| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 390 | 360 | 81 | 61 | 164 | 14 | 38 | 128 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0002 | 0/0 | 390 | 7 | 0 | 2 | 5 | 0 | 0 | 5 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0003 | 0/0 | 390 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0004 | 0/0 | 390 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0005 | 0/0 | 225 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0006 | 0/0 | 390 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1173 | 331 | 58 | 56 | 164 | 13 | 38 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0002 | 0/0 | 1173 | 21 | 16 | 4 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0003 | 0/0 | 1173 | 7 | 0 | 2 | 5 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0004 | 0/0 | 1173 | 6 | 6 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0005 | 0/0 | 1173 | 2 | 1 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0006 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0007 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0008 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0009 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| c0010 | 0/0 | 1124 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1188 | 265 | 49 | 48 | 126 | 11 | 30 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0002 | 0/1 | 1188 | 91 | 28 | 13 | 43 | 1 | 5 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0003 | 0/0 | 1188 | 7 | 0 | 3 | 0 | 1 | 3 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0004 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0005 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0006 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0007 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0008 | 0/0 | 1188 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0009 | 0/0 | 1188 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| t0010 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0319 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1173 | 331 | 58 | 56 | 164 | 13 | 38 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0002 | 0/0 | 1173 | 21 | 16 | 4 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0004 | 0/0 | 1173 | 6 | 6 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0007 | 0/0 | 1173 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0009 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0002c0003 | 0/0 | 1173 | 7 | 0 | 2 | 5 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0003c0005 | 0/0 | 1173 | 2 | 1 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0004c0008 | 0/0 | 1173 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0005c0010 | 0/0 | 1124 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0006c0006 | 0/0 | 1173 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2360 | 237 | 34 | 41 | 121 | 10 | 30 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0001t0002 | 0/1 | 2360 | 81 | 20 | 12 | 42 | 1 | 5 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0001t0003 | 0/0 | 2360 | 7 | 0 | 3 | 0 | 1 | 3 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0001t0004 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0001t0005 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0001t0008 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0001t0009 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0002t0001 | 0/0 | 2360 | 19 | 14 | 4 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0002t0006 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0002t0010 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0004t0002 | 0/0 | 2360 | 6 | 6 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0007t0001 | 0/0 | 2360 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0001c0009t0007 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0002c0003t0001 | 0/0 | 2360 | 7 | 0 | 2 | 5 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0003c0005t0002 | 0/0 | 2360 | 2 | 1 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0004c0008t0002 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0005c0010t0002 | 0/0 | 2311 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| a0006c0006t0001 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | copy fasta | chr1 | 70965782 | 71052816 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 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 | 2 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0051 | 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 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0062 | 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 |
| a0001c0001t0001g0067 | 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 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0199 | 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 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0242 | 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 | 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 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 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 | 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 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0267 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| 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 | 1 | 0 | 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 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0290 | 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 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0025 | 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 |
| a0001c0001t0002g0029 | 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 |
| 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 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0038 | 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 |
| a0001c0001t0002g0043 | 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 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 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 | 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 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0319 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0006g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0002t0010g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0004t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0007t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0001c0009t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0003c0005t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0003c0005t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0004c0008t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0005c0010t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| a0006c0006t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0333 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0356 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | FIN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00609 | hp1 | a0001 | c0001 | t0009 | g0060 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00639 | hp2 | a0003 | c0005 | t0002 | g0297 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0274 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0357 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0244 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0337 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0355 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0334 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | IBS | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01884 | hp1 | a0001 | c0009 | t0007 | g0346 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0360 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02004 | hp1 | a0001 | c0007 | t0001 | g0181 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0341 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0272 | 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 | a0005 | c0010 | t0002 | g0353 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0339 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0301 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0303 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0342 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0331 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0328 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0359 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0348 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0343 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02922 | hp2 | a0001 | c0002 | t0010 | g0361 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0329 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0340 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0351 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0307 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0344 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0302 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0299 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0332 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03209 | hp1 | a0001 | c0004 | t0002 | g0350 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03516 | hp2 | a0006 | c0006 | t0001 | g0011 | AFR | ESN | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03540 | hp1 | a0001 | c0004 | t0002 | g0349 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0322 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0345 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0358 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0354 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0338 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18906 | hp1 | a0001 | c0004 | t0002 | g0352 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18946 | hp2 | a0002 | c0003 | t0001 | g0232 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18956 | hp2 | a0004 | c0008 | t0002 | g0036 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0201 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0202 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19043 | hp1 | a0001 | c0002 | t0006 | g0335 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0233 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ASW | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ASW | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0318 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20805 | hp2 | a0001 | c0001 | t0008 | g0142 | EUR | TSI | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0347 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG06807 | hp1 | a0003 | c0005 | t0002 | g0296 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0336 | AFR | USA | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | LWK | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0319 | REF | REF | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0099 | REF | REF | PTGER3_chr1_70965782_71052816 | PTGER3 | chr1 | 70965782 | 71052816 |
