1:71024744 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-12260C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024744 | |||||||
| chr1:71024780 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG01358.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-12296T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024780 | |||||||
| chr1:71024814 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0005g0107 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.898-12330G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024814 | |||||||
| chr1:71024816 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-12332C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024816 | |||||||
| chr1:71024817 | T | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-12333A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024817 | |||||||
| chr1:71024873 | TTTTA | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): Show |
28 | HG00323.hp1 HG01496.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.898-12393_898-1239 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024873 | |||||||
| chr1:71024873 | TTTTATTT others(1): Show |
T | 115 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(112): Show |
120 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.898-12397_898-1239 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024873 | |||||||
| chr1:71024873 | TTTTATTT others(5): Show |
T | 17 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(14): Show |
18 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.898-12401_898-1239 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024873 | |||||||
| chr1:71024873 | TTTTATTT others(9): Show |
T | 75 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(72): Show |
76 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.898-12405_898-1239 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024873 | |||||||
| chr1:71024873 | TTTTATTT others(13): Show |
T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-12409_898-1239 others(24): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024873 | |||||||
| chr1:71024952 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-12468G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024952 | |||||||
| chr1:71025093 | G | A | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.898-12609C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025093 | |||||||
| chr1:71025114 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0314 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-12630G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025114 | |||||||
| chr1:71025131 | C | CCCTT | 91 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
96 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.898-12651_898-1264 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025131 | |||||||
| chr1:71025131 | C | CCCTTCCT others(1): Show |
161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.898-12655_898-1264 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025131 | |||||||
| chr1:71025131 | C | CCCTTCCT others(5): Show |
35 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0106 others(32): Show |
35 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.898-12659_898-1264 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025131 | |||||||
| chr1:71025131 | C | CCCTTCCT others(9): Show |
27 | a0001c0001t0001g0085 a0001c0001t0001g0285 a0001c0001t0001g0286 others(24): Show |
27 | HG00639.hp2 HG01071.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.898-12663_898-1264 others(20): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025131 | |||||||
| chr1:71025131 | C | CCCTTCCT others(13): Show |
7 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(4): Show |
7 | HG01891.hp2 HG02723.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.898-12667_898-1264 others(24): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025131 | |||||||
| chr1:71025131 | C | CCCTTCCT others(17): Show |
1 | a0001c0001t0005g0107 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.898-12671_898-1264 others(28): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025131 | |||||||
| chr1:71025131 | C | CCCTTCCT others(25): Show |
1 | a0001c0001t0001g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.898-12679_898-1264 others(36): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025131 | |||||||
| chr1:71025165 | T | C | 26 | a0001c0001t0001g0308 a0001c0001t0002g0158 a0001c0001t0002g0159 others(23): Show |
26 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.898-12681A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025165 | |||||||
| chr1:71025171 | T | A | 20 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-12687A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025171 | |||||||
| chr1:71025173 | C | CTTCCTTC others(10): Show |
1 | a0001c0001t0002g0302 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.898-12690_898-1268 others(21): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025173 | |||||||
| chr1:71025181 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.898-12697G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025181 | |||||||
| chr1:71025293 | G | A | 20 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-12809C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025293 | |||||||
| chr1:71025396 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.898-12912C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025396 | |||||||
| chr1:71025497 | T | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-13013A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025497 | |||||||
| chr1:71025527 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.898-13043C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025527 | |||||||
| chr1:71025540 | TGTAA | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-13060_898-1305 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025540 | |||||||
| chr1:71025572 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.898-13088C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025572 | |||||||
| chr1:71025589 | C | A | 18 | a0001c0001t0001g0308 a0001c0001t0002g0158 a0001c0001t0002g0159 others(15): Show |
18 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.898-13105G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025589 | |||||||
| chr1:71025646 | A | G | 4 | a0001c0002t0001g0319 a0001c0002t0001g0320 a0001c0002t0001g0321 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-13162T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025646 | |||||||
| chr1:71025674 | A | G | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.898-13190T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025674 | |||||||
| chr1:71025690 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-13206C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025690 | |||||||
| chr1:71025774 | T | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-13290A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025774 | |||||||
| chr1:71025806 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-13322C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025806 | |||||||
| chr1:71025923 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-13439C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71025923 | |||||||
| chr1:71026028 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-13544G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026028 | |||||||
| chr1:71026032 | G | A | 75 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(72): Show |
