Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5027 |
|---|---|
| ensemblid | ENSG00000089041.17 |
| hgncid | 8537 |
| symbol | P2RX7 |
| name | purinergic receptor P2X 7 |
| refseq_nuc | NM_002562.6 |
| refseq_prot | NP_002553.3 |
| ensembl_nuc | ENST00000328963.10 |
| ensembl_prot | ENSP00000330696.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 121132876 |
| end | 121188032 |
| strand | + |
| ver | v1.2 |
| region | chr12:121132876-121188032 |
| region5000 | chr12:121127876-121193032 |
| regionname0 | P2RX7_chr12_121132876_121188032 |
| regionname5000 | P2RX7_chr12_121127876_121193032 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 595 | 51 | 9 | 8 | 25 | 5 | 3 | 19 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002 | 0/0 | 595 | 44 | 20 | 5 | 17 | 1 | 1 | 15 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0003 | 0/0 | 595 | 40 | 2 | 8 | 29 | 0 | 1 | 20 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004 | 0/0 | 595 | 39 | 11 | 5 | 14 | 3 | 6 | 10 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005 | 0/0 | 595 | 24 | 10 | 4 | 8 | 1 | 1 | 8 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006 | 0/0 | 595 | 24 | 3 | 12 | 6 | 0 | 3 | 5 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0007 | 0/0 | 595 | 21 | 4 | 3 | 7 | 0 | 7 | 5 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0008 | 0/0 | 595 | 19 | 0 | 1 | 14 | 1 | 3 | 9 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0009 | 0/0 | 595 | 12 | 0 | 0 | 12 | 0 | 0 | 12 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0010 | 0/0 | 595 | 10 | 0 | 4 | 6 | 0 | 0 | 6 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0011 | 0/0 | 595 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0012 | 0/0 | 595 | 9 | 1 | 4 | 0 | 1 | 3 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0013 | 0/0 | 595 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0014 | 1/0 | 595 | 8 | 0 | 1 | 4 | 2 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015 | 0/0 | 595 | 8 | 3 | 2 | 2 | 0 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0016 | 0/0 | 595 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0017 | 0/0 | 595 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0018 | 0/0 | 595 | 3 | 1 | 0 | 0 | 0 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0019 | 0/0 | 595 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0020 | 0/0 | 595 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0021 | 0/0 | 595 | 3 | 0 | 1 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0022 | 0/0 | 595 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0023 | 0/0 | 595 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0024 | 0/0 | 595 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0025 | 0/0 | 595 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0026 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0027 | 0/0 | 595 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0028 | 0/0 | 595 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0029 | 0/0 | 595 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0030 | 0/0 | 595 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0031 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0032 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0033 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0034 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0035 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0036 | 0/0 | 595 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1788 | 50 | 8 | 8 | 25 | 5 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0002 | 0/0 | 1788 | 41 | 19 | 4 | 16 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0003 | 0/0 | 1788 | 39 | 11 | 5 | 14 | 3 | 6 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0004 | 0/0 | 1788 | 39 | 2 | 7 | 29 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0005 | 0/0 | 1788 | 24 | 3 | 12 | 6 | 0 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0006 | 0/0 | 1788 | 19 | 5 | 4 | 8 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0007 | 0/0 | 1788 | 18 | 0 | 1 | 13 | 1 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0008 | 0/0 | 1788 | 16 | 4 | 3 | 7 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0009 | 0/0 | 1788 | 12 | 0 | 0 | 12 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0010 | 0/0 | 1788 | 10 | 0 | 4 | 6 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0011 | 0/0 | 1788 | 10 | 8 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0012 | 0/0 | 1788 | 8 | 3 | 2 | 2 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0013 | 0/0 | 1788 | 8 | 0 | 4 | 0 | 1 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0014 | 1/0 | 1788 | 8 | 0 | 1 | 4 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0015 | 0/0 | 1788 | 5 | 0 | 0 | 0 | 0 | 5 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0016 | 0/0 | 1788 | 5 | 5 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0017 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0018 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0019 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0020 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0021 | 0/0 | 1788 | 3 | 0 | 1 | 2 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0022 | 0/0 | 1788 | 3 | 3 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0023 | 0/0 | 1788 | 3 | 0 | 0 | 0 | 1 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0024 | 0/0 | 1788 | 2 | 1 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0025 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0026 | 0/0 | 1788 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0027 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0028 | 0/0 | 1788 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0029 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0030 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0031 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0032 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0033 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0034 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0035 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0036 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0037 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0038 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0039 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0040 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0041 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0042 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0043 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0044 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0045 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0046 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| c0047 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3326 | 154 | 18 | 28 | 82 | 9 | 16 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0002 | 0/0 | 3326 | 46 | 11 | 11 | 19 | 1 | 4 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0003 | 1/0 | 3326 | 32 | 19 | 2 | 8 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0004 | 0/0 | 3326 | 30 | 14 | 1 | 13 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0005 | 0/0 | 3326 | 23 | 13 | 6 | 0 | 1 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0006 | 0/0 | 3326 | 20 | 0 | 0 | 20 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0007 | 0/0 | 3328 | 8 | 8 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0008 | 0/0 | 3326 | 5 | 0 | 0 | 0 | 0 | 5 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0009 | 0/0 | 3326 | 5 | 2 | 1 | 0 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0010 | 0/0 | 3327 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0011 | 0/0 | 3327 | 4 | 0 | 4 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0012 | 0/0 | 3326 | 4 | 0 | 1 | 1 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0013 | 0/0 | 3326 | 3 | 3 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0014 | 0/0 | 3327 | 2 | 0 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0015 | 0/0 | 3327 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0016 | 0/0 | 3326 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0017 | 0/0 | 3326 | 2 | 0 | 0 | 2 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0018 | 0/0 | 3326 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0019 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0020 | 0/0 | 3327 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0021 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0022 | 0/0 | 3326 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0023 | 0/0 | 3326 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0024 | 0/0 | 3326 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0025 | 0/0 | 3325 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0026 | 0/0 | 3326 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0027 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0028 | 0/0 | 3326 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0029 | 0/0 | 3326 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0030 | 0/0 | 3326 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0031 | 0/0 | 3326 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0032 | 0/0 | 3325 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0033 | 0/0 | 3326 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0034 | 0/0 | 3326 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0035 | 0/0 | 3326 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0036 | 0/0 | 3326 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| t0037 | 0/0 | 3326 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1788 | 50 | 8 | 8 | 25 | 5 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0001c0043 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0002 | 0/0 | 1788 | 41 | 19 | 4 | 16 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0024 | 0/0 | 1788 | 2 | 1 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0033 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0003c0004 | 0/0 | 1788 | 39 | 2 | 7 | 29 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0003c0044 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003 | 0/0 | 1788 | 39 | 11 | 5 | 14 | 3 | 6 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0006 | 0/0 | 1788 | 19 | 5 | 4 | 8 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0017 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0038 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005 | 0/0 | 1788 | 24 | 3 | 12 | 6 | 0 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0007c0008 | 0/0 | 1788 | 16 | 4 | 3 | 7 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0007c0015 | 0/0 | 1788 | 5 | 0 | 0 | 0 | 0 | 5 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0008c0007 | 0/0 | 1788 | 18 | 0 | 1 | 13 | 1 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0008c0039 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0009c0009 | 0/0 | 1788 | 12 | 0 | 0 | 12 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0010c0010 | 0/0 | 1788 | 10 | 0 | 4 | 6 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0011c0011 | 0/0 | 1788 | 10 | 8 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0012c0013 | 0/0 | 1788 | 8 | 0 | 4 | 0 | 1 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0012c0042 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0013c0018 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0013c0019 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0014c0014 | 1/0 | 1788 | 8 | 0 | 1 | 4 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015c0012 | 0/0 | 1788 | 8 | 3 | 2 | 2 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0016c0016 | 0/0 | 1788 | 5 | 5 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0017c0020 | 0/0 | 1788 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0018c0026 | 0/0 | 1788 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0018c0034 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0019c0022 | 0/0 | 1788 | 3 | 3 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0020c0023 | 0/0 | 1788 | 3 | 0 | 0 | 0 | 1 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0021c0021 | 0/0 | 1788 | 3 | 0 | 1 | 2 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0022c0025 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0023c0028 | 0/0 | 1788 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0024c0027 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0025c0029 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0026c0030 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0027c0032 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0028c0040 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0029c0037 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0030c0031 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0031c0036 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0032c0035 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0033c0041 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0034c0046 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0035c0045 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0036c0047 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5113 | 46 | 8 | 7 | 23 | 5 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0001c0001t0003 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0001c0001t0017 | 0/0 | 5113 | 2 | 0 | 0 | 2 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0001c0001t0034 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0001c0043t0001 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0002t0001 | 0/0 | 5113 | 17 | 2 | 4 | 9 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0002t0003 | 0/0 | 5113 | 21 | 15 | 0 | 6 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0002t0033 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0002t0035 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0002t0036 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0024t0001 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0024t0003 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0002c0033t0001 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0003c0004t0001 | 0/0 | 5113 | 37 | 1 | 7 | 28 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0003c0004t0003 | 0/0 | 5113 | 2 | 1 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0003c0044t0001 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0004 | 0/0 | 5113 | 16 | 1 | 1 | 13 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0007 | 0/0 | 5115 | 6 | 6 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0008 | 0/0 | 5113 | 5 | 0 | 0 | 0 | 0 | 5 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0010 | 0/0 | 5114 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0011 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0012 | 0/0 | 5113 | 3 | 0 | 1 | 0 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0020 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0027 | 0/0 | 5112 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0031 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0004c0003t0032 | 0/0 | 5112 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0006t0001 | 0/0 | 5113 | 15 | 1 | 4 | 8 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0006t0003 | 0/0 | 5113 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0006t0009 | 0/0 | 5113 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0017t0005 | 0/0 | 5113 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0005c0038t0003 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0002 | 0/0 | 5113 | 15 | 0 | 9 | 5 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0013 | 0/0 | 5113 | 3 | 3 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0018 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0023 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0024 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0026 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0029 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0006c0005t0030 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0007c0008t0001 | 0/0 | 5113 | 16 | 4 | 3 | 7 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0007c0015t0001 | 0/0 | 5113 | 5 | 0 | 0 | 0 | 0 | 5 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0008c0007t0002 | 0/0 | 5113 | 18 | 0 | 1 | 13 | 1 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0008c0039t0028 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0009c0009t0006 | 0/0 | 5113 | 12 | 0 | 0 | 12 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0010c0010t0006 | 0/0 | 5113 | 6 | 0 | 0 | 6 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0010c0010t0011 | 0/0 | 5114 | 3 | 0 | 3 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0010c0010t0025 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0011c0011t0004 | 0/0 | 5113 | 5 | 5 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0011c0011t0005 | 0/0 | 5113 | 5 | 3 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0012c0013t0005 | 0/0 | 5113 | 8 | 0 | 4 | 0 | 1 | 3 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0012c0042t0005 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0013c0018t0004 | 0/0 | 5113 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0013c0019t0004 | 0/0 | 5113 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0014c0014t0001 | 0/0 | 5113 | 6 | 0 | 1 | 3 | 2 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0014c0014t0003 | 1/0 | 5113 | 2 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015c0012t0004 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015c0012t0006 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015c0012t0007 | 0/0 | 5115 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015c0012t0012 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015c0012t0014 | 0/0 | 5114 | 2 | 0 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0015c0012t0019 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0016c0016t0002 | 0/0 | 5113 | 5 | 5 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0017c0020t0002 | 0/0 | 5113 | 4 | 4 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0018c0026t0016 | 0/0 | 5113 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0018c0034t0005 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0019c0022t0005 | 0/0 | 5113 | 3 | 3 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0020c0023t0009 | 0/0 | 5113 | 2 | 0 | 0 | 0 | 1 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0020c0023t0037 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0021c0021t0001 | 0/0 | 5113 | 3 | 0 | 1 | 2 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0022c0025t0015 | 0/0 | 5114 | 2 | 2 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0023c0028t0001 | 0/0 | 5113 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0024c0027t0005 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0024c0027t0021 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0025c0029t0003 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0026c0030t0006 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0027c0032t0009 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0028c0040t0003 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0029c0037t0001 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0030c0031t0002 | 0/0 | 5113 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0031c0036t0002 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0032c0035t0002 | 0/0 | 5113 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0033c0041t0001 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0034c0046t0002 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0035c0045t0022 | 0/0 | 5113 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| a0036c0047t0001 | 0/0 | 5113 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | copy fasta | chr12 | 121127876 | 121193032 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0017g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0001t0034g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0001c0043t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0033g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0035g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0002t0036g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0024t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0024t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0002c0033t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0004t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0003c0044t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0007g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0008g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0008g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0008g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0008g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0010g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0010g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0010g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0011g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0012g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0012g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0012g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0020g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0027g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0031g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0004c0003t0032g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0003g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0006t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0017t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0017t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0017t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0017t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0005c0038t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0018g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0023g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0024g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0026g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0029g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0006c0005t0030g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0008t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0015t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0015t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0015t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0015t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0007c0015t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0007t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0008c0039t0028g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0009c0009t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0006g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0011g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0011g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0011g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0010c0010t0025g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0011c0011t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0013t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0012c0042t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0018t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0018t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0018t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0018t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0019t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0019t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0019t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0013c0019t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0014c0014t0003g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0012g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0014g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0014g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0015c0012t0019g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0016c0016t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0016c0016t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0016c0016t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0016c0016t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0016c0016t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0017c0020t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0017c0020t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0017c0020t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0017c0020t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0018c0026t0016g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0018c0026t0016g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0018c0034t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0019c0022t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0019c0022t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0019c0022t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0020c0023t0009g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0020c0023t0009g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0020c0023t0037g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0021c0021t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0021c0021t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0021c0021t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0022c0025t0015g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0022c0025t0015g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0023c0028t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0024c0027t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0024c0027t0021g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0025c0029t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0026c0030t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0027c0032t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0028c0040t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0029c0037t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0030c0031t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0031c0036t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0032c0035t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0033c0041t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0034c0046t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0035c0045t0022g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| a0036c0047t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00099 | hp2 | a0004 | c0003 | t0004 | g0233 | EUR | GBR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0331 | EUR | GBR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0131 | EUR | GBR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00280 | hp1 | a0004 | c0003 | t0012 | g0199 | EUR | FIN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00280 | hp2 | a0028 | c0040 | t0003 | g0066 | EUR | FIN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00323 | hp1 | a0008 | c0007 | t0002 | g0332 | EUR | FIN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00323 | hp2 | a0020 | c0023 | t0009 | g0160 | EUR | FIN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00438 | hp1 | a0008 | c0007 | t0002 | g0288 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00438 | hp2 | a0003 | c0004 | t0001 | g0163 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00558 | hp2 | a0003 | c0004 | t0001 | g0084 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00621 | hp1 | a0004 | c0003 | t0004 | g0234 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00621 | hp2 | a0008 | c0007 | t0002 | g0305 | EAS | CHS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00642 | hp2 | a0004 | c0003 | t0031 | g0203 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00735 | hp1 | a0005 | c0006 | t0001 | g0001 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00735 | hp2 | a0004 | c0003 | t0012 | g0205 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00741 | hp1 | a0006 | c0005 | t0018 | g0048 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG00741 | hp2 | a0008 | c0007 | t0002 | g0326 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01069 | hp1 | a0007 | c0008 | t0001 | g0010 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01069 | hp2 | a0012 | c0013 | t0005 | g0009 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01071 | hp1 | a0007 | c0008 | t0001 | g0116 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01071 | hp2 | a0003 | c0004 | t0001 | g0050 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01074 | hp2 | a0010 | c0010 | t0011 | g0280 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01099 | hp1 | a0011 | c0011 | t0005 | g0005 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01106 | hp1 | a0005 | c0006 | t0001 | g0082 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01106 | hp2 | a0021 | c0021 | t0001 | g0064 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01109 | hp1 | a0011 | c0011 | t0005 | g0005 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01109 | hp2 | a0027 | c0032 | t0009 | g0037 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0361 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01168 | hp1 | a0004 | c0003 | t0011 | g0133 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01168 | hp2 | a0005 | c0006 | t0001 | g0341 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01169 | hp1 | a0005 | c0006 | t0001 | g0337 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01243 | hp1 | a0004 | c0003 | t0020 | g0245 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01243 | hp2 | a0030 | c0031 | t0002 | g0202 | AMR | PUR | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01255 | hp1 | a0015 | c0012 | t0014 | g0031 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01255 | hp2 | a0003 | c0004 | t0001 | g0026 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01256 | hp1 | a0003 | c0004 | t0001 | g0003 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01257 | hp1 | a0015 | c0012 | t0014 | g0053 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01257 | hp2 | a0010 | c0010 | t0011 | g0279 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01258 | hp1 | a0010 | c0010 | t0011 | g0278 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01258 | hp2 | a0003 | c0004 | t0001 | g0003 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01346 | hp2 | a0006 | c0005 | t0002 | g0044 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01358 | hp1 | a0006 | c0005 | t0002 | g0143 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01358 | hp2 | a0002 | c0024 | t0003 | g0186 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01361 | hp1 | a0003 | c0044 | t0001 | g0049 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01516 | hp1 | a0014 | c0014 | t0001 | g0129 | EUR | IBS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01516 | hp2 | a0005 | c0006 | t0001 | g0001 | EUR | IBS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01517 | hp1 | a0014 | c0014 | t0001 | g0142 | EUR | IBS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01517 | hp2 | a0012 | c0013 | t0005 | g0146 | EUR | IBS | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01884 | hp1 | a0011 | c0011 | t0004 | g0183 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01884 | hp2 | a0002 | c0002 | t0035 | g0343 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01891 | hp1 | a0004 | c0003 | t0010 | g0301 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01891 | hp2 | a0024 | c0027 | t0021 | g0197 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01943 | hp1 | a0010 | c0010 | t0025 | g0281 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01975 | hp1 | a0007 | c0008 | t0001 | g0078 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01975 | hp2 | a0006 | c0005 | t0030 | g0062 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01978 | hp1 | a0006 | c0005 | t0002 | g0164 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01978 | hp2 | a0006 | c0005 | t0024 | g0139 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01981 | hp1 | a0006 | c0005 | t0002 | g0106 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01981 | hp2 | a0012 | c0013 | t0005 | g0107 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01993 | hp1 | a0006 | c0005 | t0002 | g0013 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01993 | hp2 | a0006 | c0005 | t0002 | g0100 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02004 | hp1 | a0003 | c0004 | t0001 | g0117 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02004 | hp2 | a0012 | c0013 | t0005 | g0006 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02015 | hp1 | a0014 | c0014 | t0001 | g0115 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02015 | hp2 | a0007 | c0008 | t0001 | g0348 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02027 | hp1 | a0008 | c0007 | t0002 | g0319 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02027 | hp2 | a0003 | c0004 | t0001 | g0127 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02040 | hp1 | a0003 | c0004 | t0001 | g0170 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02040 | hp2 | a0008 | c0007 | t0002 | g0218 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02055 | hp1 | a0002 | c0024 | t0001 | g0283 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0252 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02071 | hp1 | a0004 | c0003 | t0004 | g0231 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02080 | hp1 | a0008 | c0039 | t0028 | g0012 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02080 | hp2 | a0015 | c0012 | t0012 | g0105 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02083 | hp1 | a0003 | c0004 | t0001 | g0124 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02129 | hp1 | a0003 | c0004 | t0001 | g0094 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02132 | hp1 | a0007 | c0008 | t0001 | g0357 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02132 | hp2 | a0014 | c0014 | t0003 | g0040 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02135 | hp2 | a0003 | c0004 | t0001 | g0059 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02145 | hp1 | a0005 | c0006 | t0009 | g0193 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02145 | hp2 | a0013 | c0019 | t0004 | g0355 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02148 | hp1 | a0012 | c0013 | t0005 | g0020 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02148 | hp2 | a0006 | c0005 | t0002 | g0043 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02155 | hp2 | a0004 | c0003 | t0004 | g0356 | EAS | CDX | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02165 | hp1 | a0003 | c0004 | t0001 | g0122 | EAS | CDX | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02165 | hp2 | a0004 | c0003 | t0027 | g0309 | EAS | CDX | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02257 | hp1 | a0002 | c0002 | t0003 | g0211 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02257 | hp2 | a0006 | c0005 | t0013 | g0173 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0207 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02258 | hp2 | a0011 | c0011 | t0005 | g0178 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02273 | hp1 | a0006 | c0005 | t0002 | g0099 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02273 | hp2 | a0006 | c0005 | t0002 | g0061 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02280 | hp1 | a0007 | c0008 | t0001 | g0016 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0208 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0292 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02300 | hp1 | a0003 | c0004 | t0001 | g0015 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02300 | hp2 | a0014 | c0014 | t0001 | g0072 | AMR | PEL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0217 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02451 | hp2 | a0016 | c0016 | t0002 | g0075 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02523 | hp1 | a0021 | c0021 | t0001 | g0039 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02523 | hp2 | a0003 | c0004 | t0001 | g0157 | EAS | KHV | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02572 | hp1 | a0013 | c0018 | t0004 | g0175 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02572 | hp2 | a0012 | c0042 | t0005 | g0176 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02615 | hp2 | a0013 | c0019 | t0004 | g0191 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02622 | hp1 | a0002 | c0002 | t0003 | g0212 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02630 | hp1 | a0003 | c0004 | t0003 | g0187 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02647 | hp1 | a0003 | c0004 | t0001 | g0093 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02683 | hp1 | a0006 | c0005 | t0002 | g0060 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02683 | hp2 | a0007 | c0008 | t0001 | g0051 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02698 | hp2 | a0005 | c0006 | t0001 | g0351 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02717 | hp1 | a0011 | c0011 | t0004 | g0182 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02717 | hp2 | a0022 | c0025 | t0015 | g0195 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02723 | hp1 | a0032 | c0035 | t0002 | g0254 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02723 | hp2 | a0005 | c0006 | t0003 | g0327 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02735 | hp1 | a0004 | c0003 | t0032 | g0200 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02735 | hp2 | a0012 | c0013 | t0005 | g0087 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0210 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02809 | hp2 | a0004 | c0003 | t0007 | g0248 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0198 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02818 | hp2 | a0005 | c0017 | t0005 | g0214 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0253 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02886 | hp2 | a0013 | c0019 | t0004 | g0190 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0255 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02896 | hp1 | a0013 | c0018 | t0004 | g0029 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02896 | hp2 | a0019 | c0022 | t0005 | g0244 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02897 | hp1 | a0013 | c0018 | t0004 | g0028 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02897 | hp2 | a0002 | c0002 | t0003 | g0256 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02922 | hp1 | a0011 | c0011 | t0004 | g0181 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02922 | hp2 | a0013 | c0018 | t0004 | g0188 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02965 | hp1 | a0005 | c0038 | t0003 | g0340 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02965 | hp2 | a0017 | c0020 | t0002 | g0322 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02970 | hp1 | a0019 | c0022 | t0005 | g0308 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02970 | hp2 | a0004 | c0003 | t0007 | g0354 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02976 | hp1 | a0004 | c0003 | t0010 | g0328 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02976 | hp2 | a0015 | c0012 | t0019 | g0350 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03017 | hp1 | a0004 | c0003 | t0008 | g0239 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03017 | hp2 | a0006 | c0005 | t0023 | g0071 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03041 | hp1 | a0004 | c0003 | t0004 | g0206 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03041 | hp2 | a0004 | c0003 | t0007 | g0257 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03098 | hp1 | a0005 | c0006 | t0009 | g0192 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03098 | hp2 | a0016 | c0016 | t0002 | g0108 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03130 | hp1 | a0001 | c0043 | t0001 | g0089 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03130 | hp2 | a0011 | c0011 | t0005 | g0177 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03139 | hp1 | a0004 | c0003 | t0010 | g0300 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03139 | hp2 | a0017 | c0020 | t0002 | g0359 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03195 | hp1 | a0013 | c0019 | t0004 | g0353 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03195 | hp2 | a0011 | c0011 | t0004 | g0184 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03209 | hp1 | a0017 | c0020 | t0002 | g0335 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03209 | hp2 | a0002 | c0002 | t0003 | g0185 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03225 | hp1 | a0005 | c0017 | t0005 | g0290 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0338 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03453 | hp1 | a0004 | c0003 | t0007 | g0249 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03453 | hp2 | a0005 | c0017 | t0005 | g0216 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03486 | hp1 | a0005 | c0017 | t0005 | g0215 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03486 | hp2 | a0015 | c0012 | t0007 | g0349 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03490 | hp1 | a0007 | c0015 | t0001 | g0046 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03490 | hp2 | a0012 | c0013 | t0005 | g0147 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03491 | hp1 | a0023 | c0028 | t0001 | g0002 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03491 | hp2 | a0004 | c0003 | t0008 | g0242 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03492 | hp1 | a0007 | c0015 | t0001 | g0045 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03492 | hp2 | a0023 | c0028 | t0001 | g0002 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03516 | hp2 | a0022 | c0025 | t0015 | g0204 | AFR | ESN | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03540 | hp1 | a0007 | c0008 | t0001 | g0017 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03540 | hp2 | a0006 | c0005 | t0013 | g0174 | AFR | GWD | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03579 | hp1 | a0016 | c0016 | t0002 | g0104 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03579 | hp2 | a0004 | c0003 | t0010 | g0299 | AFR | MSL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03654 | hp1 | a0007 | c0015 | t0001 | g0101 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03654 | hp2 | a0006 | c0005 | t0029 | g0007 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03669 | hp1 | a0018 | c0026 | t0016 | g0081 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03669 | hp2 | a0008 | c0007 | t0002 | g0334 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03704 | hp1 | a0003 | c0004 | t0001 | g0123 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03704 | hp2 | a0007 | c0015 | t0001 | g0189 | SAS | PJL | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03831 | hp1 | a0036 | c0047 | t0001 | g0304 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03831 | hp2 | a0004 | c0003 | t0008 | g0241 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03834 | hp1 | a0020 | c0023 | t0009 | g0136 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03834 | hp2 | a0018 | c0026 | t0016 | g0080 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03927 | hp1 | a0015 | c0012 | t0004 | g0152 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03927 | hp2 | a0008 | c0007 | t0002 | g0321 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03942 | hp1 | a0004 | c0003 | t0008 | g0238 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG03942 | hp2 | a0007 | c0008 | t0001 | g0325 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04184 | hp2 | a0020 | c0023 | t0037 | g0035 | SAS | BEB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04199 | hp1 | a0029 | c0037 | t0001 | g0306 | SAS | STU | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04199 | hp2 | a0007 | c0015 | t0001 | g0073 | SAS | STU | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04204 | hp1 | a0025 | c0029 | t0003 | g0282 | SAS | STU | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04228 | hp1 | a0001 | c0001 | t0034 | g0111 | SAS | STU | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG04228 | hp2 | a0012 | c0013 | t0005 | g0235 | SAS | STU | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18522 | hp1 | a0015 | c0012 | t0007 | g0085 | AFR | YRI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18522 | hp2 | a0004 | c0003 | t0007 | g0251 | AFR | YRI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18747 | hp1 | a0006 | c0005 | t0002 | g0148 | EAS | CHB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18747 | hp2 | a0021 | c0021 | t0001 | g0033 | EAS | CHB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0209 | AFR | YRI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18906 | hp2 | a0016 | c0016 | t0002 | g0145 | AFR | YRI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18940 | hp1 | a0034 | c0046 | t0002 | g0297 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18940 | hp2 | a0003 | c0004 | t0001 | g0167 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18941 | hp1 | a0003 | c0004 | t0001 | g0156 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18941 | hp2 | a0002 | c0002 | t0003 | g0302 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18942 | hp1 | a0004 | c0003 | t0004 | g0222 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18943 | hp1 | a0007 | c0008 | t0001 | g0303 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18943 | hp2 | a0003 | c0004 | t0001 | g0162 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18945 | hp1 | a0014 | c0014 | t0001 | g0083 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18945 | hp2 | a0009 | c0009 | t0006 | g0275 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18946 | hp1 | a0009 | c0009 | t0006 | g0269 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18946 | hp2 | a0008 | c0007 | t0002 | g0024 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18947 | hp1 | a0010 | c0010 | t0006 | g0264 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18947 | hp2 | a0001 | c0001 | t0017 | g0077 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18950 | hp1 | a0008 | c0007 | t0002 | g0314 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18950 | hp2 | a0009 | c0009 | t0006 | g0274 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18952 | hp1 | a0003 | c0004 | t0001 | g0113 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18952 | hp2 | a0010 | c0010 | t0006 | g0262 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18953 | hp2 | a0005 | c0006 | t0001 | g0329 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18957 | hp1 | a0005 | c0006 | t0001 | g0291 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18959 | hp1 | a0003 | c0004 | t0001 | g0125 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18959 | hp2 | a0008 | c0007 | t0002 | g0324 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18960 | hp2 | a0005 | c0006 | t0001 | g0312 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18962 | hp2 | a0010 | c0010 | t0006 | g0265 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18963 | hp1 | a0003 | c0004 | t0001 | g0138 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18963 | hp2 | a0007 | c0008 | t0001 | g0074 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18964 | hp1 | a0008 | c0007 | t0002 | g0320 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18967 | hp1 | a0004 | c0003 | t0004 | g0226 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18967 | hp2 | a0007 | c0008 | t0001 | g0284 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18968 | hp1 | a0010 | c0010 | t0006 | g0261 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0347 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18969 | hp2 | a0010 | c0010 | t0006 | g0260 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18970 | hp1 | a0004 | c0003 | t0004 | g0223 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18971 | hp2 | a0003 | c0004 | t0001 | g0224 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18973 | hp1 | a0015 | c0012 | t0006 | g0154 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18973 | hp2 | a0009 | c0009 | t0006 | g0272 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18974 | hp1 | a0004 | c0003 | t0004 | g0221 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18974 | hp2 | a0006 | c0005 | t0002 | g0070 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18975 | hp1 | a0006 | c0005 | t0002 | g0109 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18977 | hp1 | a0005 | c0006 | t0001 | g0339 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18978 | hp2 | a0003 | c0004 | t0001 | g0055 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18982 | hp1 | a0003 | c0004 | t0001 | g0054 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18982 | hp2 | a0004 | c0003 | t0004 | g0219 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18983 | hp1 | a0004 | c0003 | t0004 | g0220 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18983 | hp2 | a0009 | c0009 | t0006 | g0271 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18984 | hp1 | a0003 | c0004 | t0001 | g0166 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18984 | hp2 | a0004 | c0003 | t0004 | g0229 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18985 | hp1 | a0002 | c0002 | t0003 | g0323 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18985 | hp2 | a0008 | c0007 | t0002 | g0022 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18986 | hp1 | a0009 | c0009 | t0006 | g0273 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18986 | hp2 | a0005 | c0006 | t0001 | g0330 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18989 | hp1 | a0005 | c0006 | t0001 | g0311 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18989 | hp2 | a0004 | c0003 | t0004 | g0232 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18992 | hp1 | a0003 | c0004 | t0001 | g0119 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0336 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18994 | hp2 | a0014 | c0014 | t0001 | g0097 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18995 | hp1 | a0008 | c0007 | t0002 | g0023 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18995 | hp2 | a0026 | c0030 | t0006 | g0259 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18997 | hp1 | a0006 | c0005 | t0002 | g0153 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18997 | hp2 | a0010 | c0010 | t0006 | g0263 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18999 | hp1 | a0009 | c0009 | t0006 | g0270 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA18999 | hp2 | a0003 | c0004 | t0001 | g0038 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19000 | hp1 | a0003 | c0004 | t0001 | g0086 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19000 | hp2 | a0002 | c0002 | t0003 | g0298 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19001 | hp2 | a0004 | c0003 | t0004 | g0236 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19003 | hp2 | a0009 | c0009 | t0006 | g0268 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19004 | hp2 | a0008 | c0007 | t0002 | g0316 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19007 | hp1 | a0009 | c0009 | t0006 | g0277 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19007 | hp2 | a0006 | c0005 | t0002 | g0032 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19009 | hp1 | a0003 | c0004 | t0001 | g0120 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19009 | hp2 | a0009 | c0009 | t0006 | g0266 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19030 | hp1 | a0016 | c0016 | t0002 | g0168 | AFR | LWK | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19043 | hp1 | a0019 | c0022 | t0005 | g0196 | AFR | LWK | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19043 | hp2 | a0005 | c0006 | t0003 | g0358 | AFR | LWK | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19056 | hp2 | a0005 | c0006 | t0001 | g0310 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0134 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19057 | hp2 | a0035 | c0045 | t0022 | g0287 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19060 | hp1 | a0008 | c0007 | t0002 | g0318 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19066 | hp1 | a0009 | c0009 | t0006 | g0267 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19068 | hp2 | a0003 | c0004 | t0001 | g0063 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19078 | hp2 | a0002 | c0002 | t0033 | g0294 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19079 | hp1 | a0003 | c0004 | t0001 | g0036 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19079 | hp2 | a0002 | c0002 | t0003 | g0317 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19080 | hp1 | a0007 | c0008 | t0001 | g0296 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19080 | hp2 | a0003 | c0004 | t0003 | g0121 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19083 | hp1 | a0001 | c0001 | t0017 | g0161 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19083 | hp2 | a0003 | c0004 | t0001 | g0114 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19085 | hp2 | a0002 | c0033 | t0001 | g0342 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19086 | hp1 | a0009 | c0009 | t0006 | g0276 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19086 | hp2 | a0003 | c0004 | t0001 | g0128 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19088 | hp1 | a0033 | c0041 | t0001 | g0126 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19088 | hp2 | a0007 | c0008 | t0001 | g0293 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19090 | hp1 | a0008 | c0007 | t0002 | g0237 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19090 | hp2 | a0006 | c0005 | t0026 | g0041 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19091 | hp1 | a0005 | c0006 | t0001 | g0289 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19091 | hp2 | a0004 | c0003 | t0004 | g0230 | EAS | JPT | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19240 | hp1 | a0031 | c0036 | t0002 | g0225 | AFR | YRI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | ASW | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20129 | hp2 | a0017 | c0020 | t0002 | g0345 | AFR | ASW | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20752 | hp1 | a0004 | c0003 | t0012 | g0201 | EUR | TSI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | TSI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20905 | hp1 | a0004 | c0003 | t0008 | g0246 | SAS | GIH | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20905 | hp2 | a0008 | c0007 | t0002 | g0346 | SAS | GIH | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01123 | hp1 | a0004 | c0003 | t0004 | g0240 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02109 | hp1 | a0011 | c0011 | t0005 | g0179 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02109 | hp2 | a0007 | c0008 | t0001 | g0307 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02486 | hp1 | a0011 | c0011 | t0004 | g0247 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02486 | hp2 | a0005 | c0006 | t0001 | g0352 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02559 | hp1 | a0007 | c0008 | t0001 | g0018 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG02559 | hp2 | a0004 | c0003 | t0007 | g0250 | AFR | ACB | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG06807 | hp1 | a0006 | c0005 | t0013 | g0172 | AFR | USA | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| HG06807 | hp2 | a0002 | c0002 | t0036 | g0056 | AFR | USA | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20300 | hp1 | a0002 | c0002 | t0003 | g0213 | AFR | USA | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | USA | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA21309 | hp1 | a0018 | c0034 | t0005 | g0258 | AFR | LWK | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| NA21309 | hp2 | a0024 | c0027 | t0005 | g0180 | AFR | LWK | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0155 | REF | REF | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| homoSapiens_grch38 | hp1 | a0014 | c0014 | t0003 | g0194 | REF | REF | P2RX7_chr12_121127876_121193032 | P2RX7 | chr12 | 121127876 | 121193032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121154886