| 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 | a0004 | 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 | a0005 | 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 | a0006 | 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 |
| 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 | a0001c0004a0005c0010 | 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 |
| 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 | a0001c0001t0002a0001c0001t0003a0001c0004t0002others(3): Show | 98 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(95): 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 |
| 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 | a0001c0001t0001g0073a0001c0001t0001g0281a0001c0001t0001g0283others(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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | 59 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(56): 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 | a0001c0001t0001g0289 | 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 | a0001c0001t0001g0092 | 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 | a0001c0002t0006g0335 | 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 | a0001c0001t0002g0054 | 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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1170-676A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70972409 | ||||||
| chr1:70972417
|
C | T | 354 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): 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 | a0001c0001t0002g0312 | 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 | a0001c0001t0002g0074a0001c0001t0002g0322a0003c0005t0002g0296others(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 | a0001c0001t0004g0071a0001c0001t0004g0287 | 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 | a0001c0002t0001g0334 | 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 | a0001c0001t0001g0116a0001c0001t0001g0137a0001c0001t0001g0220 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0005g0106a0001c0001t0005g0282 | 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 | a0001c0001t0001g0220 | 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 |
191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(188): 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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | a0001c0001t0001g0144a0001c0002t0001g0338a0001c0002t0001g0345others(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 | a0001c0001t0001g0154a0001c0002t0001g0337a0001c0002t0001g0342 | 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 | 10 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0295others(7): Show | 10 | HG01071.hp2 HG01168.hp2 HG01169.hp2 others(7): 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 | 261 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(258): 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 | a0001c0001t0001g0023a0001c0001t0001g0095a0001c0001t0001g0267others(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 | a0001c0001t0001g0278a0001c0009t0007g0346 | 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 | a0001c0001t0001g0019a0001c0001t0001g0066a0001c0001t0001g0196others(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 | a0001c0001t0001g0238 | 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 | a0001c0002t0010g0361 | 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 | a0001c0001t0001g0221a0001c0001t0001g0235a0001c0001t0001g0257others(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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(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 | a0001c0001t0001g0275a0001c0002t0001g0344a0002c0003t0001g0247 | 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0221a0001c0001t0001g0235a0001c0001t0001g0257others(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 | a0001c0001t0001g0220a0001c0001t0001g0242a0001c0001t0001g0249others(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 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0068others(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 | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(98): Show | 105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): 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 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0085others(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 | a0001c0001t0001g0236a0001c0001t0001g0237 | 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 | a0001c0001t0005g0282 | 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 | a0001c0001t0005g0106 | 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 | a0001c0001t0002g0072a0004c0008t0002g0036 | 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 | a0001c0002t0010g0361 | 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 | 93 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0020others(90): Show | 94 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1169+452G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 3/3 | chr1 | 70973845 | ||||||
| chr1:70973907
|
G | A | 93 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0020others(90): Show | 94 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(91): 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 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0039others(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 | 94 | a0001c0001t0001g0098a0001c0001t0002g0002a0001c0001t0002g0017others(91): Show | 95 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(92): 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 | a0001c0001t0001g0137 | 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 | 4 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0166others(1): Show | 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 | a0001c0001t0002g0074a0001c0001t0002g0322a0003c0005t0002g0296others(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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0079others(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 | 191 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(188): 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 | a0001c0001t0001g0058a0001c0001t0001g0076a0001c0001t0001g0083others(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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0018 | 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 | 99 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0020others(96): Show | 100 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1078-977delA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70975364 | ||||||
| chr1:70975410
|
C | G | 99 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0020others(96): Show | 100 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(97): 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 | a0001c0001t0004g0071 | 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 | a0002c0003t0001g0201a0002c0003t0001g0232 | 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 | a0001c0001t0001g0105a0001c0002t0001g0337a0001c0002t0001g0338others(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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | 146 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(143): 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | 63 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(60): 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 | a0001c0002t0010g0361 | 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 | 305 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0198 | 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 | 3 | a0001c0001t0001g0227a0001c0001t0001g0234a0001c0001t0001g0235 | 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 | a0001c0001t0001g0079 | 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | 290 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 298 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1078-2386A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976774 | ||||||
| chr1:70976943
|
T | C | 90 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0057others(87): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1078-2555A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70976943 | ||||||
| chr1:70977000
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1078-2612A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977000 | ||||||
| chr1:70977029
|
T | G | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0004t0002g0350 | 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 | a0001c0001t0001g0018 | 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 | a0001c0001t0002g0312 | 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 | a0001c0001t0001g0097 | 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 | 339 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(336): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1078-2900A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977288 | ||||||
| chr1:70977383
|
C | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(205): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1078-2995G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977383 | ||||||
| chr1:70977400
|
T | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0002t0006g0335 | 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 | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1078-3056T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977444 | ||||||
| chr1:70977452
|
T | G | 90 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0057others(87): Show | 91 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.1078-3064A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70977452 | ||||||
| chr1:70977467
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0004g0071 | 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 | 315 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(312): Show | 323 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(320): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0270 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0057others(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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0004g0071 | 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 | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): 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 | a0001c0001t0004g0071 | 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 | a0001c0001t0001g0105a0001c0002t0001g0337a0001c0002t0001g0338others(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 | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0001t0002g0029 | 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 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0113a0001c0001t0002g0114 | 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 | a0001c0001t0001g0058a0001c0001t0001g0076a0001c0001t0001g0083others(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 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0098others(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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | 316 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(313): Show | 324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1078-5113dupC | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70979500 | ||||||