76 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.898-13548C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026032 | |||||||
| chr1:71026087 | C | T | 1 | a0001c0001t0001g0006 | 2 | NA18988.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.898-13603G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026087 | |||||||
| chr1:71026092 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.898-13608C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026092 | |||||||
| chr1:71026207 | A | T | 124 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(121): Show |
129 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.898-13723T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026207 | |||||||
| chr1:71026242 | T | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-13758A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026242 | |||||||
| chr1:71026256 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0192 |
2 | HG01175.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.898-13772G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026256 | |||||||
| chr1:71026344 | T | C | 20 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.898-13860A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026344 | |||||||
| chr1:71026384 | T | A | 6 | a0001c0001t0001g0308 a0001c0001t0002g0288 a0001c0001t0002g0307 others(3): Show |
6 | HG01071.hp2 HG01496.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-13900A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026384 | |||||||
| chr1:71026390 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.898-13906A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026390 | |||||||
| chr1:71026408 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0004g0280 a0001c0001t0005g0107 |
3 | HG02257.hp2 HG02572.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.898-13924C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026408 | |||||||
| chr1:71026450 | G | A | 1 | a0001c0001t0002g0273 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.898-13966C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026450 | |||||||
| chr1:71026452 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-13968T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026452 | |||||||
| chr1:71026749 | T | G | 1 | a0001c0001t0002g0050 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.898-14265A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026749 | |||||||
| chr1:71026900 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.898-14416C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026900 | |||||||
| chr1:71026910 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0005g0107 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.898-14426A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026910 | |||||||
| chr1:71027017 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.898-14533G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027017 | |||||||
| chr1:71027020 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.898-14536C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027020 | |||||||
| chr1:71027042 | T | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-14558A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027042 | |||||||
| chr1:71027156 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-14672A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027156 | |||||||
| chr1:71027205 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-14721G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027205 | |||||||
| chr1:71027206 | GAGGCTGG others(8): Show |
G | 57 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(54): Show |
58 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.898-14737_898-1472 others(19): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027206 | |||||||
| chr1:71027209 | G | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-14725C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027209 | |||||||
| chr1:71027314 | C | T | 75 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(72): Show |
76 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.898-14830G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027314 | |||||||
| chr1:71027345 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.898-14861T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027345 | |||||||
| chr1:71027519 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-15035A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027519 | |||||||
| chr1:71027520 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0005g0275 |
2 | HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.898-15036T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027520 | |||||||
| chr1:71027549 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-15065T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027549 | |||||||
| chr1:71027610 | T | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-15126A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027610 | |||||||
| chr1:71027617 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0004g0280 a0001c0001t0005g0107 |
3 | HG02257.hp2 HG02572.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.898-15133C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027617 | |||||||
| chr1:71027736 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.898-15252T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027736 | |||||||
| chr1:71027739 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.898-15255T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027739 | |||||||
| chr1:71027956 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(114): Show |
122 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.898-15472A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027956 | |||||||
| chr1:71028009 | T | C | 330 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(327): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.898-15525A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028009 | |||||||
| chr1:71028140 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.898-15656G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028140 | |||||||
| chr1:71028154 | C | A | 11 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(8): Show |
12 | HG00099.hp1 HG01255.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.898-15670G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028154 | |||||||
| chr1:71028221 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.898-15737A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028221 | |||||||
| chr1:71028436 | T | G | 2 | a0001c0001t0001g0106 a0001c0001t0004g0075 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.898-15952A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028436 | |||||||
| chr1:71028494 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.898-16010T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028494 | |||||||
| chr1:71028584 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
5 | HG02132.hp1 NA18950.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-16100C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028584 | |||||||
| chr1:71028612 | T | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.898-16128A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028612 | |||||||
| chr1:71028664 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.898-16180G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028664 | |||||||
| chr1:71028682 | A | G | 106 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.898-16198T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028682 | |||||||