|
T | C | 4 | a0009a0010a0025others(1): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
missense_variant | MODERATE | c.227T>C | p.Val76Ala | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/13 | 322/5113 | 227/1788 | 76/595 | chr12 | 121154886 | ||
| chr12:121154912
|
C | T | 1 | a0036 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.253C>T | p.His85Tyr | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/13 | 348/5113 | 253/1788 | 85/595 | chr12 | 121154912 | ||
| chr12:121162430
|
A | G | 2 | a0034a0035 | 2 | NA18940.hp1 NA19057.hp2 |
missense_variant | MODERATE | c.443A>G | p.Gln148Arg | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/13 | 538/5113 | 443/1788 | 148/595 | chr12 | 121162430 | ||
| chr12:121162435
|
G | A | 1 | a0021 | 3 | HG01106.hp2 HG02523.hp1 NA18747.hp2 |
missense_variant | MODERATE | c.448G>A | p.Gly150Arg | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/13 | 543/5113 | 448/1788 | 150/595 | chr12 | 121162435 | ||
| chr12:121162450
|
T | C | 23 | a0002a0004a0005others(20): Show | 200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
missense_variant | MODERATE | c.463T>C | p.Tyr155His | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/13 | 558/5113 | 463/1788 | 155/595 | chr12 | 121162450 | ||
| chr12:121167551
|
C | T | 1 | a0017 | 4 | HG02965.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.808C>T | p.Arg270Cys | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/13 | 903/5113 | 808/1788 | 270/595 | chr12 | 121167551 | ||
| chr12:121167552
|
G | A | 7 | a0002a0003a0020others(4): Show | 92 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(89): Show |
missense_variant | MODERATE | c.809G>A | p.Arg270His | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/13 | 904/5113 | 809/1788 | 270/595 | chr12 | 121167552 | ||
| chr12:121167570
|
G | A | 2 | a0020a0027 | 4 | HG00323.hp2 HG01109.hp2 HG03834.hp1 others(1): Show |
missense_variant | MODERATE | c.827G>A | p.Arg276His | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/13 | 922/5113 | 827/1788 | 276/595 | chr12 | 121167570 | ||
| chr12:121175465
|
T | C | 2 | a0031a0032 | 2 | HG02723.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.959T>C | p.Leu320Pro | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/13 | 1054/5113 | 959/1788 | 320/595 | chr12 | 121175465 | ||
| chr12:121177300
|
G | A | 15 | a0004a0009a0010others(12): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
missense_variant | MODERATE | c.1042G>A | p.Ala348Thr | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/13 | 1137/5113 | 1042/1788 | 348/595 | chr12 | 121177300 | ||
| chr12:121177328
|
C | G | 7 | a0006a0008a0016others(4): Show | 55 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
missense_variant | MODERATE | c.1070C>G | p.Thr357Ser | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/13 | 1165/5113 | 1070/1788 | 357/595 | chr12 | 121177328 | ||
| chr12:121180432
|
G | A | 1 | a0009 | 12 | NA18945.hp2 NA18946.hp1 NA18950.hp2 others(9): Show |
missense_variant | MODERATE | c.1267G>A | p.Asp423Asn | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/13 | 1362/5113 | 1267/1788 | 423/595 | chr12 | 121180432 | ||
| chr12:121180454
|
C | G | 2 | a0013a0030 | 9 | HG01243.hp2 HG02145.hp2 HG02572.hp1 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.1289C>G | p.Pro430Arg | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/13 | 1384/5113 | 1289/1788 | 430/595 | chr12 | 121180454 | ||
| chr12:121184312
|
C | T | 2 | a0011a0019 | 13 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
missense_variant | MODERATE | c.1298C>T | p.Ala433Val | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1393/5113 | 1298/1788 | 433/595 | chr12 | 121184312 | ||
| chr12:121184393
|
A | G | 3 | a0012a0018a0030 | 13 | HG01069.hp2 HG01243.hp2 HG01517.hp2 others(10): Show |
missense_variant | MODERATE | c.1379A>G | p.Gln460Arg | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1474/5113 | 1379/1788 | 460/595 | chr12 | 121184393 | ||
| chr12:121184501
|
A | C | 5 | a0001a0007a0021others(2): Show | 78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
missense_variant | MODERATE | c.1487A>C | p.Glu496Ala | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1582/5113 | 1487/1788 | 496/595 | chr12 | 121184501 | ||
| chr12:121184534
|
T | C | 1 | a0023 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.1520T>C | p.Ile507Thr | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1615/5113 | 1520/1788 | 507/595 | chr12 | 121184534 | ||
| chr12:121184577
|
C | G | 4 | a0011a0019a0022others(1): Show | 17 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
missense_variant | MODERATE | c.1563C>G | p.His521Gln | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1658/5113 | 1563/1788 | 521/595 | chr12 | 121184577 | ||
| chr12:121184578
|
G | A | 1 | a0016 | 5 | HG02451.hp2 HG03098.hp2 HG03579.hp1 others(2): Show |
missense_variant | MODERATE | c.1564G>A | p.Val522Ile | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1659/5113 | 1564/1788 | 522/595 | chr12 | 121184578 | ||
| chr12:121184605
|
G | T | 1 | a0026 | 1 | NA18995.hp2 | stop_gained | HIGH | c.1591G>T | p.Glu531* | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1686/5113 | 1591/1788 | 531/595 | chr12 | 121184605 | ||
| chr12:121184717
|
T | A | 1 | a0028 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.1703T>A | p.Ile568Asn | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1798/5113 | 1703/1788 | 568/595 | chr12 | 121184717 | ||
| chr12:121184758
|
C | T | 1 | a0033 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.1744C>T | p.Pro582Ser | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1839/5113 | 1744/1788 | 582/595 | chr12 | 121184758 | ||
| chr12:121184759
|
C | T | 1 | a0031 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1745C>T | p.Pro582Leu | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1840/5113 | 1745/1788 | 582/595 | chr12 | 121184759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121154893
|
T | C | 1 | a0005c0017 | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.234T>C | p.Asn78Asn | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/13 | 329/5113 | 234/1788 | 78/595 | chr12 | 121154893 | ||
| chr12:121162434
|
C | T | 1 | a0003c0044 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.447C>T | p.Thr149Thr | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/13 | 542/5113 | 447/1788 | 149/595 | chr12 | 121162434 | ||
| chr12:121162449
|
G | A | 4 | a0002c0024a0007c0015a0013c0018others(1): Show | 12 | HG01243.hp2 HG01358.hp2 HG02055.hp1 others(9): Show |
synonymous_variant | LOW | c.462G>A | p.Val154Val | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/13 | 557/5113 | 462/1788 | 154/595 | chr12 | 121162449 | ||
| chr12:121162491
|
C | T | 1 | a0028c0040 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.504C>T | p.Cys168Cys | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/13 | 599/5113 | 504/1788 | 168/595 | chr12 | 121162491 | ||
| chr12:121175397
|
G | A | 2 | a0012c0042a0018c0034 | 2 | HG02572.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.891G>A | p.Lys297Lys | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/13 | 986/5113 | 891/1788 | 297/595 | chr12 | 121175397 | ||
| chr12:121184436
|
C | T | 7 | a0006c0005a0008c0007a0016c0016others(4): Show | 54 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(51): Show |
synonymous_variant | LOW | c.1422C>T | p.Pro474Pro | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1517/5113 | 1422/1788 | 474/595 | chr12 | 121184436 | ||
| chr12:121184523
|
G | A | 1 | a0005c0038 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1509G>A | p.Pro503Pro | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1604/5113 | 1509/1788 | 503/595 | chr12 | 121184523 | ||
| chr12:121184616
|
G | T | 9 | a0002c0033a0006c0005a0008c0007others(6): Show | 56 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(53): Show |
synonymous_variant | LOW | c.1602G>T | p.Leu534Leu | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1697/5113 | 1602/1788 | 534/595 | chr12 | 121184616 | ||
| chr12:121184619
|
G | A | 1 | a0001c0043 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1605G>A | p.Ala535Ala | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1700/5113 | 1605/1788 | 535/595 | chr12 | 121184619 | ||
| chr12:121184760
|
G | A | 17 | a0004c0003a0009c0009a0010c0010others(14): Show | 109 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(106): Show |
synonymous_variant | LOW | c.1746G>A | p.Pro582Pro | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1841/5113 | 1746/1788 | 582/595 | chr12 | 121184760 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121184838
|
G | A | 1 | a0006c0005t0018 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 36 | chr12 | 121184838 | |||||
| chr12:121184872
|
G | A | 5 | a0004c0003t0007a0004c0003t0010a0004c0003t0020others(2): Show | 14 | HG01243.hp1 HG01891.hp1 HG02559.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*70G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 70 | chr12 | 121184872 | |||||
| chr12:121185078
|
TC | T | 4 | a0004c0003t0012a0004c0003t0031a0004c0003t0032others(1): Show | 6 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*281delC | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 281 | INFO_REALIGN_3_PRIME | chr12 | 121185078 | ||||
| chr12:121185081
|
C | CA | 4 | a0004c0003t0008a0004c0003t0011a0010c0010t0011others(1): Show | 11 | HG01074.hp2 HG01168.hp1 HG01255.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*279_*280insA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 280 | chr12 | 121185081 | |||||
| chr12:121185082
|
C | A | 47 | a0004c0003t0004a0004c0003t0007a0004c0003t0008others(44): Show | 162 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 280 | chr12 | 121185082 | |||||
| chr12:121185083
|
C | A | 71 | a0001c0001t0001a0001c0001t0017a0001c0001t0034others(68): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
3_prime_UTR_variant | MODIFIER | c.*281C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 281 | chr12 | 121185083 | |||||
| chr12:121185084
|
A | C | 4 | a0005c0006t0009a0020c0023t0009a0020c0023t0037others(1): Show | 6 | HG00323.hp2 HG01109.hp2 HG02145.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*282A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 282 | chr12 | 121185084 | |||||
| chr12:121185746
|
A | C | 1 | a0006c0005t0030 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 944 | chr12 | 121185746 | |||||
| chr12:121185830
|
C | T | 1 | a0015c0012t0014 | 2 | HG01255.hp1 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1028C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1028 | chr12 | 121185830 | |||||
| chr12:121186053
|
C | CA | 8 | a0004c0003t0010a0004c0003t0012a0004c0003t0020others(5): Show | 14 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1265dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1266 | INFO_REALIGN_3_PRIME | chr12 | 121186053 | ||||
| chr12:121186053
|
C | CAA | 2 | a0004c0003t0007a0015c0012t0007 | 8 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1264_*1265dupAA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1266 | INFO_REALIGN_3_PRIME | chr12 | 121186053 | ||||
| chr12:121186100
|
C | T | 1 | a0006c0005t0029 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1298C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1298 | chr12 | 121186100 | |||||
| chr12:121186118
|
C | T | 1 | a0020c0023t0037 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1316C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1316 | chr12 | 121186118 | |||||
| chr12:121186186
|
T | C | 1 | a0035c0045t0022 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1384T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1384 | chr12 | 121186186 | |||||
| chr12:121186305
|
C | G | 10 | a0002c0002t0035a0004c0003t0004a0004c0003t0011others(7): Show | 38 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1503C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1503 | chr12 | 121186305 | |||||
| chr12:121186419
|
G | A | 1 | a0001c0001t0017 | 2 | NA18947.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1617G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1617 | chr12 | 121186419 | |||||
| chr12:121186422
|
G | T | 1 | a0004c0003t0020 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1620 | chr12 | 121186422 | |||||
| chr12:121186506
|
C | T | 3 | a0004c0003t0012a0004c0003t0031a0015c0012t0012 | 5 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1704C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1704 | chr12 | 121186506 | |||||
| chr12:121186552
|
A | G | 3 | a0004c0003t0007a0015c0012t0007a0015c0012t0019 | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1750A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1750 | chr12 | 121186552 | |||||
| chr12:121186608
|
G | A | 1 | a0006c0005t0023 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1806G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1806 | chr12 | 121186608 | |||||
| chr12:121186641
|
G | A | 1 | a0006c0005t0024 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1839G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1839 | chr12 | 121186641 | |||||
| chr12:121186742
|
C | T | 1 | a0004c0003t0027 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1940C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 1940 | chr12 | 121186742 | |||||
| chr12:121186865
|
G | T | 1 | a0002c0002t0036 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2063G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2063 | chr12 | 121186865 | |||||
| chr12:121187151
|
T | C | 1 | a0018c0026t0016 | 2 | HG03669.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2349T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2349 | chr12 | 121187151 | |||||
| chr12:121187288
|
G | A | 35 | a0002c0002t0035a0004c0003t0004a0004c0003t0007others(32): Show | 112 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2486G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2486 | chr12 | 121187288 | |||||
| chr12:121187405
|
A | G | 1 | a0022c0025t0015 | 2 | HG02717.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2603A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2603 | chr12 | 121187405 | |||||
| chr12:121187457
|
C | T | 1 | a0004c0003t0031 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2655C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2655 | chr12 | 121187457 | |||||
| chr12:121187507
|
T | C | 5 | a0009c0009t0006a0010c0010t0006a0015c0012t0006others(2): Show | 21 | NA18945.hp2 NA18946.hp1 NA18947.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2705T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2705 | chr12 | 121187507 | |||||
| chr12:121187511
|
A | G | 1 | a0001c0001t0034 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2709A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2709 | chr12 | 121187511 | |||||
| chr12:121187645
|
TG | T | 3 | a0004c0003t0008a0004c0003t0027a0010c0010t0025 | 7 | HG01943.hp1 HG02165.hp2 HG03017.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2846delG | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2846 | INFO_REALIGN_3_PRIME | chr12 | 121187645 | ||||
| chr12:121187712
|
G | A | 2 | a0002c0002t0033a0006c0005t0013 | 4 | HG02257.hp2 HG03540.hp2 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2910G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 2910 | chr12 | 121187712 | |||||
| chr12:121187825
|
C | T | 1 | a0006c0005t0026 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3023C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 13/13 | 3023 | chr12 | 121187825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:121133096
|
G | T | 2 | a0001c0001t0001g0360a0003c0004t0001g0361 | 2 | HG01167.hp2 HG01169.hp2 |
splice_donor_variant&intron_variant | HIGH | c.125+1G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133096 | ||||||
| chr12:121133341
|
G | A | 1 | a0012c0013t0005g0006 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.125+246G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133341 | ||||||
| chr12:121133360
|
T | C | 1 | a0006c0005t0029g0007 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.125+265T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133360 | ||||||
| chr12:121133418
|
C | T | 76 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(73): Show | 76 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.125+323C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133418 | ||||||
| chr12:121133424
|
G | T | 1 | a0002c0024t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.125+329G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133424 | ||||||
| chr12:121133662
|
C | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.125+567C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133662 | ||||||
| chr12:121133843
|
C | T | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+748C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133843 | ||||||
| chr12:121133893
|
AT | A | 79 | a0001c0001t0001g0008a0001c0001t0001g0331a0002c0002t0001g0285others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.125+809delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121133893 | |||||
| chr12:121133976
|
G | A | 76 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(73): Show | 76 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.125+881G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121133976 | ||||||
| chr12:121134019
|
C | T | 1 | a0018c0034t0005g0258 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.125+924C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134019 | ||||||
| chr12:121134164
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.125+1069T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134164 | ||||||
| chr12:121134333
|
A | G | 10 | a0002c0002t0003g0252a0002c0002t0003g0253a0002c0002t0003g0255others(7): Show | 10 | HG02055.hp2 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+1238A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134333 | ||||||
| chr12:121134354
|
C | T | 1 | a0011c0011t0004g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125+1259C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134354 | ||||||
| chr12:121134494
|
C | T | 1 | a0004c0003t0008g0246 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.125+1399C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134494 | ||||||
| chr12:121134542
|
T | C | 15 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.125+1447T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134542 | ||||||
| chr12:121134609
|
C | T | 1 | a0017c0020t0002g0359 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+1514C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134609 | ||||||
| chr12:121134634
|
C | T | 1 | a0005c0006t0003g0358 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.125+1539C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134634 | ||||||
| chr12:121134783
|
CT | C | 9 | a0002c0002t0003g0185a0002c0024t0003g0186a0003c0004t0003g0187others(6): Show | 9 | HG01358.hp2 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.125+1689delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134783 | ||||||
| chr12:121134820
|
G | C | 1 | a0008c0039t0028g0012 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.125+1725G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121134820 | ||||||
| chr12:121135106
|
C | T | 17 | a0004c0003t0020g0245a0006c0005t0013g0172a0006c0005t0013g0173others(14): Show | 18 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.125+2011C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135106 | ||||||
| chr12:121135107
|
A | G | 350 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(347): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.125+2012A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135107 | ||||||
| chr12:121135264
|
G | A | 2 | a0001c0001t0001g0014a0006c0005t0002g0013 | 2 | HG01346.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.125+2169G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135264 | ||||||
| chr12:121135287
|
A | G | 350 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(347): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.125+2192A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135287 | ||||||
| chr12:121135818
|
C | T | 28 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(25): Show | 28 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.125+2723C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135818 | ||||||
| chr12:121135819
|
G | A | 1 | a0003c0004t0001g0015 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.125+2724G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135819 | ||||||
| chr12:121135833
|
A | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(177): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.125+2738A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135833 | ||||||
| chr12:121135883
|
A | G | 2 | a0004c0003t0004g0356a0007c0008t0001g0357 | 2 | HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.125+2788A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121135883 | ||||||
| chr12:121136003
|
C | CAAA | 19 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(16): Show | 19 | NA18945.hp2 NA18946.hp1 NA18947.hp1 others(16): Show |
intron_variant | MODIFIER | c.125+2927_125+2929d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136003 | |||||
| chr12:121136003
|
CA | C | 28 | a0002c0002t0003g0252a0002c0002t0003g0253a0002c0002t0003g0255others(25): Show | 29 | HG01099.hp1 HG01109.hp1 HG01358.hp2 others(26): Show |
intron_variant | MODIFIER | c.125+2929delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136003 | |||||
| chr12:121136017
|
A | ATATATAT others(18): Show |
1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.125+2922_125+2923i others(27): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136017 | ||||||
| chr12:121136019
|
A | ATATATAT others(16): Show |
1 | a0004c0003t0012g0205 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.125+2924_125+2925i others(25): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136019 | ||||||
| chr12:121136019
|
A | T | 2 | a0004c0003t0004g0206a0004c0003t0020g0245 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.125+2924A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136019 | ||||||
| chr12:121136021
|
A | AAT | 6 | a0003c0004t0001g0224a0004c0003t0004g0220a0004c0003t0004g0221others(3): Show | 6 | NA18942.hp1 NA18970.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+2927_125+2928i others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136021 | |||||
| chr12:121136021
|
A | ATAT | 11 | a0002c0002t0001g0227a0002c0002t0001g0228a0004c0003t0004g0226others(8): Show | 11 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+2926_125+2927i others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136021 | ||||||
| chr12:121136021
|
A | ATATAT | 5 | a0004c0003t0004g0240a0004c0003t0008g0238a0004c0003t0008g0239others(2): Show | 5 | HG01123.hp1 HG03017.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.125+2926_125+2927i others(7): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136021 | ||||||
| chr12:121136021
|
A | ATATATAT others(24): Show |
1 | a0004c0003t0031g0203 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125+2926_125+2927i others(33): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136021 | ||||||
| chr12:121136021
|
A | T | 19 | a0002c0002t0001g0243a0004c0003t0004g0206a0004c0003t0008g0241others(16): Show | 20 | HG00735.hp2 HG01099.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.125+2926A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136021 | ||||||
| chr12:121136023
|
A | AAAAAAAA others(25): Show |
1 | a0007c0008t0001g0284 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(34): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(27): Show |
1 | a0002c0002t0001g0285 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(36): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0019 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(23): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(26): Show |
1 | a0002c0002t0001g0286 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(35): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(30): Show |
1 | a0035c0045t0022g0287 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(39): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0021a0012c0013t0005g0020 | 2 | HG02148.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(24): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(17): Show |
2 | a0008c0007t0002g0022a0008c0007t0002g0023 | 2 | NA18985.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(26): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(16): Show |
2 | a0002c0002t0001g0025a0008c0007t0002g0024 | 2 | NA18946.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(25): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(26): Show |
2 | a0005c0006t0001g0289a0008c0007t0002g0288 | 2 | HG00438.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(35): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(9): Show |
1 | a0003c0004t0001g0026 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(18): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(15): Show |
4 | a0001c0001t0001g0027a0001c0001t0001g0030a0013c0018t0004g0028others(1): Show | 4 | HG00423.hp1 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(24): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0008 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(26): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(23): Show |
1 | a0005c0017t0005g0290 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(32): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(25): Show |
1 | a0005c0006t0001g0291 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(34): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(27): Show |
3 | a0002c0002t0001g0292a0002c0002t0033g0294a0007c0008t0001g0293 | 3 | HG02293.hp2 NA19078.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(36): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(29): Show |
2 | a0002c0002t0001g0295a0007c0008t0001g0296 | 2 | HG03516.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(38): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(31): Show |
1 | a0034c0046t0002g0297 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(40): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(14): Show |
4 | a0006c0005t0002g0032a0012c0013t0005g0009a0015c0012t0014g0031others(1): Show | 4 | HG01069.hp2 HG01255.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(23): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(16): Show |
2 | a0001c0001t0001g0034a0020c0023t0037g0035 | 2 | HG02895.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(25): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(24): Show |
5 | a0002c0002t0003g0298a0002c0002t0003g0302a0004c0003t0010g0299others(2): Show | 5 | HG01891.hp1 HG03139.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(33): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(26): Show |
2 | a0007c0008t0001g0303a0036c0047t0001g0304 | 2 | HG03831.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(35): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(28): Show |
4 | a0004c0003t0004g0356a0005c0006t0003g0358a0008c0007t0002g0305others(1): Show | 4 | HG00621.hp2 HG02155.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(37): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(32): Show |