| chr1:70979531
|
T | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0222 | 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 | a0001c0001t0002g0075a0001c0001t0002g0194 | 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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | a0001c0001t0001g0084a0001c0001t0001g0111a0001c0001t0001g0259 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0001t0001g0105a0001c0002t0001g0337a0001c0002t0001g0338others(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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1078-5657delC | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70980044 | ||||||
| chr1:70980082
|
AAAG | A | 9 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | 104 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(101): 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 | a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0197others(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 | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): 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 | a0001c0001t0001g0061 | 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 | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): 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 | a0001c0001t0002g0043 | 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 | a0001c0001t0002g0308a0001c0001t0002g0310a0001c0001t0002g0313others(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 | a0001c0001t0001g0014a0001c0001t0001g0086a0001c0001t0001g0126others(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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0211a0001c0001t0002g0113a0001c0002t0001g0329 | 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0144others(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 | 200 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): 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 | a0001c0001t0001g0032a0001c0001t0001g0118a0001c0001t0001g0145others(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 | 45 | a0001c0001t0001g0006a0001c0001t0001g0049a0001c0001t0001g0079others(42): 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 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0058others(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 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0083others(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 | a0001c0001t0001g0133a0001c0001t0001g0140a0001c0001t0002g0028others(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 | 19 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0185others(16): Show | 19 | HG00544.hp1 HG00609.hp2 HG01168.hp2 others(16): 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 | a0001c0001t0001g0023a0001c0001t0001g0073a0001c0001t0002g0002others(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 | a0001c0001t0002g0243 | 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 | a0001c0001t0002g0075 | 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 | a0001c0004t0002g0348 | 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 | a0001c0001t0002g0021 | 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 | a0001c0001t0002g0322 | 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 | a0001c0004t0002g0348 | 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 | a0001c0001t0001g0321 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0087a0001c0001t0001g0100a0001c0001t0001g0166 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0137others(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 | a0001c0001t0001g0220a0001c0002t0001g0339a0001c0002t0001g0340others(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 | a0001c0002t0001g0336a0001c0002t0001g0338a0001c0002t0001g0343 | 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 | a0001c0002t0001g0344a0001c0004t0002g0347 | 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 | a0001c0001t0001g0105a0001c0004t0002g0349a0001c0004t0002g0350others(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 | a0001c0001t0001g0168 | 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 | a0001c0001t0004g0071 | 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 | a0006c0006t0001g0011 | 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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0008a0001c0001t0001g0059a0001c0001t0001g0206 | 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 | a0001c0001t0002g0027 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0323 | 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 | a0001c0001t0001g0062a0001c0001t0001g0221a0001c0001t0001g0242others(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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172 | 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 | a0001c0001t0001g0098 | 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 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0001t0001g0063others(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 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0006g0335 | 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0005g0106a0001c0002t0001g0334a0003c0005t0002g0297 | 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 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0097others(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 | a0001c0001t0001g0216a0001c0001t0001g0276a0001c0001t0001g0315 | 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 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0019others(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 | a0001c0002t0001g0328a0001c0002t0001g0331 | 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 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0118others(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 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0002t0001g0337 | 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 | a0001c0001t0001g0014a0001c0001t0001g0231 | 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 | a0001c0001t0001g0199a0001c0001t0001g0208a0001c0001t0001g0209others(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 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0088others(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 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0065others(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 | a0001c0001t0001g0069a0001c0001t0001g0210a0001c0001t0001g0211others(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 | a0001c0001t0002g0074 | 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 | 15 | a0001c0001t0001g0087a0001c0001t0001g0092a0001c0001t0001g0096others(12): 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0203others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0065others(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 | a0001c0001t0002g0080 | 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 | 313 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(310): Show | 321 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(318): 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | 209 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1078-7374A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70981762 | ||||||
| chr1:70981836
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0004g0071 | 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 | 312 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(309): Show | 320 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(317): 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 | a0001c0001t0002g0129 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0001g0137a0001c0001t0001g0220a0001c0002t0001g0010others(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 | a0001c0001t0002g0302a0001c0001t0002g0304a0001c0001t0002g0326 | 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 | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): 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 | a0001c0001t0003g0355 | 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 | 17 | a0001c0001t0002g0294a0001c0001t0002g0295a0001c0001t0002g0305others(14): Show | 17 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(14): 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0261 | 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 | a0001c0002t0001g0337 | 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 | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1078-8708C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983096 | ||||||
| chr1:70983215
|
T | C | 88 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(85): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(86): 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 | a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): 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 | 90 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(87): 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 | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1078-9059A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70983447 | ||||||
| chr1:70983757
|
TTG | T | 88 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(85): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(86): 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 | a0001c0001t0001g0321a0001c0001t0002g0322a0003c0005t0002g0296others(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 | a0001c0001t0004g0287 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0001g0279 | 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 | a0001c0001t0004g0071 | 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 | a0001c0002t0010g0361 | 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 | a0001c0001t0002g0075 | 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 | 101 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(98): 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 | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1078-9999delT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70984386 | ||||||