| chr1:71028785 | G | T | 1 | a0001c0001t0002g0301 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.898-16301C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028785 | |||||||
| chr1:71028834 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.898-16350C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028834 | |||||||
| chr1:71028841 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG00323.hp1 HG01106.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-16357T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71028841 | |||||||
| chr1:71029016 | T | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
8 | HG02056.hp1 NA18959.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.898-16532A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029016 | |||||||
| chr1:71029139 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.898-16655C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029139 | |||||||
| chr1:71029451 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.898-16967G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029451 | |||||||
| chr1:71029535 | T | C | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.898-17051A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029535 | |||||||
| chr1:71029586 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.897+17095A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029586 | |||||||
| chr1:71029666 | C | T | 68 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(65): Show |
69 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.897+17015G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029666 | |||||||
| chr1:71029686 | C | G | 328 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(325): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.897+16995G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029686 | |||||||
| chr1:71029752 | C | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.897+16929G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029752 | |||||||
| chr1:71029820 | G | A | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
7 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+16861C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029820 | |||||||
| chr1:71029874 | C | A | 1 | a0001c0001t0002g0315 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.897+16807G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029874 | |||||||
| chr1:71029882 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+16799G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029882 | |||||||
| chr1:71029883 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+16798C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029883 | |||||||
| chr1:71029906 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.897+16775T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029906 | |||||||
| chr1:71029907 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.897+16774G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029907 | |||||||
| chr1:71029907 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.897+16774G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029907 | |||||||
| chr1:71029926 | A | AAAT | 81 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0013 others(78): Show |
85 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.897+16752_897+1675 others(7): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029926 | |||||||
| chr1:71029926 | A | AAATAAT | 9 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0001g0203 others(6): Show |
10 | HG01515.hp2 HG02922.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.897+16749_897+1675 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029926 | |||||||
| chr1:71029926 | A | AAATAATA others(2): Show |
14 | a0001c0001t0001g0196 a0001c0001t0001g0270 a0001c0001t0001g0284 others(11): Show |
14 | HG01255.hp1 HG02080.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.897+16746_897+1675 others(13): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029926 | |||||||
| chr1:71029926 | A | AAATAATA others(5): Show |
5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.897+16743_897+1675 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029926 | |||||||
| chr1:71029926 | AAAT | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0077 others(32): Show |
37 | HG00408.hp2 HG00642.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.897+16752_897+1675 others(7): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029926 | |||||||
| chr1:71029926 | AAATAAT | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.897+16749_897+1675 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029926 | |||||||
| chr1:71029926 | AAATAATA others(2): Show |
A | 13 | a0001c0001t0001g0308 a0001c0001t0002g0288 a0001c0001t0002g0301 others(10): Show |
13 | HG01071.hp2 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.897+16746_897+1675 others(13): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029926 | |||||||
| chr1:71029955 | A | T | 1 | a0001c0002t0001g0016 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.897+16726T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029955 | |||||||
| chr1:71029962 | C | T | 56 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.897+16719G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029962 | |||||||
| chr1:71029963 | A | AAT | 33 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0063 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.897+16717_897+1671 others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029963 | |||||||
| chr1:71029964 | A | AT | 10 | a0001c0001t0001g0029 a0001c0001t0002g0003 a0001c0001t0002g0028 others(7): Show |
11 | HG00544.hp1 HG01256.hp1 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.897+16716_897+1671 others(5): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029964 | |||||||
| chr1:71029965 | A | C | 11 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0194 others(8): Show |
11 | HG00280.hp2 HG00741.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.897+16716T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029965 | |||||||
| chr1:71029966 | A | C | 33 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0063 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.897+16715T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029966 | |||||||
| chr1:71029966 | AT | A | 11 | a0001c0001t0002g0104 a0001c0001t0002g0105 a0001c0001t0002g0194 others(8): Show |
11 | HG00280.hp2 HG00741.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.897+16714delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029966 | |||||||
| chr1:71029967 | T | A | 33 | a0001c0001t0001g0024 a0001c0001t0001g0038 a0001c0001t0001g0063 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.897+16714A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029967 | |||||||
| chr1:71029967 | T | TAACA | 12 | a0001c0001t0001g0029 a0001c0001t0002g0003 a0001c0001t0002g0028 others(9): Show |
13 | HG00544.hp1 HG01256.hp1 HG04204.hp1 others(10): Show |
intron_variant | MODIFIER | c.897+16713_897+1671 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029967 | |||||||
| chr1:71029970 | G | A | 56 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.897+16711C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029970 | |||||||
| chr1:71029970 | GTAAA | G | 12 | a0001c0001t0001g0053 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
12 | HG01255.hp1 HG01891.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.897+16707_897+1671 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029970 | |||||||