2 | a0007c0008t0001g0307a0019c0022t0005g0308 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(41): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(34): Show |
1 | a0007c0008t0001g0357 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(43): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(11): Show |
1 | a0003c0004t0001g0036 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(20): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(13): Show |
4 | a0003c0004t0001g0038a0014c0014t0003g0040a0021c0021t0001g0039others(1): Show | 4 | HG01109.hp2 HG02132.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(22): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(15): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0047a0006c0005t0002g0043others(4): Show | 7 | HG01346.hp2 HG02148.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(24): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(17): Show |
1 | a0006c0005t0018g0048 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(26): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(23): Show |
1 | a0004c0003t0027g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(32): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(25): Show |
4 | a0002c0002t0001g0313a0005c0006t0001g0310a0005c0006t0001g0311others(1): Show | 4 | NA18960.hp2 NA18975.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(34): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(27): Show |
2 | a0002c0002t0001g0315a0008c0007t0002g0314 | 2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(36): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(29): Show |
2 | a0002c0002t0003g0317a0008c0007t0002g0316 | 2 | NA19004.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(38): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(31): Show |
2 | a0008c0007t0002g0318a0008c0007t0002g0319 | 2 | HG02027.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(40): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(35): Show |
1 | a0008c0007t0002g0320 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(44): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(39): Show |
1 | a0008c0007t0002g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(48): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(8): Show |
6 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(3): Show | 6 | HG01071.hp2 HG01361.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(17): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(10): Show |
2 | a0007c0008t0001g0051a0022c0025t0015g0195 | 2 | HG02683.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(19): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(12): Show |
5 | a0001c0001t0001g0052a0002c0002t0036g0056a0003c0004t0001g0054others(2): Show | 5 | HG01257.hp1 HG06807.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(21): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(14): Show |
14 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0001g0058others(11): Show | 14 | HG00280.hp2 HG01106.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(23): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(16): Show |
7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069others(4): Show | 7 | HG01167.hp1 HG02300.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(25): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(18): Show |
3 | a0001c0001t0001g0076a0007c0008t0001g0074a0016c0016t0002g0075 | 3 | HG02451.hp2 NA18963.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(27): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(20): Show |
1 | a0008c0039t0028g0012 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(29): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(24): Show |
1 | a0017c0020t0002g0322 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(33): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(26): Show |
4 | a0002c0002t0003g0323a0007c0008t0001g0325a0008c0007t0002g0324others(1): Show | 4 | HG00741.hp2 HG03942.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(35): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(28): Show |
2 | a0004c0003t0010g0328a0005c0006t0003g0327 | 2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(37): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(7): Show |
3 | a0002c0002t0003g0210a0002c0002t0003g0211a0002c0002t0003g0212 | 3 | HG02257.hp1 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(16): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0017g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(18): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(11): Show |
9 | a0002c0002t0001g0079a0003c0004t0001g0084a0005c0006t0001g0001others(6): Show | 10 | HG00558.hp2 HG00735.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(20): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(13): Show |
12 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0091others(9): Show | 12 | HG00099.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(22): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(15): Show |
10 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0102others(7): Show | 11 | HG01993.hp2 HG02071.hp2 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(24): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(17): Show |
7 | a0001c0001t0001g0011a0001c0001t0001g0110a0006c0005t0002g0106others(4): Show | 7 | HG01981.hp1 HG01981.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(26): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0034g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(28): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(25): Show |
4 | a0001c0001t0001g0331a0005c0006t0001g0329a0005c0006t0001g0330others(1): Show | 4 | HG00140.hp1 HG00323.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(34): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(27): Show |
1 | a0002c0002t0001g0333 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(36): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(29): Show |
2 | a0008c0007t0002g0334a0017c0020t0002g0335 | 2 | HG03209.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(38): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(33): Show |
1 | a0002c0002t0003g0336 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(42): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0112a0003c0004t0001g0003a0003c0004t0001g0113others(2): Show | 6 | HG01256.hp1 HG01258.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(17): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(10): Show |
3 | a0007c0008t0001g0010a0007c0008t0001g0116a0019c0022t0005g0196 | 3 | HG01069.hp1 HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(19): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(12): Show |
19 | a0001c0001t0001g0004a0001c0001t0001g0132a0002c0002t0001g0118others(16): Show | 20 | HG00140.hp2 HG01074.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(21): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(14): Show |
18 | a0001c0001t0001g0135a0001c0001t0001g0140a0001c0001t0001g0141others(15): Show | 18 | HG01099.hp2 HG01123.hp2 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(23): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(16): Show |
1 | a0006c0005t0002g0153 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(25): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(18): Show |
2 | a0001c0001t0001g0155a0015c0012t0006g0154 | 2 | NA18973.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(27): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(22): Show |
1 | a0005c0006t0001g0337 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(31): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(24): Show |
1 | a0002c0002t0003g0338 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(33): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(26): Show |
2 | a0005c0006t0001g0339a0005c0038t0003g0340 | 2 | HG02965.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(35): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(7): Show |
1 | a0003c0004t0001g0156 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(16): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(9): Show |
2 | a0007c0008t0001g0016a0007c0008t0001g0017 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(18): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(11): Show |
4 | a0001c0001t0001g0158a0001c0001t0001g0159a0003c0004t0001g0157others(1): Show | 4 | HG02523.hp2 HG02559.hp1 NA20805.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(20): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(13): Show |
4 | a0001c0001t0017g0161a0003c0004t0001g0162a0003c0004t0001g0163others(1): Show | 4 | HG00323.hp2 HG00438.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(22): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(15): Show |
1 | a0006c0005t0002g0164 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(24): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0165 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(28): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(21): Show |
1 | a0005c0006t0001g0341 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(30): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(25): Show |
1 | a0002c0033t0001g0342 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(34): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(27): Show |
5 | a0002c0002t0001g0344a0002c0002t0003g0347a0002c0002t0035g0343others(2): Show | 5 | HG01884.hp2 NA18969.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.125+2929_125+2930i others(36): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(27): Show |
1 | a0007c0008t0001g0348 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(36): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(8): Show |
1 | a0002c0002t0003g0213 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(17): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(12): Show |
2 | a0003c0004t0001g0166a0003c0004t0001g0167 | 2 | NA18940.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(21): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0169a0016c0016t0002g0168 | 2 | HG02293.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(23): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(22): Show |
1 | a0015c0012t0007g0349 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(31): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(7): Show |
1 | a0002c0002t0003g0217 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(16): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(11): Show |
1 | a0003c0004t0001g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.125+2929_125+2930i others(20): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(21): Show |
1 | a0015c0012t0019g0350 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(30): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAAAA others(27): Show |
2 | a0005c0006t0001g0351a0017c0020t0002g0359 | 2 | HG02698.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(36): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAATA others(7): Show |
1 | a0002c0002t0001g0171 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(16): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | AAAAAATA others(19): Show |
1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.125+2929_125+2930i others(28): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136023 | |||||
| chr12:121136023
|
A | ATATATAT others(16): Show |
1 | a0004c0003t0012g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.125+2928_125+2929i others(25): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136023 | ||||||
| chr12:121136023
|
A | ATATATAT others(18): Show |
1 | a0004c0003t0032g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.125+2928_125+2929i others(27): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136023 | ||||||
| chr12:121136023
|
A | ATATATAT others(20): Show |
1 | a0004c0003t0012g0201 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.125+2928_125+2929i others(29): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136023 | ||||||
| chr12:121136023
|
A | T | 54 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(51): Show | 55 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.125+2928A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136023 | ||||||
| chr12:121136024
|
A | AAAAAAAA others(8): Show |
3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.125+2929_125+2930i others(17): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136024 | ||||||
| chr12:121136061
|
G | A | 1 | a0004c0003t0007g0251 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.125+2966G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136061 | ||||||
| chr12:121136103
|
TTATATAT others(3): Show |
T | 1 | a0002c0002t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.125+3022_125+3031d others(12): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136103 | |||||
| chr12:121136194
|
T | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(177): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.125+3099T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136194 | ||||||
| chr12:121136286
|
A | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(165): Show | 172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.125+3191A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136286 | ||||||
| chr12:121136438
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.125+3343C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136438 | ||||||
| chr12:121136492
|
A | AT | 27 | a0002c0002t0003g0185a0002c0002t0003g0213a0002c0024t0003g0186others(24): Show | 28 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.125+3406dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136492 | |||||
| chr12:121136532
|
G | A | 8 | a0002c0002t0003g0338a0002c0002t0035g0343a0005c0006t0001g0337others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+3437G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136532 | ||||||
| chr12:121136607
|
C | T | 23 | a0004c0003t0004g0206a0009c0009t0006g0266a0009c0009t0006g0267others(20): Show | 23 | HG01074.hp2 HG01943.hp1 HG03041.hp1 others(20): Show |
intron_variant | MODIFIER | c.125+3512C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136607 | ||||||
| chr12:121136631
|
T | C | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0135 | 3 | HG02155.hp1 NA18977.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.125+3536T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136631 | ||||||
| chr12:121136647
|
C | CT | 55 | a0001c0001t0001g0052a0001c0001t0001g0095a0001c0001t0001g0331others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.125+3570dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136647 | |||||
| chr12:121136647
|
CT | C | 73 | a0001c0001t0001g0034a0001c0001t0001g0067a0001c0001t0001g0360others(70): Show | 74 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.125+3570delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136647 | |||||
| chr12:121136649
|
T | TTC | 19 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(16): Show | 19 | NA18945.hp2 NA18946.hp1 NA18947.hp1 others(16): Show |
intron_variant | MODIFIER | c.125+3555_125+3556i others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121136649 | |||||
| chr12:121136651
|
T | C | 1 | a0020c0023t0009g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.125+3556T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136651 | ||||||
| chr12:121136669
|
T | A | 12 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+3574T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136669 | ||||||
| chr12:121136699
|
T | C | 1 | a0035c0045t0022g0287 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.125+3604T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136699 | ||||||
| chr12:121136771
|
C | T | 11 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+3676C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121136771 | ||||||
| chr12:121137102
|
G | C | 3 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174 | 3 | HG02257.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.125+4007G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121137102 | ||||||
| chr12:121137179
|
G | A | 3 | a0018c0034t0005g0258a0024c0027t0021g0197a0030c0031t0002g0202 | 3 | HG01243.hp2 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125+4084G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121137179 | ||||||
| chr12:121137801
|
C | T | 2 | a0002c0002t0003g0198a0031c0036t0002g0225 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.125+4706C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121137801 | ||||||
| chr12:121137902
|
G | A | 10 | a0002c0002t0001g0313a0002c0002t0001g0315a0002c0002t0001g0333others(7): Show | 10 | HG00621.hp2 NA18950.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.125+4807G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121137902 | ||||||
| chr12:121138121
|
G | A | 337 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.125+5026G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138121 | ||||||
| chr12:121138122
|
C | T | 3 | a0001c0001t0001g0331a0008c0007t0002g0326a0008c0007t0002g0332 | 3 | HG00140.hp1 HG00323.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.125+5027C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138122 | ||||||
| chr12:121138184
|
G | A | 13 | a0004c0003t0004g0206a0004c0003t0012g0199a0004c0003t0012g0201others(10): Show | 13 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.125+5089G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138184 | ||||||
| chr12:121138237
|
C | T | 1 | a0003c0004t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.125+5142C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138237 | ||||||
| chr12:121138248
|
C | T | 1 | a0015c0012t0004g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.125+5153C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138248 | ||||||
| chr12:121138498
|
C | G | 1 | a0003c0004t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.125+5403C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138498 | ||||||
| chr12:121138499
|
T | C | 1 | a0003c0004t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.125+5404T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138499 | ||||||
| chr12:121138500
|
C | T | 1 | a0003c0004t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.125+5405C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138500 | ||||||
| chr12:121138543
|
C | A | 1 | a0017c0020t0002g0345 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.125+5448C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138543 | ||||||
| chr12:121138547
|
C | G | 1 | a0002c0002t0003g0212 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.125+5452C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138547 | ||||||
| chr12:121138641
|
G | A | 11 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.125+5546G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138641 | ||||||
| chr12:121138783
|
C | T | 1 | a0004c0003t0027g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.125+5688C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138783 | ||||||
| chr12:121138849
|
C | A | 179 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(176): Show | 183 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.125+5754C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121138849 | ||||||
| chr12:121139081
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.125+5986A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139081 | ||||||
| chr12:121139090
|
T | C | 17 | a0004c0003t0020g0245a0006c0005t0013g0172a0006c0005t0013g0173others(14): Show | 18 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.125+5995T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139090 | ||||||
| chr12:121139115
|
T | G | 2 | a0002c0002t0003g0198a0031c0036t0002g0225 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.125+6020T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139115 | ||||||
| chr12:121139189
|
G | C | 64 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(61): Show | 65 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.125+6094G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139189 | ||||||
| chr12:121139193
|
C | T | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125+6098C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139193 | ||||||
| chr12:121139415
|
C | T | 20 | a0002c0002t0001g0286a0002c0002t0001g0292a0002c0002t0003g0298others(17): Show | 20 | HG00423.hp2 HG02293.hp2 NA18941.hp2 others(17): Show |
intron_variant | MODIFIER | c.125+6320C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139415 | ||||||
| chr12:121139481
|
T | C | 75 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.125+6386T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139481 | ||||||
| chr12:121139733
|
C | CT | 157 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0014others(154): Show | 161 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.125+6657dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139733
|
C | CTT | 61 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0067others(58): Show | 62 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.125+6656_125+6657d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139733
|
C | CTTTTTT | 9 | a0002c0002t0003g0253a0002c0002t0003g0255a0002c0002t0003g0256others(6): Show | 9 | HG02559.hp2 HG02723.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.125+6652_125+6657d others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139733
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.125+6648_125+6657d others(12): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139733
|
CT | C | 11 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.125+6657delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139733
|
CTTT | C | 7 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+6655_125+6657d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139733
|
CTTTT | C | 25 | a0007c0008t0001g0284a0009c0009t0006g0266a0009c0009t0006g0267others(22): Show | 25 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.125+6654_125+6657d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139733
|
CTTTTT | C | 73 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(70): Show | 73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.125+6653_125+6657d others(7): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121139733 | |||||
| chr12:121139809
|
A | G | 59 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(56): Show | 60 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.125+6714A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139809 | ||||||
| chr12:121139831
|
T | C | 11 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.125+6736T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139831 | ||||||
| chr12:121139900
|
G | T | 4 | a0018c0034t0005g0258a0024c0027t0021g0197a0030c0031t0002g0202others(1): Show | 4 | HG01243.hp2 HG01891.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.125+6805G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139900 | ||||||
| chr12:121139975
|
G | A | 192 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.125+6880G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121139975 | ||||||
| chr12:121140044
|
T | C | 65 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(62): Show | 66 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.125+6949T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140044 | ||||||
| chr12:121140089
|
C | T | 74 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(71): Show | 75 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.125+6994C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140089 | ||||||
| chr12:121140148
|
G | A | 10 | a0002c0002t0003g0252a0002c0002t0003g0253a0002c0002t0003g0255others(7): Show | 10 | HG02055.hp2 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.125+7053G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140148 | ||||||
| chr12:121140184
|
T | C | 74 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(71): Show | 75 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.125+7089T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140184 | ||||||
| chr12:121140230
|
CAA | C | 64 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(61): Show | 65 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.125+7136_125+7137d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140230 | ||||||
| chr12:121140248
|
C | A | 1 | a0006c0005t0026g0041 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.125+7153C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140248 | ||||||
| chr12:121140318
|
C | T | 1 | a0002c0002t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.125+7223C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140318 | ||||||
| chr12:121140353
|
A | G | 1 | a0002c0002t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.125+7258A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140353 | ||||||
| chr12:121140529
|
G | A | 1 | a0028c0040t0003g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.125+7434G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140529 | ||||||
| chr12:121140548
|
T | C | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+7453T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140548 | ||||||
| chr12:121140584
|
T | C | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+7489T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140584 | ||||||
| chr12:121140647
|
G | A | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+7552G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140647 | ||||||
| chr12:121140762
|
A | C | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+7667A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140762 | ||||||
| chr12:121140809
|
A | C | 1 | a0022c0025t0015g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.125+7714A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140809 | ||||||
| chr12:121140816
|
G | A | 1 | a0010c0010t0011g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.125+7721G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140816 | ||||||
| chr12:121140919
|
C | A | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+7824C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140919 | ||||||
| chr12:121140922
|
C | A | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+7827C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121140922 | ||||||
| chr12:121141023
|
T | C | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.125+7928T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141023 | ||||||
| chr12:121141188
|
C | G | 1 | a0014c0014t0003g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.125+8093C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141188 | ||||||
| chr12:121141189
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.125+8094C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141189 | ||||||
| chr12:121141221
|
T | G | 12 | a0001c0001t0001g0159a0002c0002t0001g0079a0002c0002t0001g0118others(9): Show | 13 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.125+8126T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141221 | ||||||
| chr12:121141273
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.125+8178G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141273 | ||||||
| chr12:121141275
|
A | G | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+8180A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141275 | ||||||
| chr12:121141337
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0360others(5): Show | 8 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.125+8242G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141337 | ||||||
| chr12:121141487
|
G | C | 12 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(9): Show | 12 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.125+8392G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141487 | ||||||
| chr12:121141489
|