| chr1:70984451
|
A | G | 1 | a0001c0001t0001g0277 | 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 | a0001c0001t0002g0020a0001c0001t0002g0030a0001c0001t0002g0050others(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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0231a0001c0001t0001g0270a0001c0001t0002g0026others(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 | a0001c0001t0001g0276 | 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 | a0001c0001t0002g0080 | 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 | 88 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(85): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(86): 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 | a0001c0001t0001g0176a0001c0001t0001g0265 | 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 | a0001c0001t0001g0236a0001c0001t0001g0237 | 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 | 122 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(119): Show | 123 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(120): 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | a0001c0001t0001g0236a0001c0001t0001g0237 | 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 | a0001c0001t0001g0249 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0002g0045 | 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 | 90 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(87): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0112a0001c0001t0001g0125a0001c0001t0001g0133others(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 | a0001c0002t0010g0361 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0137a0001c0001t0001g0220a0001c0002t0001g0010others(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 | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(2): 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(112): 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 | a0001c0001t0004g0071 | 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 | 95 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(92): Show | 96 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(93): 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 | a0001c0001t0001g0236a0001c0001t0001g0237 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | 88 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(85): Show | 89 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1078-14281G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70988669 | ||||||
| chr1:70988690
|
A | T | 90 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(87): 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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0008g0142 | 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | a0001c0001t0002g0316 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0001c0001t0001g0161 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0116a0001c0001t0001g0189 | 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 | a0004c0008t0002g0036 | 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 | a0001c0001t0001g0081a0001c0001t0001g0137a0001c0001t0001g0220others(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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 223 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(220): 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0199a0001c0001t0001g0217 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0005g0106 | 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 | a0001c0001t0002g0080 | 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 | a0001c0002t0001g0345 | 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 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(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 | a0004c0008t0002g0036 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | 78 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(75): 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 | a0001c0001t0001g0081a0001c0001t0001g0137a0001c0001t0001g0199others(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 | 3 | a0001c0001t0001g0227a0001c0001t0001g0234a0001c0001t0001g0235 | 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 | a0001c0001t0001g0089a0001c0001t0001g0090a0002c0003t0001g0232 | 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 | a0001c0001t0001g0018a0001c0001t0002g0021a0001c0001t0002g0022others(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 | a0001c0001t0001g0018a0001c0001t0001g0105a0001c0001t0002g0017others(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 | a0001c0001t0001g0238a0001c0001t0002g0107a0001c0004t0002g0347others(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 | a0001c0001t0002g0020a0001c0001t0002g0104a0001c0001t0002g0299others(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 | 20 | a0001c0001t0002g0024a0001c0001t0002g0093a0001c0001t0002g0103others(17): Show | 20 | HG00544.hp1 HG01071.hp2 HG01109.hp1 others(17): 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 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0047others(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 | a0001c0001t0001g0018a0001c0001t0001g0105a0001c0001t0001g0321others(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 | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(103): 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 | 16 | a0001c0001t0001g0058a0001c0001t0001g0073a0001c0001t0001g0081others(13): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0002g0205 | 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 | 192 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(189): Show | 195 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(192): 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0003g0359 | 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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | a0001c0001t0002g0072a0004c0008t0002g0036 | 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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0002g0322 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0161a0001c0001t0001g0198 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254others(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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0001g0264 | 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 | 342 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(339): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(101): 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 | 96 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(93): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): 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 | a0001c0001t0001g0067a0001c0001t0001g0214a0001c0001t0001g0228others(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 | a0001c0001t0001g0149a0001c0001t0001g0150 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0221 | 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 | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 204 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1078-18787A>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993175 | ||||||
| chr1:70993365
|
G | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(313): Show | 324 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1077+18940C>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993365 | ||||||
| chr1:70993367
|
G | A | 96 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(93): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1077+18938C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70993367 | ||||||
| chr1:70993368
|
C | T | 96 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(93): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0002g0322others(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 | a0001c0002t0001g0339 | 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 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339others(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 | a0001c0001t0001g0176a0001c0001t0001g0265 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0002g0301 | 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 | a0001c0001t0001g0073a0001c0001t0001g0236a0001c0001t0001g0237others(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 | a0001c0001t0002g0107a0001c0001t0003g0354a0001c0001t0003g0355others(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 | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1077+17843dupA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70994461 | ||||||
| chr1:70994496
|
C | T | 1 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0110 | 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 | 16 | a0001c0001t0002g0295a0001c0001t0002g0305a0001c0001t0002g0306others(13): Show | 16 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(13): 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0133 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0130a0001c0001t0001g0188 | 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 | a0001c0001t0001g0220 | 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(101): 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 | 14 | a0001c0001t0001g0315a0001c0001t0002g0295a0001c0001t0002g0308others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1077+16676A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70995629 | ||||||
| chr1:70995642
|
G | A | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | a0001c0001t0001g0082 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0004g0287 | 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 | a0001c0001t0002g0025a0001c0001t0002g0026 | 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 | a0001c0001t0002g0025a0001c0001t0002g0026 | 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 | 66 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(63): 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 | 6 | a0001c0001t0001g0171a0001c0001t0001g0286a0001c0001t0001g0323others(3): 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 | a0001c0001t0001g0172a0001c0001t0001g0199a0001c0001t0001g0211others(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 | a0001c0001t0001g0073a0001c0001t0001g0081a0001c0001t0001g0213others(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 | a0001c0001t0001g0170a0001c0001t0001g0276a0001c0001t0002g0322others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0051a0001c0001t0001g0078a0001c0001t0001g0089others(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 |
52 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0076others(49): 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 |