| chr1:71029974 | A | G | 56 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(53): Show |
57 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.897+16707T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71029974 | |||||||
| chr1:71030166 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+16515T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030166 | |||||||
| chr1:71030453 | T | C | 332 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.897+16228A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030453 | |||||||
| chr1:71030475 | T | C | 1 | a0001c0001t0004g0280 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.897+16206A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030475 | |||||||
| chr1:71030531 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.897+16150C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030531 | |||||||
| chr1:71030642 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0005g0107 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.897+16039C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030642 | |||||||
| chr1:71030648 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+16033C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030648 | |||||||
| chr1:71030670 | A | G | 68 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(65): Show |
69 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.897+16011T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030670 | |||||||
| chr1:71030809 | A | T | 1 | a0001c0001t0002g0027 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.897+15872T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030809 | |||||||
| chr1:71030836 | A | AT | 122 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(119): Show |
127 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.897+15844dupA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030836 | |||||||
| chr1:71031245 | AAC | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(27): Show |
37 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.897+15434_897+1543 others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031245 | |||||||
| chr1:71031245 | AACAC | A | 88 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(85): Show |
89 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.897+15432_897+1543 others(8): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031245 | |||||||
| chr1:71031245 | AACACAC | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.897+15430_897+1543 others(10): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031245 | |||||||
| chr1:71031245 | AACACACA others(1): Show |
A | 35 | a0001c0001t0001g0085 a0001c0001t0001g0151 a0001c0001t0001g0186 others(32): Show |
35 | HG00621.hp1 HG01071.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.897+15428_897+1543 others(12): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031245 | |||||||
| chr1:71031245 | AACACACA others(3): Show |
A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(92): Show |
100 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.897+15426_897+1543 others(14): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031245 | |||||||
| chr1:71031245 | AACACACA others(7): Show |
A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG00408.hp2 NA18985.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.897+15422_897+1543 others(18): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031245 | |||||||
| chr1:71031376 | A | C | 1 | a0001c0001t0003g0345 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.897+15305T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031376 | |||||||
| chr1:71031412 | T | C | 1 | a0001c0002t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.897+15269A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031412 | |||||||
| chr1:71031516 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.897+15165A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031516 | |||||||
| chr1:71031571 | C | A | 9 | a0001c0002t0001g0328 a0001c0002t0001g0329 a0001c0002t0001g0330 others(6): Show |
9 | HG01074.hp1 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+15110G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031571 | |||||||
| chr1:71031898 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+14783C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71031898 | |||||||
| chr1:71032190 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+14491C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032190 | |||||||
| chr1:71032400 | TCTATGAT others(5): Show |
T | 1 | a0001c0001t0001g0120 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.897+14269_897+1428 others(16): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032400 | |||||||
| chr1:71032558 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0192 |
2 | HG01175.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.897+14123G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032558 | |||||||
| chr1:71032563 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+14118C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032563 | |||||||
| chr1:71032679 | C | T | 91 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(88): Show |
96 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.897+14002G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032679 | |||||||
| chr1:71032878 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.897+13803C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032878 | |||||||
| chr1:71032930 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.897+13751T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032930 | |||||||
| chr1:71032941 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.897+13740G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71032941 | |||||||
| chr1:71033078 | C | T | 7 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(4): Show |
7 | HG01255.hp1 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.897+13603G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71033078 | |||||||
| chr1:71033380 | C | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0279 a0001c0001t0001g0316 |
4 | HG02109.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+13301G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71033380 | |||||||
| chr1:71033475 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.897+13206G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71033475 | |||||||
| chr1:71033603 | A | G | 68 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(65): Show |
69 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.897+13078T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71033603 | |||||||
| chr1:71033904 | A | G | 4 | a0001c0002t0001g0319 a0001c0002t0001g0320 a0001c0002t0001g0321 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+12777T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71033904 | |||||||
| chr1:71033918 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.897+12763G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71033918 | |||||||
| chr1:71033987 | TCTTTAAA others(12): Show |
T | 1 | a0001c0002t0001g0332 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.897+12675_897+1269 others(23): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71033987 | |||||||
| chr1:71034160 | T | C | 3 | a0001c0001t0001g0170 a0001c0001t0001g0187 a0001c0001t0001g0291 |
3 | HG01109.hp2 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.897+12521A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034160 | |||||||
| chr1:71034188 | T | TATC | 347 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.897+12492_897+1249 others(7): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034188 | |||||||