T | G | 1 | a0001c0001t0034g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125+8394T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141489 | ||||||
| chr12:121141572
|
AGCTGTCC others(7): Show |
A | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.125+8478_125+8491d others(16): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141572 | ||||||
| chr12:121141609
|
T | C | 7 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.125+8514T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141609 | ||||||
| chr12:121141713
|
G | C | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+8618G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141713 | ||||||
| chr12:121141723
|
G | A | 50 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.125+8628G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141723 | ||||||
| chr12:121141846
|
G | A | 1 | a0005c0006t0003g0327 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.125+8751G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141846 | ||||||
| chr12:121141854
|
C | A | 126 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(123): Show | 126 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.125+8759C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141854 | ||||||
| chr12:121141870
|
C | T | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+8775C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141870 | ||||||
| chr12:121141918
|
A | G | 66 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(63): Show | 67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.125+8823A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121141918 | ||||||
| chr12:121142020
|
G | A | 1 | a0004c0003t0027g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.125+8925G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142020 | ||||||
| chr12:121142122
|
A | G | 6 | a0002c0002t0003g0338a0002c0002t0035g0343a0005c0006t0003g0327others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.125+9027A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142122 | ||||||
| chr12:121142152
|
G | A | 51 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.125+9057G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142152 | ||||||
| chr12:121142307
|
A | G | 3 | a0018c0034t0005g0258a0024c0027t0021g0197a0030c0031t0002g0202 | 3 | HG01243.hp2 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.125+9212A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142307 | ||||||
| chr12:121142420
|
G | A | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+9325G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142420 | ||||||
| chr12:121142438
|
A | T | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.125+9343A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142438 | ||||||
| chr12:121142591
|
G | A | 1 | a0008c0007t0002g0218 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.125+9496G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142591 | ||||||
| chr12:121142595
|
G | A | 1 | a0004c0003t0004g0220 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.125+9500G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142595 | ||||||
| chr12:121142661
|
T | C | 51 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.125+9566T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142661 | ||||||
| chr12:121142675
|
T | G | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.125+9580T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142675 | ||||||
| chr12:121142738
|
C | T | 51 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.125+9643C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142738 | ||||||
| chr12:121142917
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0096 | 3 | NA18994.hp1 NA19003.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.125+9822T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142917 | ||||||
| chr12:121142950
|
G | A | 49 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(46): Show | 49 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.125+9855G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142950 | ||||||
| chr12:121142967
|
G | T | 1 | a0022c0025t0015g0204 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.125+9872G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121142967 | ||||||
| chr12:121143045
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.125+9950C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143045 | ||||||
| chr12:121143061
|
G | A | 11 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.125+9966G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143061 | ||||||
| chr12:121143073
|
C | A | 1 | a0002c0002t0035g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.125+9978C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143073 | ||||||
| chr12:121143081
|
C | CAAA | 46 | a0002c0002t0001g0228a0002c0002t0001g0243a0002c0002t0003g0185others(43): Show | 46 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.125+9998_125+10000 others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121143081 | |||||
| chr12:121143173
|
A | T | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.125+10078A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143173 | ||||||
| chr12:121143182
|
G | A | 51 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(48): Show | 51 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.125+10087G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143182 | ||||||
| chr12:121143221
|
TA | T | 125 | a0001c0001t0001g0331a0002c0002t0001g0228a0002c0002t0001g0243others(122): Show | 125 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.125+10141delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121143221 | |||||
| chr12:121143235
|
A | T | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.125+10140A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143235 | ||||||
| chr12:121143237
|
T | C | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.125+10142T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143237 | ||||||
| chr12:121143424
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0027others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.125+10329C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143424 | ||||||
| chr12:121143676
|
C | G | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.125+10581C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143676 | ||||||
| chr12:121143697
|
A | G | 1 | a0004c0003t0027g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.125+10602A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143697 | ||||||
| chr12:121143815
|
G | A | 30 | a0001c0001t0017g0161a0003c0004t0001g0038a0003c0004t0001g0054others(27): Show | 30 | HG00438.hp2 HG02004.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.125+10720G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143815 | ||||||
| chr12:121143828
|
G | A | 1 | a0015c0012t0014g0031 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.125+10733G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143828 | ||||||
| chr12:121143858
|
A | T | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+10763A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143858 | ||||||
| chr12:121143878
|
T | C | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.125+10783T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143878 | ||||||
| chr12:121143914
|
G | A | 1 | a0019c0022t0005g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.125+10819G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143914 | ||||||
| chr12:121143935
|
T | C | 64 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(61): Show | 65 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.125+10840T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143935 | ||||||
| chr12:121143936
|
G | A | 1 | a0017c0020t0002g0359 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.125+10841G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121143936 | ||||||
| chr12:121144113
|
T | C | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126-10672T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144113 | ||||||
| chr12:121144179
|
G | T | 75 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(72): Show | 75 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.126-10606G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144179 | ||||||
| chr12:121144180
|
C | T | 75 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(72): Show | 75 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.126-10605C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144180 | ||||||
| chr12:121144245
|
T | C | 75 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(72): Show | 75 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.126-10540T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144245 | ||||||
| chr12:121144277
|
G | A | 1 | a0006c0005t0002g0070 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.126-10508G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144277 | ||||||
| chr12:121144437
|
G | A | 192 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(189): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.126-10348G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144437 | ||||||
| chr12:121144447
|
C | A | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-10338C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144447 | ||||||
| chr12:121144905
|
G | A | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.126-9880G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144905 | ||||||
| chr12:121144906
|
A | T | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.126-9879A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144906 | ||||||
| chr12:121144907
|
T | A | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.126-9878T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144907 | ||||||
| chr12:121144986
|
G | A | 1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.126-9799G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121144986 | ||||||
| chr12:121145100
|
A | C | 1 | a0009c0009t0006g0277 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.126-9685A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145100 | ||||||
| chr12:121145278
|
C | T | 1 | a0003c0004t0001g0113 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.126-9507C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145278 | ||||||
| chr12:121145346
|
T | A | 1 | a0014c0014t0003g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126-9439T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145346 | ||||||
| chr12:121145353
|
T | C | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126-9432T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145353 | ||||||
| chr12:121145447
|
G | A | 1 | a0006c0005t0002g0060 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.126-9338G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145447 | ||||||
| chr12:121145460
|
C | G | 1 | a0004c0003t0011g0133 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.126-9325C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145460 | ||||||
| chr12:121145464
|
A | T | 1 | a0003c0004t0001g0156 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.126-9321A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145464 | ||||||
| chr12:121145490
|
C | CCTTT | 16 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(13): Show | 17 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.126-9287_126-9284d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121145490 | |||||
| chr12:121145510
|
C | CT | 18 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0092others(15): Show | 19 | HG01123.hp2 HG01168.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.126-9261dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121145510 | |||||
| chr12:121145510
|
CT | C | 77 | a0001c0001t0001g0034a0001c0001t0001g0331a0002c0002t0001g0285others(74): Show | 77 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.126-9261delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121145510 | |||||
| chr12:121145546
|
G | A | 1 | a0031c0036t0002g0225 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.126-9239G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145546 | ||||||
| chr12:121145602
|
G | A | 1 | a0003c0004t0003g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.126-9183G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145602 | ||||||
| chr12:121145617
|
C | T | 2 | a0013c0018t0004g0028a0013c0018t0004g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.126-9168C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145617 | ||||||
| chr12:121145722
|
G | A | 1 | a0012c0013t0005g0020 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.126-9063G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145722 | ||||||
| chr12:121145786
|
G | C | 8 | a0002c0002t0001g0228a0004c0003t0004g0221a0004c0003t0004g0226others(5): Show | 8 | HG00558.hp1 HG02071.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.126-8999G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145786 | ||||||
| chr12:121145948
|
C | G | 196 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(193): Show | 197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.126-8837C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145948 | ||||||
| chr12:121145949
|
G | A | 3 | a0006c0005t0002g0043a0006c0005t0002g0061a0006c0005t0024g0139 | 3 | HG01978.hp2 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.126-8836G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145949 | ||||||
| chr12:121145960
|
G | C | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-8825G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121145960 | ||||||
| chr12:121146025
|
G | A | 9 | a0004c0003t0004g0206a0004c0003t0012g0199a0004c0003t0012g0201others(6): Show | 9 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.126-8760G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146025 | ||||||
| chr12:121146101
|
T | C | 2 | a0005c0006t0001g0337a0005c0006t0001g0341 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.126-8684T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146101 | ||||||
| chr12:121146134
|
A | G | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-8651A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146134 | ||||||
| chr12:121146190
|
C | T | 6 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-8595C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146190 | ||||||
| chr12:121146251
|
A | G | 14 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0092others(11): Show | 15 | HG01123.hp2 HG01978.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.126-8534A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146251 | ||||||
| chr12:121146287
|
C | CT | 34 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0042others(31): Show | 34 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.126-8469dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121146287 | |||||
| chr12:121146287
|
CT | C | 120 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0132others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.126-8469delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121146287 | |||||
| chr12:121146287
|
CTT | C | 31 | a0002c0002t0003g0185a0002c0002t0003g0323a0002c0024t0001g0283others(28): Show | 32 | HG01074.hp2 HG01099.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.126-8470_126-8469d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121146287 | |||||
| chr12:121146287
|
CTTT | C | 8 | a0011c0011t0005g0177a0011c0011t0005g0178a0011c0011t0005g0179others(5): Show | 8 | HG00280.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-8471_126-8469d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121146287 | |||||
| chr12:121146287
|
CTTTTT | C | 6 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-8473_126-8469d others(7): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121146287 | |||||
| chr12:121146287
|
CTTTTTTT others(3): Show |
C | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126-8478_126-8469d others(12): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121146287 | |||||
| chr12:121146357
|
A | G | 107 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(104): Show | 107 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.126-8428A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146357 | ||||||
| chr12:121146535
|
C | G | 15 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-8250C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146535 | ||||||
| chr12:121146568
|
A | G | 15 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-8217A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146568 | ||||||
| chr12:121146571
|
G | A | 18 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(15): Show | 19 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.126-8214G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146571 | ||||||
| chr12:121146595
|
C | T | 15 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-8190C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146595 | ||||||
| chr12:121146607
|
G | A | 10 | a0002c0002t0003g0185a0002c0002t0003g0198a0002c0024t0001g0283others(7): Show | 10 | HG00280.hp2 HG01358.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-8178G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146607 | ||||||
| chr12:121146681
|
C | G | 15 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.126-8104C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146681 | ||||||
| chr12:121146718
|
G | A | 2 | a0004c0003t0004g0206a0005c0006t0001g0352 | 2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.126-8067G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146718 | ||||||
| chr12:121146878
|
C | T | 6 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-7907C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146878 | ||||||
| chr12:121146945
|
G | C | 1 | a0034c0046t0002g0297 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.126-7840G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146945 | ||||||
| chr12:121146987
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.126-7798A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146987 | ||||||
| chr12:121146999
|
G | A | 1 | a0008c0007t0002g0318 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.126-7786G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121146999 | ||||||
| chr12:121147076
|
C | CA | 17 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(14): Show | 18 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.126-7709_126-7708i others(3): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121147076 | ||||||
| chr12:121147187
|
G | A | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-7598G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121147187 | ||||||
| chr12:121147221
|
T | C | 14 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(11): Show | 15 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.126-7564T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121147221 | ||||||
| chr12:121147425
|
A | C | 6 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-7360A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121147425 | ||||||
| chr12:121147599
|
T | TTTG | 132 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(129): Show | 133 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.126-7177_126-7175d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121147599 | |||||
| chr12:121147599
|
T | TTTTG | 54 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(51): Show | 54 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.126-7184_126-7183i others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121147599 | |||||
| chr12:121147605
|
G | GTTGTTGT | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-7175_126-7174i others(9): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121147605 | |||||
| chr12:121147608
|
GT | G | 3 | a0018c0034t0005g0258a0024c0027t0021g0197a0030c0031t0002g0202 | 3 | HG01243.hp2 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.126-7174delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121147608 | |||||
| chr12:121148139
|
T | A | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-6646T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148139 | ||||||
| chr12:121148188
|
T | TTTTA | 96 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0047others(93): Show | 98 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.126-6557_126-6554d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121148188 | |||||
| chr12:121148188
|
T | TTTTATTT others(1): Show |
21 | a0002c0002t0001g0079a0002c0002t0001g0118a0002c0002t0001g0171others(18): Show | 21 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.126-6561_126-6554d others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121148188 | |||||
| chr12:121148188
|
T | TTTTATTT others(5): Show |
4 | a0010c0010t0011g0278a0010c0010t0011g0279a0010c0010t0011g0280others(1): Show | 4 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-6565_126-6554d others(14): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121148188 | |||||
| chr12:121148188
|
TTTTA | T | 8 | a0004c0003t0012g0199a0004c0003t0012g0205a0004c0003t0031g0203others(5): Show | 8 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.126-6557_126-6554d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121148188 | |||||
| chr12:121148188
|
TTTTATTT others(1): Show |
T | 3 | a0018c0034t0005g0258a0024c0027t0021g0197a0030c0031t0002g0202 | 3 | HG01243.hp2 HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.126-6561_126-6554d others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121148188 | |||||
| chr12:121148192
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.126-6593A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148192 | ||||||
| chr12:121148233
|
G | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0027others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.126-6552G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148233 | ||||||
| chr12:121148246
|
A | G | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-6539A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148246 | ||||||
| chr12:121148293
|
C | T | 1 | a0008c0007t0002g0334 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.126-6492C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148293 | ||||||
| chr12:121148304
|
T | C | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-6481T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148304 | ||||||
| chr12:121148370
|
G | T | 24 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(21): Show | 25 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.126-6415G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148370 | ||||||
| chr12:121148559
|
C | T | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126-6226C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148559 | ||||||
| chr12:121148568
|
C | T | 1 | a0004c0003t0027g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.126-6217C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148568 | ||||||
| chr12:121148592
|
A | G | 70 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.126-6193A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148592 | ||||||
| chr12:121148621
|
G | T | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126-6164G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148621 | ||||||
| chr12:121148704
|
G | A | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126-6081G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148704 | ||||||
| chr12:121148773
|
G | A | 3 | a0007c0008t0001g0016a0007c0008t0001g0017a0007c0008t0001g0018 | 3 | HG02280.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.126-6012G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148773 | ||||||
| chr12:121148798
|
G | A | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-5987G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148798 | ||||||
| chr12:121148867
|
C | A | 1 | a0034c0046t0002g0297 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.126-5918C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148867 | ||||||
| chr12:121148965
|
A | G | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-5820A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121148965 | ||||||
| chr12:121149024
|
G | A | 30 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(27): Show | 31 | HG01099.hp1 HG01109.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.126-5761G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149024 | ||||||
| chr12:121149097
|
C | T | 10 | a0002c0002t0003g0252a0002c0002t0003g0253a0002c0002t0003g0255others(7): Show | 10 | HG02055.hp2 HG02559.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.126-5688C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149097 | ||||||
| chr12:121149136
|
T | C | 3 | a0007c0008t0001g0016a0007c0008t0001g0017a0007c0008t0001g0018 | 3 | HG02280.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.126-5649T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149136 | ||||||
| chr12:121149231
|
C | T | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-5554C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149231 | ||||||
| chr12:121149234
|
T | A | 4 | a0003c0004t0001g0094a0003c0004t0001g0120a0003c0004t0001g0128others(1): Show | 4 | HG02129.hp1 NA19009.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-5551T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149234 | ||||||
| chr12:121149340
|
C | T | 2 | a0003c0004t0001g0094a0003c0004t0001g0128 | 2 | HG02129.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.126-5445C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149340 | ||||||
| chr12:121149541
|
T | C | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-5244T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149541 | ||||||
| chr12:121149543
|
C | T | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-5242C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149543 | ||||||
| chr12:121149550
|
T | C | 193 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.126-5235T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149550 | ||||||
| chr12:121149603
|
G | A | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-5182G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149603 | ||||||
| chr12:121149778
|
C | T | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.126-5007C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149778 | ||||||
| chr12:121149840
|
G | A | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-4945G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149840 | ||||||
| chr12:121149891
|
T | C | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-4894T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121149891 | ||||||
| chr12:121150003
|
G | A | 1 | a0001c0043t0001g0089 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.126-4782G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150003 | ||||||
| chr12:121150170
|
T | G | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-4615T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150170 | ||||||
| chr12:121150285
|
G | C | 50 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(47): Show | 50 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.126-4500G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150285 | ||||||
| chr12:121150322
|
C | T | 6 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-4463C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150322 | ||||||
| chr12:121150422
|
G | A | 1 | a0036c0047t0001g0304 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.126-4363G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150422 | ||||||
| chr12:121150488
|
G | A | 1 | a0011c0011t0004g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.126-4297G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150488 | ||||||
| chr12:121150498
|