92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): 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 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0084others(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 | a0001c0001t0001g0057a0001c0001t0001g0130a0001c0001t0001g0196others(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 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0185 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0321 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0002g0322 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0003g0354a0001c0001t0003g0355a0001c0001t0003g0356others(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 | 111 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(108): 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 | a0001c0002t0001g0334 | 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 | a0001c0001t0001g0073 | 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 | a0001c0001t0001g0073 | 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 | a0001c0002t0001g0338a0001c0002t0001g0339a0001c0002t0001g0340others(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 | 100 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(97): 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 | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0002g0322 | 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 | a0001c0001t0001g0209 | 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0003g0354 | 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 | a0001c0002t0001g0328a0001c0002t0001g0329a0001c0002t0001g0330others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0002g0046 | 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 | 338 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0005g0106 | 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 | 97 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(94): Show | 98 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(95): 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 | a0001c0002t0006g0335 | 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 | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(92): 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 | a0001c0001t0001g0242 | 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 | 337 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1077+12782T>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 70999523 | ||||||
| chr1:70999609
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): 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 | 5 | a0001c0001t0001g0047a0001c0001t0001g0286a0001c0001t0001g0323others(2): 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0220 | 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 | 99 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(96): 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 | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0001g0091 | 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 | 17 | a0001c0001t0001g0315a0001c0001t0002g0295a0001c0001t0002g0305others(14): Show | 17 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(14): 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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | a0001c0001t0005g0106 | 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 | a0001c0001t0001g0073a0001c0001t0001g0281a0001c0001t0001g0283others(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 | a0001c0001t0002g0107a0001c0001t0003g0354a0001c0001t0003g0355others(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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0084 | 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 | a0001c0001t0002g0322 | 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 | 337 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1077+9536C>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 2/3 | chr1 | 71002769 | ||||||
| chr1:71002810
|
A | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(105): 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0016 | 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 | a0001c0001t0002g0025a0001c0001t0002g0026 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0023 | 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 | 100 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(97): 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0047a0001c0001t0002g0103a0001c0001t0002g0104others(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 | 104 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(101): Show | 105 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(102): 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 | a0001c0001t0005g0106 | 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 | a0001c0001t0001g0186 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(202): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): 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 | a0001c0001t0004g0287 | 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 | a0001c0009t0007g0346 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0132 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0039others(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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | 99 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(96): 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0001g0264a0001c0001t0001g0278 | 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0001g0165 | 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 | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): 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 | a0001c0001t0001g0260 | 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 | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(202): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): 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 | 340 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(337): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): 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 | a0001c0001t0002g0048 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0002g0309a0001c0001t0002g0311 | 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 | 5 | a0001c0001t0001g0004a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 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 | a0001c0001t0004g0071 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0002g0320 | 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 | a0001c0001t0001g0122 | 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 | 100 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(97): 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0002g0021a0001c0001t0002g0053 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | 104 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(101): Show | 105 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(102): 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0149a0001c0001t0001g0150 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | 104 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(101): Show | 105 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(102): 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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0001c0001t0004g0287 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0001g0207 | 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 | a0001c0002t0001g0338a0001c0002t0001g0339a0001c0002t0001g0340others(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 | a0001c0001t0001g0073a0001c0001t0001g0281a0001c0001t0001g0283others(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 | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): 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 | a0001c0001t0001g0168 | 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 | a0001c0002t0010g0361 | 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 | a0001c0001t0001g0006 | 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 | 205 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(202): Show | 208 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(205): 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | a0001c0001t0001g0008 | 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 | a0001c0001t0002g0080 | 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 | 92 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(89): 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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | a0001c0001t0001g0242 | 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 | 337 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.898-425G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71012909 | ||||||
| chr1:71012925
|
ATAT | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(332): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): 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 | a0001c0001t0002g0322 | 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 | a0001c0001t0001g0149a0001c0004t0002g0347a0001c0004t0002g0348others(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 | a0001c0001t0004g0287 | 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 | a0001c0001t0001g0213a0001c0001t0001g0229a0001c0001t0001g0231others(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 | a0001c0002t0010g0361 | 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 | a0001c0001t0001g0111a0001c0001t0001g0132a0001c0001t0001g0182others(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 | a0001c0001t0001g0105a0001c0001t0001g0321a0001c0001t0005g0106 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0027others(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 | a0001c0001t0001g0242 | 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 | a0001c0001t0004g0287 | 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 | a0001c0001t0004g0287 | 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0009t0007g0346 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(97): 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | 338 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.898-2482C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71014966 | ||||||
| chr1:71015115