| chr1:71034218 | A | G | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+12463T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034218 | |||||||
| chr1:71034278 | G | A | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.897+12403C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034278 | |||||||
| chr1:71034416 | A | G | 92 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(89): Show |
94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.897+12265T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034416 | |||||||
| chr1:71034486 | G | A | 1 | a0001c0001t0001g0009 | 2 | NA18968.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.897+12195C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034486 | |||||||
| chr1:71034505 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.897+12176A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034505 | |||||||
| chr1:71034828 | A | G | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
7 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+11853T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034828 | |||||||
| chr1:71034913 | T | A | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.897+11768A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034913 | |||||||
| chr1:71034937 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.897+11744C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71034937 | |||||||
| chr1:71035020 | CT | C | 68 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0038 others(65): Show |
69 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.897+11660delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71035020 | |||||||
| chr1:71035057 | T | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0057 others(25): Show |
29 | HG00438.hp2 HG01255.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.897+11624A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71035057 | |||||||
| chr1:71035343 | G | T | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.897+11338C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71035343 | |||||||
| chr1:71035592 | C | G | 1 | a0001c0001t0002g0287 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.897+11089G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71035592 | |||||||
| chr1:71035779 | T | G | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+10902A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71035779 | |||||||
| chr1:71035791 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0262 |
2 | NA18989.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.897+10890T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71035791 | |||||||
| chr1:71036173 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG02083.hp1 HG02135.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+10508T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036173 | |||||||
| chr1:71036296 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0005g0107 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.897+10385C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036296 | |||||||
| chr1:71036382 | G | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(122): Show |
130 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.897+10299C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036382 | |||||||
| chr1:71036407 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.897+10274T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036407 | |||||||
| chr1:71036475 | C | G | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.897+10206G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036475 | |||||||
| chr1:71036563 | C | A | 330 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(327): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.897+10118G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036563 | |||||||
| chr1:71036567 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.897+10114T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036567 | |||||||
| chr1:71036597 | T | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.897+10084A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036597 | |||||||
| chr1:71036616 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.897+10065C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036616 | |||||||
| chr1:71036633 | G | T | 1 | a0001c0002t0001g0329 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.897+10048C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036633 | |||||||
| chr1:71036637 | G | A | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+10044C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036637 | |||||||
| chr1:71036707 | T | C | 4 | a0001c0002t0001g0323 a0001c0002t0001g0327 a0003c0005t0002g0289 others(1): Show |
4 | HG00639.hp2 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+9974A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036707 | |||||||
| chr1:71036712 | T | G | 4 | a0001c0002t0001g0323 a0001c0002t0001g0327 a0003c0005t0002g0289 others(1): Show |
4 | HG00639.hp2 HG03195.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+9969A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036712 | |||||||
| chr1:71036770 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.897+9911G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036770 | |||||||
| chr1:71036787 | C | T | 1 | a0001c0001t0003g0351 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.897+9894G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036787 | |||||||
| chr1:71036824 | A | G | 347 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.897+9857T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036824 | |||||||
| chr1:71036838 | C | CA | 100 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.897+9842dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036838 | |||||||
| chr1:71036998 | C | CT | 311 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(308): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.897+9682_897+9683i others(3): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036998 | |||||||
| chr1:71036999 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+9682C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036999 | |||||||
| chr1:71037173 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.897+9508T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037173 | |||||||
| chr1:71037189 | C | T | 23 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0005g0275 others(20): Show |
24 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.897+9492G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037189 | |||||||
| chr1:71037203 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+9478G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037203 | |||||||
| chr1:71037229 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.897+9452G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037229 | |||||||
| chr1:71037350 | A | C | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+9331T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037350 | |||||||
| chr1:71037422 | T | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.897+9259A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037422 | |||||||
| chr1:71037427 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.897+9254C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037427 | |||||||
| chr1:71037454 | T | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+9227A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037454 | |||||||