G | A | 5 | a0001c0001t0001g0076a0002c0002t0036g0056a0013c0018t0004g0028others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.126-4287G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150498 | ||||||
| chr12:121150518
|
C | T | 1 | a0007c0008t0001g0348 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.126-4267C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150518 | ||||||
| chr12:121150538
|
G | A | 1 | a0006c0005t0023g0071 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.126-4247G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150538 | ||||||
| chr12:121150742
|
T | C | 193 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.126-4043T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150742 | ||||||
| chr12:121150758
|
A | C | 1 | a0010c0010t0006g0264 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.126-4027A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150758 | ||||||
| chr12:121150903
|
C | T | 6 | a0007c0008t0001g0016a0007c0008t0001g0017a0007c0008t0001g0018others(3): Show | 6 | HG02280.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-3882C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150903 | ||||||
| chr12:121150904
|
G | A | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-3881G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150904 | ||||||
| chr12:121150959
|
A | T | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-3826A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121150959 | ||||||
| chr12:121151116
|
T | C | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-3669T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151116 | ||||||
| chr12:121151396
|
C | T | 12 | a0001c0001t0001g0159a0002c0002t0001g0079a0002c0002t0001g0118others(9): Show | 13 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.126-3389C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151396 | ||||||
| chr12:121151522
|
A | G | 4 | a0001c0001t0001g0151a0001c0001t0001g0169a0006c0005t0002g0164others(1): Show | 4 | HG01123.hp2 HG01978.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.126-3263A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151522 | ||||||
| chr12:121151596
|
T | C | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-3189T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151596 | ||||||
| chr12:121151600
|
TA | T | 13 | a0002c0024t0001g0283a0002c0024t0003g0186a0003c0004t0003g0187others(10): Show | 13 | HG00280.hp2 HG01243.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.126-3179delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121151600 | |||||
| chr12:121151609
|
T | A | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-3176T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151609 | ||||||
| chr12:121151639
|
C | T | 1 | a0005c0006t0003g0358 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.126-3146C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151639 | ||||||
| chr12:121151659
|
A | G | 71 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(68): Show | 71 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.126-3126A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151659 | ||||||
| chr12:121151676
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.126-3109G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151676 | ||||||
| chr12:121151712
|
C | G | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.126-3073C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151712 | ||||||
| chr12:121151828
|
C | G | 1 | a0033c0041t0001g0126 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.126-2957C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151828 | ||||||
| chr12:121151905
|
A | G | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-2880A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121151905 | ||||||
| chr12:121152015
|
A | T | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-2770A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152015 | ||||||
| chr12:121152122
|
G | A | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-2663G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152122 | ||||||
| chr12:121152140
|
C | T | 1 | a0004c0003t0004g0219 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.126-2645C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152140 | ||||||
| chr12:121152173
|
G | A | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-2612G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152173 | ||||||
| chr12:121152228
|
A | G | 3 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216 | 3 | HG02818.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.126-2557A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152228 | ||||||
| chr12:121152228
|
A | T | 1 | a0001c0001t0034g0111 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.126-2557A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152228 | ||||||
| chr12:121152262
|
T | G | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126-2523T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152262 | ||||||
| chr12:121152421
|
C | T | 1 | a0022c0025t0015g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126-2364C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152421 | ||||||
| chr12:121152551
|
T | C | 193 | a0001c0001t0001g0331a0002c0002t0001g0228a0002c0002t0001g0243others(190): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.126-2234T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152551 | ||||||
| chr12:121152674
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-2111C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152674 | ||||||
| chr12:121152847
|
T | C | 19 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(16): Show | 19 | NA18945.hp2 NA18946.hp1 NA18947.hp1 others(16): Show |
intron_variant | MODIFIER | c.126-1938T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152847 | ||||||
| chr12:121152913
|
C | T | 1 | a0018c0034t0005g0258 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.126-1872C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152913 | ||||||
| chr12:121152944
|
G | A | 6 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(3): Show | 6 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-1841G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121152944 | ||||||
| chr12:121153008
|
T | C | 24 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(21): Show | 24 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.126-1777T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153008 | ||||||
| chr12:121153139
|
A | T | 1 | a0002c0002t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.126-1646A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153139 | ||||||
| chr12:121153146
|
C | T | 40 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.126-1639C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153146 | ||||||
| chr12:121153361
|
A | C | 1 | a0028c0040t0003g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.126-1424A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153361 | ||||||
| chr12:121153499
|
G | A | 2 | a0007c0008t0001g0074a0008c0039t0028g0012 | 2 | HG02080.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.126-1286G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153499 | ||||||
| chr12:121153542
|
G | A | 1 | a0020c0023t0009g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.126-1243G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153542 | ||||||
| chr12:121153572
|
G | C | 1 | a0003c0004t0001g0086 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.126-1213G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153572 | ||||||
| chr12:121153677
|
C | CA | 44 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(41): Show | 44 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.126-1101dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121153677 | |||||
| chr12:121153778
|
T | C | 1 | a0017c0020t0002g0335 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.126-1007T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153778 | ||||||
| chr12:121153829
|
G | A | 25 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(22): Show | 25 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.126-956G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153829 | ||||||
| chr12:121153883
|
A | G | 1 | a0001c0001t0001g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.126-902A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153883 | ||||||
| chr12:121153945
|
C | G | 6 | a0003c0004t0001g0086a0003c0004t0001g0117a0003c0004t0001g0157others(3): Show | 6 | HG02004.hp1 HG02040.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.126-840C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153945 | ||||||
| chr12:121153981
|
G | A | 1 | a0003c0004t0001g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.126-804G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121153981 | ||||||
| chr12:121154128
|
T | TA | 22 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(19): Show | 22 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.126-647dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121154128 | |||||
| chr12:121154275
|
A | G | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.126-510A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121154275 | ||||||
| chr12:121154290
|
C | CA | 96 | a0001c0001t0001g0068a0001c0001t0001g0331a0002c0002t0001g0227others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.126-482dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 121154290 | |||||
| chr12:121154334
|
A | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-451A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121154334 | ||||||
| chr12:121154379
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.126-406G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121154379 | ||||||
| chr12:121154433
|
C | T | 1 | a0004c0003t0004g0220 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.126-352C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121154433 | ||||||
| chr12:121154463
|
G | A | 1 | a0022c0025t0015g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.126-322G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121154463 | ||||||
| chr12:121154665
|
C | T | 9 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.126-120C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121154665 | ||||||
| chr12:121154774
|
C | T | 2 | a0007c0008t0001g0307a0019c0022t0005g0308 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.126-11C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 1/12 | chr12 | 121154774 | ||||||
| chr12:121155059
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+106C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155059 | ||||||
| chr12:121155163
|
T | C | 1 | a0008c0007t0002g0324 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.294+210T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155163 | ||||||
| chr12:121155216
|
C | T | 109 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.294+263C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155216 | ||||||
| chr12:121155231
|
C | T | 1 | a0002c0002t0001g0295 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.294+278C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155231 | ||||||
| chr12:121155232
|
G | A | 4 | a0006c0005t0002g0099a0006c0005t0002g0100a0006c0005t0002g0106others(1): Show | 4 | HG01975.hp2 HG01981.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+279G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155232 | ||||||
| chr12:121155365
|
C | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.294+412C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155365 | ||||||
| chr12:121155422
|
G | A | 1 | a0006c0005t0024g0139 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.294+469G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155422 | ||||||
| chr12:121155470
|
G | A | 1 | a0012c0042t0005g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.294+517G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155470 | ||||||
| chr12:121155544
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.295-535G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155544 | ||||||
| chr12:121155552
|
C | A | 40 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.295-527C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155552 | ||||||
| chr12:121155568
|
C | T | 40 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(37): Show | 40 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.295-511C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155568 | ||||||
| chr12:121155569
|
G | A | 3 | a0007c0008t0001g0307a0018c0034t0005g0258a0019c0022t0005g0308 | 3 | HG02109.hp2 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.295-510G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155569 | ||||||
| chr12:121155578
|
A | G | 121 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(118): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.295-501A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155578 | ||||||
| chr12:121155580
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-499C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155580 | ||||||
| chr12:121155698
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-381T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155698 | ||||||
| chr12:121155792
|
T | TA | 9 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.295-277dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 121155792 | |||||
| chr12:121155792
|
TAAAAAAA others(5): Show |
T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.295-282_295-271del others(12): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 121155792 | |||||
| chr12:121155797
|
A | C | 9 | a0004c0003t0004g0236a0004c0003t0020g0245a0007c0008t0001g0010others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.295-282A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155797 | ||||||
| chr12:121155802
|
AC | A | 13 | a0002c0002t0003g0252a0002c0002t0003g0253a0002c0002t0003g0255others(10): Show | 13 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.295-276delC | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155802 | ||||||
| chr12:121155809
|
C | A | 1 | a0004c0003t0007g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.295-270C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155809 | ||||||
| chr12:121155895
|
C | A | 1 | a0029c0037t0001g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.295-184C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121155895 | ||||||
| chr12:121156044
|
G | C | 1 | a0008c0007t0002g0288 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.295-35G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121156044 | ||||||
| chr12:121156049
|
T | TGCATTTT others(4): Show |
1 | a0002c0002t0001g0227 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.295-27_295-17dupAT others(9): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 121156049 | |||||
| chr12:121156068
|
C | T | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.295-11C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 2/12 | chr12 | 121156068 | ||||||
| chr12:121156181
|
T | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+34T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156181 | ||||||
| chr12:121156208
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+61C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156208 | ||||||
| chr12:121156253
|
G | A | 191 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(188): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.363+106G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156253 | ||||||
| chr12:121156367
|
G | A | 43 | a0002c0002t0003g0185a0002c0002t0003g0198a0002c0002t0003g0252others(40): Show | 44 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.363+220G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156367 | ||||||
| chr12:121156380
|
A | T | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.363+233A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156380 | ||||||
| chr12:121156401
|
C | T | 6 | a0003c0004t0001g0003a0003c0004t0001g0015a0003c0004t0001g0026others(3): Show | 7 | HG01071.hp2 HG01243.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.363+254C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156401 | ||||||
| chr12:121156437
|
C | A | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+290C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156437 | ||||||
| chr12:121156486
|
T | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+339T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156486 | ||||||
| chr12:121156530
|
A | G | 1 | a0006c0005t0029g0007 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.363+383A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156530 | ||||||
| chr12:121156652
|
T | C | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.363+505T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156652 | ||||||
| chr12:121156657
|
T | G | 43 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.363+510T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156657 | ||||||
| chr12:121156743
|
G | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+596G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156743 | ||||||
| chr12:121156769
|
C | T | 1 | a0022c0025t0015g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.363+622C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156769 | ||||||
| chr12:121156794
|
C | T | 1 | a0020c0023t0037g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.363+647C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156794 | ||||||
| chr12:121156881
|
T | C | 195 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(192): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.363+734T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156881 | ||||||
| chr12:121156893
|
C | T | 1 | a0031c0036t0002g0225 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.363+746C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156893 | ||||||
| chr12:121156929
|
G | A | 1 | a0008c0007t0002g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.363+782G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156929 | ||||||
| chr12:121156998
|
A | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+851A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121156998 | ||||||
| chr12:121157039
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+892T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157039 | ||||||
| chr12:121157050
|
C | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+903C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157050 | ||||||
| chr12:121157090
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+943C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157090 | ||||||
| chr12:121157091
|
G | A | 24 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(21): Show | 24 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.363+944G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157091 | ||||||
| chr12:121157137
|
C | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+990C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157137 | ||||||
| chr12:121157150
|
G | A | 1 | a0012c0013t0005g0146 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.363+1003G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157150 | ||||||
| chr12:121157180
|
A | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1033A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157180 | ||||||
| chr12:121157189
|
G | A | 6 | a0004c0003t0004g0206a0005c0017t0005g0214a0005c0017t0005g0215others(3): Show | 6 | HG02818.hp2 HG03041.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+1042G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157189 | ||||||
| chr12:121157251
|
G | A | 4 | a0002c0002t0003g0198a0007c0008t0001g0307a0018c0034t0005g0258others(1): Show | 4 | HG02109.hp2 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+1104G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157251 | ||||||
| chr12:121157278
|
T | C | 1 | a0002c0002t0003g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.363+1131T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157278 | ||||||
| chr12:121157383
|
A | G | 5 | a0010c0010t0011g0278a0010c0010t0011g0279a0010c0010t0011g0280others(2): Show | 5 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+1236A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157383 | ||||||
| chr12:121157390
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1243C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157390 | ||||||
| chr12:121157416
|
G | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1269G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157416 | ||||||
| chr12:121157544
|
C | G | 1 | a0020c0023t0009g0160 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.363+1397C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157544 | ||||||
| chr12:121157568
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1421C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157568 | ||||||
| chr12:121157650
|
T | C | 1 | a0003c0004t0001g0361 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.363+1503T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157650 | ||||||
| chr12:121157820
|
C | A | 1 | a0022c0025t0015g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.363+1673C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157820 | ||||||
| chr12:121157840
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1693T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157840 | ||||||
| chr12:121157872
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1725G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157872 | ||||||
| chr12:121157884
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1737G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157884 | ||||||
| chr12:121157897
|
T | A | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.363+1750T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157897 | ||||||
| chr12:121157933
|
T | C | 2 | a0018c0026t0016g0080a0018c0026t0016g0081 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.363+1786T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121157933 | ||||||
| chr12:121158126
|
C | T | 1 | a0004c0003t0004g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.363+1979C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158126 | ||||||
| chr12:121158336
|
G | A | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.363+2189G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158336 | ||||||
| chr12:121158356
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+2209G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158356 | ||||||
| chr12:121158372
|
C | A | 2 | a0002c0002t0001g0285a0008c0007t0002g0288 | 2 | HG00438.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.363+2225C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158372 | ||||||
| chr12:121158388
|
A | G | 70 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.363+2241A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158388 | ||||||
| chr12:121158559
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-2343G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158559 | ||||||
| chr12:121158560
|
C | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-2342C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158560 | ||||||
| chr12:121158609
|
C | T | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.364-2293C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158609 | ||||||
| chr12:121158706
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.364-2196T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158706 | ||||||
| chr12:121158733
|
T | TA | 28 | a0003c0004t0001g0120a0005c0017t0005g0214a0005c0017t0005g0215others(25): Show | 28 | HG01074.hp2 HG01258.hp1 HG01943.hp1 others(25): Show |
intron_variant | MODIFIER | c.364-2159dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121158733 | |||||
| chr12:121158734
|
A | T | 5 | a0003c0004t0001g0038a0003c0004t0001g0055a0007c0008t0001g0016others(2): Show | 5 | HG02280.hp1 HG02559.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-2168A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158734 | ||||||
| chr12:121158753
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-2149C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158753 | ||||||
| chr12:121158841
|
A | G | 70 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.364-2061A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158841 | ||||||
| chr12:121158983
|
C | T | 27 | a0002c0002t0003g0185a0004c0003t0012g0199a0004c0003t0012g0201others(24): Show | 28 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.364-1919C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121158983 | ||||||
| chr12:121159156
|
C | T | 16 | a0002c0024t0001g0283a0002c0024t0003g0186a0003c0004t0003g0187others(13): Show | 16 | HG00280.hp2 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.364-1746C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159156 | ||||||
| chr12:121159323
|
A | C | 1 | a0002c0002t0001g0315 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.364-1579A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159323 | ||||||
| chr12:121159417
|
C | CA | 54 | a0001c0001t0001g0103a0001c0001t0001g0135a0001c0001t0034g0111others(51): Show | 54 | HG00280.hp2 HG00558.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.364-1462dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121159417 | |||||
| chr12:121159417
|
C | CAA | 91 | a0001c0001t0001g0331a0002c0002t0001g0227a0002c0002t0001g0228others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.364-1463_364-1462d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121159417 | |||||
| chr12:121159417
|
C | CAAA | 15 | a0002c0002t0001g0285a0002c0002t0003g0298a0002c0002t0035g0343others(12): Show | 15 | HG00438.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.364-1464_364-1462d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121159417 | |||||
| chr12:121159417
|
CA | C | 18 | a0001c0001t0001g0030a0002c0002t0003g0252a0002c0002t0003g0253others(15): Show | 18 | HG00280.hp1 HG00423.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.364-1462delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121159417 | |||||
| chr12:121159471
|
G | T | 1 | a0018c0034t0005g0258 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.364-1431G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159471 | ||||||
| chr12:121159603
|
A | T | 2 | a0013c0018t0004g0175a0013c0018t0004g0188 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.364-1299A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159603 | ||||||
| chr12:121159610
|
G | A | 96 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(93): Show | 97 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.364-1292G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159610 | ||||||
| chr12:121159612
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1290C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159612 | ||||||
| chr12:121159621
|
A | G | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.364-1281A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159621 | ||||||
| chr12:121159639
|
C | T | 1 | a0022c0025t0015g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.364-1263C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159639 | ||||||
| chr12:121159749
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1153C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159749 | ||||||
| chr12:121159778
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG00423.hp1 HG02155.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1124C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159778 | ||||||
| chr12:121159801
|
C | G | 1 | a0002c0002t0001g0171 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.364-1101C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159801 | ||||||
| chr12:121159828
|