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0143 | 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 | 131 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(128): 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 | a0001c0001t0001g0089 | 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | 337 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0001g0063 | 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 | a0001c0009t0007g0346 | 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 | a0001c0001t0004g0287 | 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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0149a0001c0001t0001g0150 | 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 | a0001c0001t0001g0208a0001c0001t0001g0230a0001c0001t0001g0239others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0323 | 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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0276 | 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 | 111 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(108): 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 | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(95): 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | a0001c0001t0001g0241 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0002t0006g0335 | 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 | a0001c0001t0001g0081 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(230): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0236a0001c0001t0001g0237 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0005g0106 | 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0001t0001g0237 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0002c0003t0001g0202 | 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 | a0001c0001t0003g0354 | 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 | a0001c0001t0001g0315 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(101): 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0079others(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 | a0001c0001t0001g0321 | 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 | 337 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0002g0322 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0002t0001g0345 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0290 | 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 | a0001c0002t0006g0335 | 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 | 103 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(100): Show | 104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | 329 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(326): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0001g0006a0001c0001t0001g0196 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0002t0001g0331 | 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 | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(98): 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0208a0001c0001t0001g0230a0001c0001t0001g0239others(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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | 333 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.898-7944A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020428 | ||||||
| chr1:71020485
|
T | C | 338 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.898-8001A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71020485 | ||||||
| chr1:71020519
|
G | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(98): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0073a0001c0001t0001g0281a0001c0001t0001g0283others(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 | 88 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(85): 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 | a0001c0001t0001g0008a0001c0001t0001g0059a0001c0001t0001g0066others(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 | a0001c0001t0001g0065a0001c0001t0001g0081a0001c0001t0001g0209others(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 | a0001c0001t0001g0321 | 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 | a0003c0005t0002g0296 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0218 | 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 | 101 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(98): Show | 102 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(99): 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 | a0001c0001t0002g0026 | 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 | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0286others(3): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0002t0001g0332a0001c0002t0001g0336 | 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 | a0001c0001t0001g0176a0001c0001t0001g0265 | 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 | a0001c0002t0001g0337a0001c0002t0001g0341a0001c0002t0001g0342others(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 | 103 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(100): Show | 104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.898-8888T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021372 | ||||||
| chr1:71021432
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | a0001c0001t0001g0264a0001c0001t0001g0278 | 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 | a0001c0001t0001g0008 | 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 | a0001c0001t0002g0075 | 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 | a0001c0001t0005g0106 | 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | 331 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(328): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.898-9218C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71021702 | ||||||
| chr1:71021710
|
C | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0002t0001g0332 | 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 | 103 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(100): Show | 104 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(101): 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 | a0001c0001t0001g0242 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0003c0005t0002g0296 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 113 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(110): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0220a0001c0002t0001g0010a0001c0002t0001g0328others(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 | a0001c0001t0001g0264 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0002g0020 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0263 | 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 | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): 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 | 9 | a0001c0001t0001g0315a0001c0001t0002g0295a0001c0001t0002g0309others(6): Show | 9 | HG01071.hp2 HG01168.hp2 HG01169.hp2 others(6): 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 | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0171 | 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 | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): 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 | a0001c0002t0001g0328a0001c0002t0001g0329a0001c0002t0001g0330others(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 | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): 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 | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(100): 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 | a0001c0001t0002g0038 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0239 | 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 | 90 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(87): 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 | 194 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(191): Show | 197 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.898-11085G>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71023569 | ||||||
| chr1:71023596
|
A | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(101): 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 | a0001c0001t0002g0046 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | 108 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(105): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0073a0001c0001t0001g0173a0001c0001t0001g0190others(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 | a0001c0002t0001g0334 | 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 | a0001c0001t0001g0087 | 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 | a0001c0001t0002g0318 | 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 | 330 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.898-11679A>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71024163 | ||||||
| chr1:71024291
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | 194 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(191): Show | 197 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(194): 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0002g0322 | 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 | a0001c0001t0004g0287 | 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 | 27 | a0001c0001t0001g0092a0001c0001t0001g0268a0001c0001t0001g0286others(24): 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 | 92 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(89): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0002g0204a0001c0001t0002g0205 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0263 | 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 | a0001c0001t0001g0073a0001c0001t0005g0106 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | 28 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(25): 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 | 119 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(116): Show | 121 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(118): 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0004g0287 | 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 | a0001c0001t0001g0105a0001c0001t0001g0321 | 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 | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(91): 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 |
162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(159): 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 |
36 | a0001c0001t0001g0058a0001c0001t0001g0076a0001c0001t0001g0105others(33): Show | 36 | HG00099.hp2 HG00738.hp1 HG01109.hp1 others(33): 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 | a0001c0001t0001g0081a0001c0001t0001g0292a0001c0001t0001g0293others(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 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(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 | a0001c0001t0005g0106 | 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 | a0001c0001t0001g0073 | 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 | 27 | a0001c0001t0001g0315a0001c0001t0002g0159a0001c0001t0002g0160others(24): Show | 27 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(24): 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | a0001c0001t0002g0309 | 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 | a0001c0001t0001g0254 | 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | a0001c0001t0002g0243 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0109 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0209 | 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 | 19 | a0001c0001t0001g0315a0001c0001t0002g0159a0001c0001t0002g0160others(16): Show | 19 | HG01071.hp2 HG01109.hp1 HG01167.hp1 others(16): 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 | a0001c0002t0001g0328a0001c0002t0001g0329a0001c0002t0001g0330others(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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0064 | 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 | 128 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(125): Show | 130 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.898-13723T>A | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71026207 | ||||||