| chr1:71037518 | G | A | 221 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(218): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.897+9163C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037518 | |||||||
| chr1:71037634 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+9047G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037634 | |||||||
| chr1:71037672 | A | G | 4 | a0001c0002t0001g0329 a0001c0002t0001g0330 a0001c0002t0001g0331 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+9009T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037672 | |||||||
| chr1:71037764 | G | A | 220 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(217): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.897+8917C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71037764 | |||||||
| chr1:71038004 | G | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.897+8677C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038004 | |||||||
| chr1:71038147 | T | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+8534A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038147 | |||||||
| chr1:71038257 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+8424C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038257 | |||||||
| chr1:71038319 | A | G | 23 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0005g0275 others(20): Show |
24 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.897+8362T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038319 | |||||||
| chr1:71038441 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.897+8240A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038441 | |||||||
| chr1:71038538 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+8143G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038538 | |||||||
| chr1:71038574 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.897+8107T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038574 | |||||||
| chr1:71038631 | C | T | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+8050G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038631 | |||||||
| chr1:71038692 | T | G | 2 | a0001c0001t0001g0077 a0001c0001t0005g0107 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.897+7989A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038692 | |||||||
| chr1:71038707 | A | G | 324 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(321): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.897+7974T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038707 | |||||||
| chr1:71038820 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.897+7861G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038820 | |||||||
| chr1:71038855 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.897+7826T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038855 | |||||||
| chr1:71038994 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.897+7687G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038994 | |||||||
| chr1:71038995 | A | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(117): Show |
125 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.897+7686T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71038995 | |||||||
| chr1:71039035 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+7646G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039035 | |||||||
| chr1:71039067 | C | G | 1 | a0001c0001t0001g0024 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.897+7614G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039067 | |||||||
| chr1:71039130 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
5 | HG02132.hp1 NA18950.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.897+7551T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039130 | |||||||
| chr1:71039150 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.897+7531C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039150 | |||||||
| chr1:71039152 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.897+7529G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039152 | |||||||
| chr1:71039156 | C | T | 2 | a0003c0005t0002g0289 a0003c0005t0002g0290 |
2 | HG00639.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.897+7525G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039156 | |||||||
| chr1:71039507 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.897+7174C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039507 | |||||||
| chr1:71039510 | T | C | 1 | a0001c0002t0006g0326 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.897+7171A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039510 | |||||||
| chr1:71039518 | T | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0269 a0001c0001t0004g0280 others(2): Show |
5 | HG02897.hp1 HG03942.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.897+7163A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039518 | |||||||
| chr1:71039522 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.897+7159G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039522 | |||||||
| chr1:71039597 | C | T | 2 | a0001c0002t0001g0323 a0001c0002t0001g0327 |
2 | HG03195.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.897+7084G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039597 | |||||||
| chr1:71039649 | C | CA | 49 | a0001c0001t0001g0015 a0001c0001t0001g0085 a0001c0001t0001g0160 others(46): Show |
50 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.897+7031dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039649 | |||||||
| chr1:71039649 | CAAAAAAA | C | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+7025_897+7031d others(9): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039649 | |||||||
| chr1:71039663 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.897+7018T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039663 | |||||||
| chr1:71039664 | A | AG | 147 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(144): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.897+7016_897+7017i others(3): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039664 | |||||||
| chr1:71039664 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG01358.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+7017T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039664 | |||||||
| chr1:71039769 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0004g0280 |
2 | HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.897+6912T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039769 | |||||||
| chr1:71039916 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0080 |
2 | NA18940.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.897+6765T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039916 | |||||||
| chr1:71040081 | GAAGA | G | 6 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(3): Show |
6 | HG01192.hp2 HG01884.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.897+6596_897+6599d others(6): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040081 | |||||||
| chr1:71040146 | A | G | 20 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.897+6535T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040146 | |||||||
| chr1:71040222 | A | G | 6 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
6 | HG02922.hp1 HG02976.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.897+6459T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040222 | |||||||
| chr1:71040325 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+6356G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040325 | |||||||
| chr1:71040326 | G | A | 9 | a0001c0002t0001g0328 a0001c0002t0001g0329 a0001c0002t0001g0330 others(6): Show |