G | A | 43 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.364-1074G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159828 | ||||||
| chr12:121159890
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1012C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159890 | ||||||
| chr12:121159895
|
C | T | 15 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.364-1007C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121159895 | ||||||
| chr12:121160090
|
CTTCT | C | 13 | a0002c0002t0003g0252a0002c0002t0003g0253a0002c0002t0003g0255others(10): Show | 13 | HG02055.hp2 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.364-801_364-798del others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121160090 | |||||
| chr12:121160101
|
C | CT | 34 | a0001c0001t0001g0069a0001c0001t0001g0091a0002c0002t0001g0227others(31): Show | 34 | HG00438.hp2 HG01106.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.364-792dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121160101 | |||||
| chr12:121160116
|
C | CTT | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-784_364-783dup others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121160116 | |||||
| chr12:121160126
|
T | TTC | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-775_364-774ins others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 121160126 | |||||
| chr12:121160133
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-769T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160133 | ||||||
| chr12:121160137
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-765T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160137 | ||||||
| chr12:121160173
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-729G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160173 | ||||||
| chr12:121160272
|
C | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-630C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160272 | ||||||
| chr12:121160295
|
A | C | 6 | a0003c0004t0001g0003a0003c0004t0001g0015a0003c0004t0001g0026others(3): Show | 7 | HG01071.hp2 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.364-607A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160295 | ||||||
| chr12:121160336
|
G | A | 2 | a0001c0001t0001g0149a0002c0002t0001g0286 | 2 | HG00423.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.364-566G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160336 | ||||||
| chr12:121160426
|
C | T | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.364-476C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160426 | ||||||
| chr12:121160432
|
A | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-470A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160432 | ||||||
| chr12:121160439
|
G | A | 3 | a0007c0008t0001g0016a0007c0008t0001g0017a0007c0008t0001g0018 | 3 | HG02280.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.364-463G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160439 | ||||||
| chr12:121160441
|
C | T | 70 | a0001c0001t0001g0331a0002c0002t0001g0285a0002c0002t0001g0286others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.364-461C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160441 | ||||||
| chr12:121160558
|
A | G | 2 | a0013c0018t0004g0028a0013c0018t0004g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.364-344A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160558 | ||||||
| chr12:121160634
|
A | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-268A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160634 | ||||||
| chr12:121160645
|
C | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-257C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160645 | ||||||
| chr12:121160684
|
C | A | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.364-218C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160684 | ||||||
| chr12:121160762
|
G | A | 39 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-140G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160762 | ||||||
| chr12:121160849
|
G | A | 39 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0243others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-53G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 3/12 | chr12 | 121160849 | ||||||
| chr12:121160988
|
C | A | 2 | a0019c0022t0005g0196a0022c0025t0015g0195 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.436+14C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121160988 | ||||||
| chr12:121161125
|
CTCTGTCC others(37): Show |
C | 1 | a0010c0010t0006g0263 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.436+153_436+196del others(44): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 121161125 | |||||
| chr12:121161161
|
T | G | 1 | a0001c0001t0003g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.436+187T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161161 | ||||||
| chr12:121161415
|
G | T | 3 | a0007c0008t0001g0051a0018c0026t0016g0080a0018c0026t0016g0081 | 3 | HG02683.hp2 HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.436+441G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161415 | ||||||
| chr12:121161431
|
T | G | 1 | a0005c0006t0009g0193 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.436+457T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161431 | ||||||
| chr12:121161446
|
T | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+472T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161446 | ||||||
| chr12:121161510
|
GCAGCGAG others(24): Show |
G | 1 | a0015c0012t0012g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.436+541_436+571del others(31): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 121161510 | |||||
| chr12:121161518
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+544C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161518 | ||||||
| chr12:121161528
|
G | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+554G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161528 | ||||||
| chr12:121161590
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0360 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.436+616G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161590 | ||||||
| chr12:121161697
|
C | T | 2 | a0007c0008t0001g0307a0019c0022t0005g0308 | 2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.436+723C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161697 | ||||||
| chr12:121161735
|
T | A | 1 | a0002c0002t0001g0286 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.437-689T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161735 | ||||||
| chr12:121161751
|
C | T | 9 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.437-673C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161751 | ||||||
| chr12:121161760
|
C | T | 1 | a0002c0002t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.437-664C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161760 | ||||||
| chr12:121161789
|
T | TA | 141 | a0001c0001t0001g0331a0002c0002t0001g0228a0002c0002t0001g0243others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.437-620dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 121161789 | |||||
| chr12:121161834
|
AT | A | 15 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.437-589delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161834 | ||||||
| chr12:121161838
|
T | TA | 45 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(42): Show | 46 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.437-573dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 121161838 | |||||
| chr12:121161934
|
A | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-490A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161934 | ||||||
| chr12:121161983
|
G | A | 1 | a0019c0022t0005g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.437-441G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121161983 | ||||||
| chr12:121162023
|
C | T | 7 | a0002c0002t0035g0343a0002c0002t0036g0056a0005c0006t0001g0337others(4): Show | 7 | HG01168.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-401C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121162023 | ||||||
| chr12:121162026
|
G | C | 24 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(21): Show | 24 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.437-398G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121162026 | ||||||
| chr12:121162143
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-281G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121162143 | ||||||
| chr12:121162294
|
C | G | 5 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(2): Show | 5 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-130C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121162294 | ||||||
| chr12:121162337
|
G | A | 2 | a0010c0010t0025g0281a0025c0029t0003g0282 | 2 | HG01943.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.437-87G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121162337 | ||||||
| chr12:121162377
|
C | T | 194 | a0002c0002t0001g0025a0002c0002t0001g0227a0002c0002t0001g0228others(191): Show | 195 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.437-47C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121162377 | ||||||
| chr12:121162416
|
C | T | 2 | a0021c0021t0001g0033a0021c0021t0001g0039 | 2 | HG02523.hp1 NA18747.hp2 |
splice_region_variant&intron_variant | LOW | c.437-8C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 4/12 | chr12 | 121162416 | ||||||
| chr12:121162559
|
G | A | 1 | a0018c0034t0005g0258 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.533+39G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162559 | ||||||
| chr12:121162578
|
G | C | 4 | a0002c0002t0036g0056a0007c0008t0001g0016a0007c0008t0001g0017others(1): Show | 4 | HG02280.hp1 HG02559.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+58G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162578 | ||||||
| chr12:121162662
|
T | G | 5 | a0012c0013t0005g0009a0012c0013t0005g0020a0012c0013t0005g0107others(2): Show | 5 | HG01069.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+142T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162662 | ||||||
| chr12:121162701
|
T | C | 1 | a0003c0004t0001g0122 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.533+181T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162701 | ||||||
| chr12:121162726
|
C | A | 153 | a0001c0001t0001g0052a0001c0001t0001g0098a0001c0001t0017g0077others(150): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.533+206C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162726 | ||||||
| chr12:121162887
|
A | G | 5 | a0007c0008t0001g0017a0017c0020t0002g0322a0017c0020t0002g0335others(2): Show | 5 | HG02965.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+367A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162887 | ||||||
| chr12:121162889
|
G | A | 1 | a0028c0040t0003g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.533+369G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162889 | ||||||
| chr12:121162924
|
G | A | 18 | a0009c0009t0006g0266a0009c0009t0006g0269a0009c0009t0006g0270others(15): Show | 18 | HG01943.hp1 HG04204.hp1 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.533+404G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162924 | ||||||
| chr12:121162928
|
A | G | 12 | a0001c0001t0001g0091a0004c0003t0007g0248a0004c0003t0007g0249others(9): Show | 12 | HG01243.hp1 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+408A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162928 | ||||||
| chr12:121162935
|
A | G | 19 | a0002c0002t0001g0227a0003c0004t0001g0094a0004c0003t0004g0219others(16): Show | 19 | HG00099.hp2 HG00621.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.533+415A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162935 | ||||||
| chr12:121162975
|
GA | G | 4 | a0002c0002t0003g0198a0004c0003t0007g0251a0004c0003t0012g0201others(1): Show | 4 | HG02818.hp1 NA18522.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+456delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162975 | ||||||
| chr12:121162976
|
A | G | 40 | a0001c0001t0001g0091a0001c0001t0034g0111a0002c0002t0003g0207others(37): Show | 40 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.533+456A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162976 | ||||||
| chr12:121162976
|
AG | A | 11 | a0011c0011t0004g0181a0011c0011t0004g0184a0011c0011t0004g0247others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.533+463delG | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121162976 | |||||
| chr12:121162983
|
G | A | 17 | a0001c0001t0001g0091a0004c0003t0012g0199a0004c0003t0012g0205others(14): Show | 17 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.533+463G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162983 | ||||||
| chr12:121162983
|
G | GA | 9 | a0004c0003t0004g0220a0004c0003t0004g0233a0004c0003t0007g0257others(6): Show | 9 | HG00099.hp2 HG02970.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.533+465dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121162983 | |||||
| chr12:121162999
|
G | A | 64 | a0001c0001t0001g0091a0002c0002t0001g0243a0002c0002t0001g0295others(61): Show | 65 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.533+479G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121162999 | ||||||
| chr12:121163008
|
C | G | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | HG01074.hp2 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.533+488C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163008 | ||||||
| chr12:121163150
|
G | A | 93 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0096others(90): Show | 95 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.533+630G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163150 | ||||||
| chr12:121163169
|
G | A | 1 | a0002c0002t0001g0295 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.533+649G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163169 | ||||||
| chr12:121163218
|
C | T | 22 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(19): Show | 22 | HG01943.hp1 HG02132.hp2 HG04204.hp1 others(19): Show |
intron_variant | MODIFIER | c.533+698C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163218 | ||||||
| chr12:121163253
|
T | C | 1 | a0003c0004t0001g0119 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.533+733T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163253 | ||||||
| chr12:121163327
|
T | TAC | 28 | a0002c0002t0001g0228a0002c0002t0001g0243a0002c0002t0003g0198others(25): Show | 28 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.533+836_533+837dup others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163327 | |||||
| chr12:121163327
|
T | TACAC | 7 | a0001c0001t0001g0331a0004c0003t0012g0199a0004c0003t0012g0201others(4): Show | 7 | HG00140.hp1 HG00280.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.533+834_533+837dup others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163327 | |||||
| chr12:121163327
|
TACAC | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0034others(9): Show | 12 | HG00423.hp1 HG01975.hp2 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.533+834_533+837del others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163327 | |||||
| chr12:121163332
|
A | ACAC | 5 | a0004c0003t0010g0299a0004c0003t0010g0300a0004c0003t0010g0301others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+813_533+815dup others(3): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163332 | |||||
| chr12:121163350
|
A | ACACACG | 3 | a0005c0006t0003g0358a0005c0006t0009g0192a0005c0006t0009g0193 | 3 | HG02145.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.533+835_533+836ins others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163350 | |||||
| chr12:121163354
|
A | ACACACAC others(3): Show |
1 | a0029c0037t0001g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.533+837_533+838ins others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163354 | |||||
| chr12:121163354
|
A | ACACACAC others(1): Show |
3 | a0011c0011t0005g0177a0015c0012t0012g0105a0024c0027t0005g0180 | 3 | HG02080.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.533+837_533+838ins others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163354 | |||||
| chr12:121163354
|
A | ACACACG | 5 | a0004c0003t0032g0200a0005c0006t0001g0339a0011c0011t0005g0178others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.533+837_533+838ins others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163354 | |||||
| chr12:121163354
|
A | ACG | 18 | a0002c0002t0003g0298a0002c0002t0003g0302a0002c0002t0003g0317others(15): Show | 18 | HG01168.hp2 HG01169.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.533+835_533+836ins others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163354 | |||||
| chr12:121163354
|
A | G | 71 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0076others(68): Show | 73 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.533+834A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163354 | ||||||
| chr12:121163356
|
A | ACACACAC others(5): Show |
1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.533+837_533+838ins others(12): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163356 | |||||
| chr12:121163356
|
A | ACACACG | 15 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(12): Show | 16 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+837_533+838ins others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163356 | |||||
| chr12:121163356
|
A | G | 37 | a0002c0002t0001g0171a0002c0002t0003g0207a0002c0002t0003g0208others(34): Show | 37 | HG01069.hp2 HG01243.hp2 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.533+836A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163356 | ||||||
| chr12:121163356
|
ACG | A | 66 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0076others(63): Show | 68 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.533+838_533+839del others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163356 | |||||
| chr12:121163358
|
G | A | 89 | a0002c0002t0001g0171a0002c0002t0001g0292a0002c0002t0003g0185others(86): Show | 90 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.533+838G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163358 | ||||||
| chr12:121163358
|
G | GCA | 27 | a0004c0003t0004g0226a0004c0003t0004g0240a0005c0006t0003g0358others(24): Show | 27 | HG01123.hp1 HG01943.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.533+857_533+858dup others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163358 | |||||
| chr12:121163358
|
G | GCACA | 7 | a0005c0006t0001g0289a0005c0006t0001g0291a0005c0006t0001g0310others(4): Show | 7 | NA18953.hp2 NA18957.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.533+855_533+858dup others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163358 | |||||
| chr12:121163358
|
G | GCACACAC others(3): Show |
1 | a0028c0040t0003g0066 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.533+845_533+846ins others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163358 | |||||
| chr12:121163360
|
A | G | 1 | a0014c0014t0003g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.533+840A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163360 | ||||||
| chr12:121163372
|
A | G | 67 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0076others(64): Show | 69 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.533+852A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163372 | ||||||
| chr12:121163431
|
G | A | 1 | a0010c0010t0006g0260 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.533+911G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163431 | ||||||
| chr12:121163496
|
A | G | 4 | a0007c0008t0001g0010a0007c0008t0001g0051a0007c0008t0001g0078others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.533+976A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163496 | ||||||
| chr12:121163505
|
A | G | 38 | a0002c0002t0003g0185a0004c0003t0010g0299a0004c0003t0010g0300others(35): Show | 39 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.533+985A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163505 | ||||||
| chr12:121163555
|
AAGAT | A | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | HG01943.hp1 HG02132.hp2 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.533+1049_533+1052d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163555 | |||||
| chr12:121163573
|
A | AATAG | 22 | a0002c0002t0001g0228a0004c0003t0004g0206a0004c0003t0004g0219others(19): Show | 22 | HG00558.hp1 HG01074.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.533+1057_533+1060d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163573 | |||||
| chr12:121163573
|
AATAGATA others(24): Show |
A | 102 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0103others(99): Show | 104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.533+1061_533+1091d others(33): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163573 | |||||
| chr12:121163577
|
GATA | G | 20 | a0002c0002t0001g0243a0004c0003t0004g0220a0004c0003t0004g0234others(17): Show | 20 | HG00621.hp1 HG01069.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.533+1061_533+1063d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163577 | |||||
| chr12:121163587
|
AG | A | 20 | a0002c0002t0001g0243a0004c0003t0004g0220a0004c0003t0004g0234others(17): Show | 20 | HG00621.hp1 HG01069.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.533+1068delG | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163587 | ||||||
| chr12:121163593
|
ACAGG | A | 4 | a0012c0013t0005g0006a0012c0013t0005g0087a0012c0013t0005g0147others(1): Show | 4 | HG02004.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+1074_533+1077d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163593 | ||||||
| chr12:121163594
|
C | T | 16 | a0002c0002t0001g0243a0004c0003t0004g0220a0004c0003t0004g0234others(13): Show | 16 | HG00621.hp1 HG01069.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1074C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163594 | ||||||
| chr12:121163597
|
G | A | 17 | a0002c0002t0001g0243a0004c0003t0004g0220a0004c0003t0004g0233others(14): Show | 17 | HG00099.hp2 HG00621.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.533+1077G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163597 | ||||||
| chr12:121163597
|
G | GTAGA | 3 | a0001c0001t0001g0034a0001c0001t0001g0098a0004c0003t0004g0226 | 3 | HG02895.hp2 NA18967.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.533+1126_533+1129d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163597
|
GTAGA | G | 76 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0027others(73): Show | 76 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.533+1126_533+1129d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163597
|
GTAGATAG others(1): Show |
G | 95 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0042others(92): Show | 96 | HG00323.hp2 HG00438.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.533+1122_533+1129d others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163597
|
GTAGATAG others(5): Show |
G | 22 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0043t0001g0089others(19): Show | 22 | HG00323.hp1 HG00741.hp2 HG02129.hp2 others(19): Show |
intron_variant | MODIFIER | c.533+1118_533+1129d others(14): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163597
|
GTAGATAG others(9): Show |
G | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.533+1114_533+1129d others(18): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163597
|
GTAGATAG others(13): Show |
G | 8 | a0007c0008t0001g0325a0013c0018t0004g0028a0013c0018t0004g0029others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.533+1110_533+1129d others(22): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163597
|
GTAGATAG others(21): Show |
G | 1 | a0013c0019t0004g0355 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.533+1102_533+1129d others(30): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163597
|
GTAGATAG others(29): Show |
G | 1 | a0025c0029t0003g0282 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.533+1094_533+1129d others(38): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 121163597 | |||||
| chr12:121163602
|
T | C | 16 | a0002c0002t0001g0243a0004c0003t0004g0220a0004c0003t0004g0234others(13): Show | 16 | HG00621.hp1 HG01069.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1082T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163602 | ||||||
| chr12:121163605
|
A | G | 16 | a0002c0002t0001g0243a0004c0003t0004g0220a0004c0003t0004g0234others(13): Show | 16 | HG00621.hp1 HG01069.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.533+1085A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163605 | ||||||
| chr12:121163606
|
T | C | 4 | a0012c0013t0005g0006a0012c0013t0005g0087a0012c0013t0005g0147others(1): Show | 4 | HG02004.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+1086T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163606 | ||||||
| chr12:121163609
|
A | G | 4 | a0012c0013t0005g0006a0012c0013t0005g0087a0012c0013t0005g0147others(1): Show | 4 | HG02004.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.533+1089A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163609 | ||||||
| chr12:121163610
|
T | C | 1 | a0004c0003t0004g0233 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.533+1090T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163610 | ||||||
| chr12:121163613
|
A | G | 1 | a0004c0003t0004g0233 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.533+1093A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163613 | ||||||
| chr12:121163615
|
AG | A | 102 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0103others(99): Show | 104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.533+1096delG | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163615 | ||||||
| chr12:121163630
|
T | C | 103 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0103others(100): Show | 105 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.533+1110T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163630 | ||||||
| chr12:121163633
|
A | G | 103 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0103others(100): Show | 105 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.533+1113A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163633 | ||||||
| chr12:121163652
|
T | C | 107 | a0001c0001t0001g0052a0001c0001t0001g0076a0001c0001t0001g0103others(104): Show | 109 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.533+1132T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163652 | ||||||
| chr12:121163663
|
G | C | 1 | a0010c0010t0006g0263 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.533+1143G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163663 | ||||||
| chr12:121163866
|
G | A | 1 | a0008c0039t0028g0012 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.533+1346G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163866 | ||||||
| chr12:121163945
|
C | T | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | HG01943.hp1 HG02132.hp2 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.534-1412C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163945 | ||||||
| chr12:121163986
|
G | C | 1 | a0005c0006t0001g0352 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.534-1371G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121163986 | ||||||
| chr12:121164026
|
GTCACAGA others(1): Show |
G | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-1330_534-1323d others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164026 | ||||||
| chr12:121164057
|
T | C | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.534-1300T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164057 | ||||||
| chr12:121164090
|
A | C | 4 | a0005c0006t0003g0358a0005c0006t0009g0192a0005c0006t0009g0193others(1): Show | 4 | HG00280.hp2 HG02145.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.534-1267A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164090 | ||||||
| chr12:121164198
|