| chr1:71026242
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0118a0001c0001t0001g0195 | 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | 7 | a0001c0001t0001g0315a0001c0001t0002g0295a0001c0001t0002g0314others(4): Show | 7 | HG01071.hp2 HG01496.hp2 HG01952.hp2 others(4): 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0073a0001c0001t0004g0287a0001c0001t0005g0106 | 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 | a0001c0001t0002g0280 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0002g0044 | 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0001g0073a0001c0001t0005g0106 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0110 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0081 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0281a0001c0001t0005g0282 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0073a0001c0001t0004g0287a0001c0001t0005g0106 | 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 | 105 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(102): 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 | a0001c0001t0001g0264 | 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 | 121 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(118): Show | 123 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.898-15472A>G | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71027956 | ||||||
| chr1:71028009
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(333): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0105a0001c0001t0004g0071 | 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 | a0001c0001t0001g0291 | 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 | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(2): 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0082 | 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 | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(104): 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 | a0001c0001t0002g0308 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(5): 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 | a0001c0001t0001g0085 | 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 | a0001c0002t0001g0333 | 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 | a0001c0001t0002g0322 | 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 | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | 333 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): 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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0002g0322 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0057 | 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 | a0001c0001t0001g0209 | 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 | 84 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0013others(81): 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 | a0001c0001t0001g0008a0001c0001t0001g0105a0001c0001t0001g0206others(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 | a0001c0001t0001g0199a0001c0001t0001g0277a0001c0001t0001g0291others(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 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(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 | 37 | a0001c0001t0001g0073a0001c0001t0001g0086a0001c0001t0001g0087others(34): 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 | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(113): 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 | 14 | a0001c0001t0001g0315a0001c0001t0002g0295a0001c0001t0002g0308others(11): Show | 14 | HG01071.hp2 HG01109.hp1 HG01168.hp2 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 | ||||||
| chr1:71029955
|
A | T | 1 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0057others(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 | a0001c0001t0001g0023a0001c0001t0002g0002a0001c0001t0002g0022others(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 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0197others(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 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0057others(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 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0197others(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 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0057others(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 | a0001c0001t0001g0023a0001c0001t0002g0002a0001c0001t0002g0022others(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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0047a0001c0001t0001g0284a0001c0001t0001g0285others(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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0105 | 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 | 338 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0004g0287 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0073a0001c0001t0005g0106 | 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0002g0021 | 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 | 126 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(123): Show | 128 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.897+15844dupA | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71030836 | ||||||
| chr1:71031245
|
AAC | A | 35 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0082others(32): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): 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 | 36 | a0001c0001t0001g0081a0001c0001t0001g0152a0001c0001t0001g0189others(33): Show | 36 | HG00621.hp1 HG01071.hp2 HG01109.hp1 others(33): 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 | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(95): 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 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0098 | 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 | a0001c0001t0003g0354 | 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 | a0001c0002t0001g0345 | 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 | a0001c0001t0001g0258 | 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 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339others(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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0118a0001c0001t0001g0195 | 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 | a0001c0001t0002g0074 | 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 | 94 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(91): 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 | a0001c0001t0002g0045 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(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 | 4 | a0001c0001t0001g0286a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0002t0001g0328a0001c0002t0001g0329a0001c0002t0001g0330others(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 | a0001c0001t0001g0213 | 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 | a0001c0002t0001g0341 | 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 | a0001c0001t0001g0173a0001c0001t0001g0190a0001c0001t0001g0298 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0002t0006g0335 | 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0007 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0001g0279 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0018a0001c0001t0001g0023a0001c0001t0001g0032others(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 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0051others(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 | a0001c0001t0002g0159a0001c0001t0002g0160 | 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 | a0001c0001t0002g0294 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0001g0212a0001c0001t0001g0267 | 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 | a0001c0001t0001g0016a0001c0001t0001g0116a0001c0001t0001g0117others(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 | a0001c0001t0001g0073a0001c0001t0005g0106 | 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 | 129 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(126): Show | 131 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.897+10299C>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036382 | ||||||
| chr1:71036407
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(98): 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 | a0001c0002t0006g0335 | 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 | 335 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(332): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.897+10118G>T | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036563 | ||||||
| chr1:71036567
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(194): 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 | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(172): 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 | a0001c0001t0001g0158 | 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 | a0001c0002t0001g0338 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0002t0001g0332a0001c0002t0001g0336a0003c0005t0002g0296others(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 | a0001c0002t0001g0332a0001c0002t0001g0336a0003c0005t0002g0296others(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 | a0001c0001t0001g0018 | 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 | a0001c0001t0003g0360 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.897+9857T>C | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71036824 | ||||||
| chr1:71036838
|