9 | HG01074.hp1 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+6355C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040326 | |||||||
| chr1:71040381 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.897+6300G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040381 | |||||||
| chr1:71040439 | T | TA | 9 | a0001c0001t0001g0245 a0001c0001t0001g0281 a0001c0001t0001g0282 others(6): Show |
9 | HG01255.hp1 HG01891.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+6241dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040439 | |||||||
| chr1:71040466 | G | C | 4 | a0001c0001t0001g0087 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG01943.hp1 HG02148.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+6215C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040466 | |||||||
| chr1:71040664 | C | T | 46 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0276 others(43): Show |
47 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.897+6017G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040664 | |||||||
| chr1:71040668 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.897+6013G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040668 | |||||||
| chr1:71040883 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.897+5798C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040883 | |||||||
| chr1:71040886 | A | C | 1 | a0001c0001t0001g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.897+5795T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040886 | |||||||
| chr1:71040899 | C | T | 84 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(81): Show |
88 | HG00140.hp2 HG00323.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.897+5782G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71040899 | |||||||
| chr1:71041110 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+5571G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041110 | |||||||
| chr1:71041161 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.897+5520C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041161 | |||||||
| chr1:71041177 | G | A | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+5504C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041177 | |||||||
| chr1:71041178 | T | A | 1 | a0001c0001t0002g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.897+5503A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041178 | |||||||
| chr1:71041552 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.897+5129G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041552 | |||||||
| chr1:71041620 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.897+5061C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041620 | |||||||
| chr1:71041625 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897+5056T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041625 | |||||||
| chr1:71041711 | GA | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG01167.hp2 HG01169.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.897+4969delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041711 | |||||||
| chr1:71041725 | G | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0246 |
2 | HG01257.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.897+4956C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041725 | |||||||
| chr1:71041765 | T | G | 1 | a0001c0002t0001g0016 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.897+4916A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041765 | |||||||
| chr1:71041805 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.897+4876G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041805 | |||||||
| chr1:71041858 | G | T | 347 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(344): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.897+4823C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041858 | |||||||
| chr1:71041902 | C | T | 1 | a0001c0001t0002g0023 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.897+4779G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71041902 | |||||||
| chr1:71042121 | G | C | 1 | a0001c0001t0002g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.897+4560C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71042121 | |||||||
| chr1:71042176 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897+4505G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71042176 | |||||||
| chr1:71042426 | T | G | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.897+4255A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71042426 | |||||||
| chr1:71042519 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897+4162T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71042519 | |||||||
| chr1:71042867 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.897+3814C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71042867 | |||||||
| chr1:71042919 | T | C | 8 | a0001c0001t0001g0200 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG00621.hp1 HG02155.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.897+3762A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71042919 | |||||||
| chr1:71043273 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0171 |
2 | HG01943.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.897+3408G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043273 | |||||||
| chr1:71043279 | G | A | 332 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.897+3402C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043279 | |||||||
| chr1:71043370 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+3311C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043370 | |||||||
| chr1:71043418 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.897+3263A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043418 | |||||||
| chr1:71043424 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(246): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.897+3257C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043424 | |||||||
| chr1:71043623 | T | G | 1 | a0001c0002t0001g0016 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.897+3058A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043623 | |||||||
| chr1:71043648 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.897+3033C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043648 | |||||||
| chr1:71043652 | A | T | 20 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.897+3029T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043652 | |||||||
| chr1:71043792 | T | C | 1 | a0001c0002t0001g0322 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.897+2889A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043792 | |||||||
| chr1:71043807 | G | GT | 8 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0002g0108 others(5): Show |
9 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.897+2873dupA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043807 | |||||||
| chr1:71043807 | GT | G | 8 | a0001c0001t0001g0200 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG00621.hp1 HG02155.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.897+2873delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043807 | |||||||
| chr1:71043809 | T | A | 8 | a0001c0001t0001g0200 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
8 | HG00621.hp1 HG02155.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.897+2872A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043809 | |||||||
| chr1:71043917 | A | G | 37 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(34): Show |