C | CA | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(98): 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 | 317 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): 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 | a0001c0001t0001g0105 | 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 | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(99): 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 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0005g0282others(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 | a0001c0001t0002g0074 | 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 | a0001c0001t0002g0020 | 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 | a0001c0001t0002g0074 | 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 | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(106): 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0074 | 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 | 226 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(223): Show | 230 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(227): 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 | a0001c0001t0002g0074 | 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 | a0001c0002t0001g0338a0001c0002t0001g0339a0001c0002t0001g0340others(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 | 225 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(222): Show | 229 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(226): 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 | a0001c0001t0001g0089a0001c0001t0001g0090 | 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 | a0001c0001t0001g0085a0001c0001t0001g0108a0001c0001t0001g0109others(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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0005g0282others(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 | a0001c0001t0002g0048 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0177 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0001g0073a0001c0001t0005g0106 | 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 | 330 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(327): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0211 | 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 | 124 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(121): Show | 126 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(123): 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0018 | 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 | 5 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(2): 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 | a0001c0001t0002g0205 | 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 | a0001c0001t0001g0210 | 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 | a0003c0005t0002g0296a0003c0005t0002g0297 | 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 | a0001c0001t0001g0276 | 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 | a0001c0002t0006g0335 | 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 | a0001c0001t0001g0081a0001c0001t0001g0276a0001c0001t0004g0287others(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 | a0001c0001t0001g0163 | 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 | a0001c0002t0001g0332a0001c0002t0001g0336 | 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 | 51 | a0001c0001t0001g0081a0001c0001t0001g0161a0001c0001t0001g0162others(48): Show | 51 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.897+7031dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71039649 | ||||||
| chr1:71039649
|
CAAAAAAA | C | 7 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0001g0115 | 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 | 150 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(147): 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 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0263 | 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 | a0001c0001t0001g0081a0001c0001t0004g0287 | 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 | a0001c0001t0001g0058a0001c0001t0001g0076 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(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 | a0001c0001t0002g0074 | 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 | a0001c0002t0001g0337a0001c0002t0001g0338a0001c0002t0001g0339others(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 | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(92): 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 | a0001c0001t0001g0250a0001c0001t0001g0288a0001c0001t0001g0289others(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 | a0001c0001t0001g0083a0001c0001t0001g0163a0001c0001t0001g0164others(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 | 48 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(45): Show | 48 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(45): 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 | a0001c0001t0002g0294 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0279 | 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 | 86 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(83): 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0250 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0002g0046 | 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 | a0001c0001t0001g0112 | 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 | a0001c0001t0002g0320 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0084a0001c0001t0001g0110a0001c0001t0001g0111 | 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 | a0001c0001t0001g0208a0001c0001t0001g0251 | 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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0175 | 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 | 354 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(351): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): 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 | a0001c0001t0002g0017 | 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 | a0001c0001t0002g0197 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0203a0001c0001t0001g0252a0001c0001t0001g0253others(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 | a0001c0001t0001g0083a0001c0001t0001g0174 | 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 | 338 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0002g0074 | 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 | a0001c0001t0001g0198 | 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 | 253 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(250): 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 | a0001c0002t0001g0010 | 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 | a0001c0001t0001g0198 | 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | a0001c0002t0001g0331 | 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 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0002g0107others(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 | a0001c0001t0001g0203a0001c0001t0001g0252a0001c0001t0001g0253others(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 | a0001c0001t0001g0203a0001c0001t0001g0252a0001c0001t0001g0253others(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 | 38 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(35): Show | 38 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(35): 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 | a0001c0001t0001g0105 | 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 | a0001c0002t0001g0010a0001c0002t0001g0328a0001c0002t0001g0329others(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 | a0001c0002t0001g0328a0001c0002t0001g0329a0001c0002t0001g0330others(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 | a0001c0001t0002g0048 | 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 | a0001c0001t0001g0259 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | a0001c0001t0001g0081 | 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 | 33 | a0001c0001t0001g0049a0001c0001t0001g0081a0001c0001t0001g0165others(30): Show | 33 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.897+2241dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71044439 | ||||||
| chr1:71044439
|
CA | C | 8 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0260a0001c0001t0001g0261 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0009a0001c0001t0001g0262a0001c0001t0001g0263 | 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 | 291 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(288): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): 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 | a0001c0001t0002g0074 | 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 | 10 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(7): 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 | a0001c0001t0002g0075 | 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 | a0001c0004t0002g0347a0001c0004t0002g0348a0001c0004t0002g0349others(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 | 97 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(94): 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 | 338 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0001g0321 | 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 | a0001c0004t0002g0347 | 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 | 338 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(335): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0001g0105a0001c0001t0001g0279a0001c0001t0002g0103others(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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(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 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0280 | 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 | 47 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(44): Show | 47 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(44): 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 | a0001c0001t0001g0105 | 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 | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.897+395dupT | PTGER3 | ENSG00000050628.21 | transcript | ENST00000306666.10 | protein_coding | 1/3 | chr1 | 71046285 | ||||||
| chr1:71046285
|
C | CAA | 50 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(47): 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 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0002g0197others(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 | 58 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(55): 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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0023others(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 | 97 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0012others(94): 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 | a0001c0001t0001g0016 | 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 | 47 | a0001c0001t0001g0281a0001c0001t0001g0283a0001c0001t0001g0284others(44): Show | 47 | HG00639.hp2 HG01071.hp2 HG01109.hp1 others(44): 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 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(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 |