37 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.897+2764T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043917 | |||||||
| chr1:71043933 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+2748G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71043933 | |||||||
| chr1:71044017 | A | G | 20 | a0001c0002t0001g0016 a0001c0002t0001g0319 a0001c0002t0001g0320 others(17): Show |
21 | HG00099.hp1 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.897+2664T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044017 | |||||||
| chr1:71044051 | A | G | 4 | a0001c0002t0001g0319 a0001c0002t0001g0320 a0001c0002t0001g0321 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+2630T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044051 | |||||||
| chr1:71044096 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.897+2585C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044096 | |||||||
| chr1:71044229 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.897+2452C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044229 | |||||||
| chr1:71044235 | G | C | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+2446C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044235 | |||||||
| chr1:71044310 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897+2371C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044310 | |||||||
| chr1:71044439 | C | CA | 32 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0164 others(29): Show |
32 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.897+2241dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044439 | |||||||
| chr1:71044439 | CA | C | 8 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(5): Show |
8 | HG01257.hp1 HG01515.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.897+2241delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044439 | |||||||
| chr1:71044481 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897+2200A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044481 | |||||||
| chr1:71044518 | T | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | NA19009.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.897+2163A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044518 | |||||||
| chr1:71044602 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.897+2079G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044602 | |||||||
| chr1:71044675 | G | GC | 3 | a0001c0001t0001g0013 a0001c0001t0001g0257 a0001c0001t0001g0258 |
4 | HG01358.hp1 HG01934.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.897+2005dupG | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044675 | |||||||
| chr1:71044736 | G | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(283): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.897+1945C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044736 | |||||||
| chr1:71044829 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.897+1852A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044829 | |||||||
| chr1:71044988 | C | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0276 others(6): Show |
10 | HG02109.hp1 HG02922.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.897+1693G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044988 | |||||||
| chr1:71045029 | G | C | 1 | a0001c0001t0002g0079 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.897+1652C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71045029 | |||||||
| chr1:71045677 | T | G | 7 | a0001c0004t0002g0338 a0001c0004t0002g0339 a0001c0004t0002g0340 others(4): Show |
7 | HG02145.hp1 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+1004A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71045677 | |||||||
| chr1:71045832 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.897+849C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71045832 | |||||||
| chr1:71045835 | A | G | 332 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.897+846T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71045835 | |||||||
| chr1:71045883 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.897+798A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71045883 | |||||||
| chr1:71045905 | G | T | 1 | a0001c0004t0002g0338 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.897+776C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71045905 | |||||||
| chr1:71045915 | C | G | 332 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.897+766G>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71045915 | |||||||
| chr1:71046123 | T | TA | 7 | a0001c0001t0001g0106 a0001c0001t0001g0272 a0001c0001t0002g0104 others(4): Show |
7 | HG01891.hp1 HG02809.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.897+557dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046123 | |||||||
| chr1:71046123 | TA | T | 7 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(4): Show |
7 | HG01192.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.897+557delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046123 | |||||||
| chr1:71046124 | A | T | 3 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0273 |
3 | HG02083.hp2 NA18948.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.897+557T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046124 | |||||||
| chr1:71046128 | A | T | 45 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0276 others(42): Show |
46 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.897+553T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046128 | |||||||
| chr1:71046232 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.897+449C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046232 | |||||||
| chr1:71046285 | C | CA | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.897+395dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046285 | |||||||
| chr1:71046285 | C | CAA | 48 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0167 others(45): Show |
50 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.897+394_897+395dup others(2): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046285 | |||||||
| chr1:71046285 | C | CAAA | 6 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0002g0194 others(3): Show |
6 | HG02970.hp1 HG03098.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.897+393_897+395dup others(3): Show |
PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046285 | |||||||
| chr1:71046285 | CA | C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0025 others(54): Show |
59 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.897+395delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046285 | |||||||
| chr1:71046306 | A | C | 49 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(46): Show |
50 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.897+375T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046306 | |||||||
| chr1:71046307 | C | A | 95 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.897+374G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046307 | |||||||
| chr1:71046333 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.897+348T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046333 | |||||||
| chr1:71046477 | T | C | 45 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0276 others(42): Show |
46 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.897+204A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046477 | |||||||
| chr1:71046495 | G | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG00323.hp1 HG01106.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+186C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046495 |