G | C | 1 | a0029c0037t0001g0306 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.534-1159G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164198 | ||||||
| chr12:121164224
|
C | T | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.534-1133C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164224 | ||||||
| chr12:121164328
|
G | C | 1 | a0031c0036t0002g0225 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.534-1029G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164328 | ||||||
| chr12:121164332
|
C | A | 52 | a0001c0001t0001g0052a0001c0001t0001g0076a0002c0002t0001g0025others(49): Show | 54 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.534-1025C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164332 | ||||||
| chr12:121164435
|
G | A | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-922G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164435 | ||||||
| chr12:121164578
|
C | T | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-779C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164578 | ||||||
| chr12:121164602
|
G | A | 1 | a0033c0041t0001g0126 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.534-755G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164602 | ||||||
| chr12:121164617
|
C | T | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-740C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164617 | ||||||
| chr12:121164666
|
C | T | 27 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(24): Show | 27 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.534-691C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164666 | ||||||
| chr12:121164712
|
G | A | 27 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(24): Show | 27 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.534-645G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164712 | ||||||
| chr12:121164731
|
A | G | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-626A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164731 | ||||||
| chr12:121164825
|
T | C | 27 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(24): Show | 27 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.534-532T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164825 | ||||||
| chr12:121164832
|
C | T | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | HG01943.hp1 HG02132.hp2 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.534-525C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164832 | ||||||
| chr12:121164860
|
A | G | 1 | a0010c0010t0011g0280 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.534-497A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164860 | ||||||
| chr12:121164957
|
G | A | 63 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(60): Show | 63 | HG00280.hp2 HG01069.hp2 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.534-400G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164957 | ||||||
| chr12:121164998
|
T | C | 1 | a0033c0041t0001g0126 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.534-359T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121164998 | ||||||
| chr12:121165022
|
A | G | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-335A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121165022 | ||||||
| chr12:121165085
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.534-272G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121165085 | ||||||
| chr12:121165250
|
T | C | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-107T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121165250 | ||||||
| chr12:121165315
|
T | C | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-42T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121165315 | ||||||
| chr12:121165319
|
C | A | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.534-38C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 5/12 | chr12 | 121165319 | ||||||
| chr12:121165491
|
T | C | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | HG01943.hp1 HG02132.hp2 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.614+54T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | chr12 | 121165491 | ||||||
| chr12:121165666
|
A | C | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.614+229A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | chr12 | 121165666 | ||||||
| chr12:121165915
|
C | T | 2 | a0005c0006t0009g0192a0005c0006t0009g0193 | 2 | HG02145.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.615-143C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | chr12 | 121165915 | ||||||
| chr12:121165942
|
T | G | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.615-116T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | chr12 | 121165942 | ||||||
| chr12:121165966
|
C | A | 2 | a0034c0046t0002g0297a0035c0045t0022g0287 | 2 | NA18940.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.615-92C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | chr12 | 121165966 | ||||||
| chr12:121166005
|
A | T | 7 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.615-53A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | chr12 | 121166005 | ||||||
| chr12:121166022
|
ATGTT | A | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.615-21_615-18delTT others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 121166022 | |||||
| chr12:121166053
|
C | G | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
splice_region_variant&intron_variant | LOW | c.615-5C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 6/12 | chr12 | 121166053 | ||||||
| chr12:121166319
|
C | T | 3 | a0002c0002t0001g0079a0002c0002t0001g0118a0002c0002t0001g0171 | 3 | HG01074.hp1 HG01256.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.744+132C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166319 | ||||||
| chr12:121166323
|
A | G | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+136A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166323 | ||||||
| chr12:121166332
|
A | T | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+145A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166332 | ||||||
| chr12:121166343
|
C | G | 192 | a0001c0001t0001g0052a0001c0001t0001g0076a0002c0002t0001g0025others(189): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.744+156C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166343 | ||||||
| chr12:121166344
|
A | C | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+157A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166344 | ||||||
| chr12:121166447
|
G | C | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+260G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166447 | ||||||
| chr12:121166449
|
A | G | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | HG01943.hp1 HG02132.hp2 NA18945.hp2 others(18): Show |
intron_variant | MODIFIER | c.744+262A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166449 | ||||||
| chr12:121166511
|
A | G | 90 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(87): Show | 90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.744+324A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166511 | ||||||
| chr12:121166522
|
C | T | 27 | a0002c0002t0001g0228a0002c0002t0001g0243a0004c0003t0004g0206others(24): Show | 27 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.744+335C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166522 | ||||||
| chr12:121166673
|
C | A | 26 | a0002c0002t0001g0243a0004c0003t0004g0206a0004c0003t0004g0219others(23): Show | 26 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.744+486C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166673 | ||||||
| chr12:121166887
|
C | CA | 10 | a0001c0001t0001g0057a0001c0001t0001g0331a0002c0002t0001g0333others(7): Show | 10 | HG00140.hp1 HG01243.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.745-585dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 121166887 | |||||
| chr12:121166887
|
C | CAA | 20 | a0004c0003t0004g0219a0004c0003t0004g0220a0004c0003t0004g0221others(17): Show | 20 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.745-586_745-585dup others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 121166887 | |||||
| chr12:121166887
|
C | CAAA | 8 | a0004c0003t0004g0206a0013c0018t0004g0028a0013c0018t0004g0029others(5): Show | 8 | HG01243.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.745-587_745-585dup others(3): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 121166887 | |||||
| chr12:121166887
|
CA | C | 19 | a0001c0001t0001g0090a0004c0003t0007g0248a0004c0003t0007g0249others(16): Show | 19 | HG00099.hp1 HG00280.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.745-585delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 121166887 | |||||
| chr12:121166921
|
A | G | 36 | a0002c0002t0001g0243a0004c0003t0004g0206a0004c0003t0004g0219others(33): Show | 36 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.745-567A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166921 | ||||||
| chr12:121166945
|
G | A | 105 | a0001c0001t0001g0052a0001c0001t0001g0076a0002c0002t0001g0025others(102): Show | 107 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.745-543G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121166945 | ||||||
| chr12:121167013
|
C | T | 1 | a0003c0004t0001g0093 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.745-475C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121167013 | ||||||
| chr12:121167052
|
C | CA | 32 | a0001c0001t0001g0052a0001c0001t0001g0141a0002c0002t0001g0295others(29): Show | 32 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.745-419dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 121167052 | |||||
| chr12:121167052
|
CA | C | 43 | a0002c0002t0001g0243a0002c0002t0003g0302a0004c0003t0008g0238others(40): Show | 43 | HG00280.hp2 HG01243.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.745-419delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 121167052 | |||||
| chr12:121167052
|
CAA | C | 26 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(23): Show | 26 | HG00741.hp1 HG01069.hp2 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.745-420_745-419del others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 121167052 | |||||
| chr12:121167147
|
A | G | 9 | a0013c0018t0004g0028a0013c0018t0004g0029a0013c0018t0004g0175others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.745-341A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121167147 | ||||||
| chr12:121167271
|
G | A | 99 | a0002c0002t0001g0079a0002c0002t0001g0118a0002c0002t0001g0171others(96): Show | 100 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.745-217G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121167271 | ||||||
| chr12:121167292
|
G | A | 8 | a0013c0018t0004g0028a0013c0018t0004g0029a0013c0018t0004g0175others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.745-196G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121167292 | ||||||
| chr12:121167386
|
C | T | 98 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.745-102C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 7/12 | chr12 | 121167386 | ||||||
| chr12:121167705
|
A | G | 1 | a0010c0010t0025g0281 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.881+81A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121167705 | ||||||
| chr12:121167771
|
T | C | 1 | a0010c0010t0006g0261 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.881+147T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121167771 | ||||||
| chr12:121167787
|
A | G | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.881+163A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121167787 | ||||||
| chr12:121167796
|
C | T | 107 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(104): Show | 108 | HG00099.hp2 HG00621.hp1 HG01069.hp2 others(105): Show |
intron_variant | MODIFIER | c.881+172C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121167796 | ||||||
| chr12:121167806
|
A | AT | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+188dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121167806 | |||||
| chr12:121167814
|
CTTA | C | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.881+193_881+195del others(3): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121167814 | |||||
| chr12:121167817
|
A | AT | 8 | a0004c0003t0004g0226a0004c0003t0004g0232a0004c0003t0010g0299others(5): Show | 8 | HG01891.hp1 HG02015.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.881+206dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121167817 | |||||
| chr12:121167847
|
CTG | C | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.881+225_881+226del others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121167847 | |||||
| chr12:121167899
|
G | A | 1 | a0002c0024t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.881+275G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121167899 | ||||||
| chr12:121167953
|
T | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+329T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121167953 | ||||||
| chr12:121168023
|
A | G | 28 | a0004c0003t0008g0238a0004c0003t0008g0239a0004c0003t0008g0241others(25): Show | 28 | HG01943.hp1 HG02165.hp2 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.881+399A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168023 | ||||||
| chr12:121168042
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+418T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168042 | ||||||
| chr12:121168064
|
C | T | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.881+440C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168064 | ||||||
| chr12:121168116
|
A | C | 175 | a0002c0002t0035g0343a0004c0003t0004g0206a0004c0003t0004g0219others(172): Show | 176 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.881+492A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168116 | ||||||
| chr12:121168121
|
C | CAT | 46 | a0002c0002t0001g0227a0002c0002t0001g0228a0002c0002t0001g0285others(43): Show | 46 | HG00558.hp1 HG01943.hp1 HG02129.hp1 others(43): Show |
intron_variant | MODIFIER | c.881+510_881+511dup others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121168121 | |||||
| chr12:121168151
|
G | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+527G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168151 | ||||||
| chr12:121168202
|
T | C | 9 | a0013c0018t0004g0028a0013c0018t0004g0029a0013c0018t0004g0175others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.881+578T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168202 | ||||||
| chr12:121168256
|
C | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+632C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168256 | ||||||
| chr12:121168260
|
G | GTTTTC | 76 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(73): Show | 76 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.881+656_881+660dup others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121168260 | |||||
| chr12:121168260
|
G | GTTTTCTT others(3): Show |
3 | a0019c0022t0005g0196a0019c0022t0005g0244a0019c0022t0005g0308 | 3 | HG02896.hp2 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.881+651_881+660dup others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121168260 | |||||
| chr12:121168260
|
G | GTTTTCTT others(13): Show |
10 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(7): Show | 11 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.881+641_881+660dup others(20): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121168260 | |||||
| chr12:121168280
|
C | CTTTTCT | 22 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(19): Show | 22 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.881+660_881+661ins others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121168280 | |||||
| chr12:121168386
|
C | T | 1 | a0019c0022t0005g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.881+762C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168386 | ||||||
| chr12:121168516
|
G | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+892G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168516 | ||||||
| chr12:121168547
|
G | T | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+923G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168547 | ||||||
| chr12:121168602
|
G | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+978G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168602 | ||||||
| chr12:121168782
|
G | A | 1 | a0006c0005t0002g0164 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.881+1158G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168782 | ||||||
| chr12:121168818
|
C | T | 1 | a0002c0024t0001g0283 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.881+1194C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168818 | ||||||
| chr12:121168844
|
A | C | 7 | a0002c0002t0003g0207a0002c0002t0003g0208a0002c0002t0003g0209others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+1220A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168844 | ||||||
| chr12:121168957
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+1333A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121168957 | ||||||
| chr12:121169044
|
C | A | 1 | a0002c0002t0033g0294 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.881+1420C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169044 | ||||||
| chr12:121169087
|
T | C | 2 | a0022c0025t0015g0195a0022c0025t0015g0204 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.881+1463T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169087 | ||||||
| chr12:121169114
|
C | T | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+1490C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169114 | ||||||
| chr12:121169209
|
C | T | 1 | a0015c0012t0006g0154 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.881+1585C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169209 | ||||||
| chr12:121169210
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.881+1586G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169210 | ||||||
| chr12:121169249
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+1625A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169249 | ||||||
| chr12:121169253
|
C | T | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.881+1629C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169253 | ||||||
| chr12:121169537
|
C | T | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+1913C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169537 | ||||||
| chr12:121169541
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+1917A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169541 | ||||||
| chr12:121169660
|
C | T | 1 | a0004c0003t0027g0309 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.881+2036C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169660 | ||||||
| chr12:121169844
|
G | T | 354 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(351): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.881+2220G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169844 | ||||||
| chr12:121169881
|
C | T | 1 | a0024c0027t0021g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.881+2257C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169881 | ||||||
| chr12:121169992
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+2368A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121169992 | ||||||
| chr12:121170058
|
G | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+2434G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170058 | ||||||
| chr12:121170087
|
C | T | 1 | a0025c0029t0003g0282 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.881+2463C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170087 | ||||||
| chr12:121170088
|
G | A | 118 | a0001c0001t0001g0159a0002c0002t0001g0079a0002c0002t0001g0118others(115): Show | 120 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.881+2464G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170088 | ||||||
| chr12:121170177
|
C | T | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0096 | 3 | NA18994.hp1 NA19003.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.881+2553C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170177 | ||||||
| chr12:121170184
|
G | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+2560G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170184 | ||||||
| chr12:121170215
|
A | C | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.881+2591A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170215 | ||||||
| chr12:121170224
|
A | G | 1 | a0002c0002t0003g0298 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.881+2600A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170224 | ||||||
| chr12:121170306
|
C | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0110a0001c0001t0001g0150others(2): Show | 5 | HG02071.hp2 NA18953.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.881+2682C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170306 | ||||||
| chr12:121170332
|
G | A | 5 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(2): Show | 5 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.881+2708G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170332 | ||||||
| chr12:121170470
|
C | T | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+2846C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170470 | ||||||
| chr12:121170513
|
G | A | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+2889G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170513 | ||||||
| chr12:121170514
|
C | G | 10 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(7): Show | 11 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.881+2890C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170514 | ||||||
| chr12:121170572
|
C | T | 1 | a0002c0002t0001g0228 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.881+2948C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170572 | ||||||
| chr12:121170639
|
G | A | 7 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+3015G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170639 | ||||||
| chr12:121170753
|
G | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+3129G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170753 | ||||||
| chr12:121170782
|
A | T | 31 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.881+3158A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170782 | ||||||
| chr12:121170823
|
T | C | 1 | a0016c0016t0002g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.881+3199T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170823 | ||||||
| chr12:121170860
|
G | C | 7 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.881+3236G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170860 | ||||||
| chr12:121170877
|
C | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.881+3253C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170877 | ||||||
| chr12:121170972
|
G | A | 53 | a0006c0005t0002g0013a0006c0005t0002g0032a0006c0005t0002g0043others(50): Show | 53 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.881+3348G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121170972 | ||||||
| chr12:121171019
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.881+3395G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171019 | ||||||
| chr12:121171053
|
C | T | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.881+3429C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171053 | ||||||
| chr12:121171055
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0169 | 2 | HG01123.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.881+3431C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171055 | ||||||
| chr12:121171105
|
G | A | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.881+3481G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171105 | ||||||
| chr12:121171320
|
C | T | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.881+3696C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171320 | ||||||
| chr12:121171359
|
C | CT | 60 | a0001c0001t0001g0042a0001c0001t0001g0052a0002c0002t0001g0227others(57): Show | 60 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.881+3757dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171359 | |||||
| chr12:121171359
|
CT | C | 39 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(36): Show | 40 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.881+3757delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171359 | |||||
| chr12:121171359
|
CTT | C | 61 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(58): Show | 61 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.881+3756_881+3757d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171359 | |||||
| chr12:121171426
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.881+3802G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171426 | ||||||
| chr12:121171585
|
T | G | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-3803T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171585 | ||||||
| chr12:121171691
|
C | T | 31 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.882-3697C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171691 | ||||||
| chr12:121171729
|
C | T | 1 | a0002c0002t0035g0343 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.882-3659C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171729 | ||||||
| chr12:121171805
|
A | G | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.882-3583A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171805 | ||||||
| chr12:121171851
|
A | ATTCT | 44 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(41): Show | 44 | HG00099.hp2 HG00621.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.882-3526_882-3523d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171851 | |||||
| chr12:121171862
|
C | CT | 7 | a0002c0002t0001g0286a0002c0002t0003g0208a0003c0004t0001g0156others(4): Show | 7 | HG00323.hp2 HG00423.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.882-3509dupT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171862 | |||||
| chr12:121171862
|
C | CTTTCT | 27 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(24): Show | 27 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.882-3523_882-3522i others(7): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171862 | |||||
| chr12:121171862
|
C | CTTTCTT | 10 | a0004c0003t0008g0238a0004c0003t0008g0239a0004c0003t0008g0241others(7): Show | 10 | HG01943.hp1 HG02165.hp2 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.882-3523_882-3522i others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171862 | |||||
| chr12:121171862
|
C | CTTTCTTT | 18 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(15): Show | 18 | NA18945.hp2 NA18947.hp1 NA18950.hp2 others(15): Show |
intron_variant | MODIFIER | c.882-3523_882-3522i others(9): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171862 | |||||
| chr12:121171862
|
CT | C | 14 | a0002c0002t0001g0130a0011c0011t0004g0181a0011c0011t0004g0182others(11): Show | 15 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.882-3509delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121171862 | |||||
| chr12:121171930
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0067others(4): Show | 7 | HG00140.hp1 HG01099.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.882-3458C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121171930 | ||||||
| chr12:121172010
|
C | T | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.882-3378C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172010 | ||||||
| chr12:121172102
|
CTGCCTGC others(15): Show |
C | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.882-3282_882-3261d others(24): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121172102 | |||||
| chr12:121172140
|
C | T | 6 | a0008c0007t0002g0237a0008c0007t0002g0305a0008c0007t0002g0314others(3): Show | 6 | HG00621.hp2 HG02080.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.882-3248C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172140 | ||||||
| chr12:121172141
|
G | A | 95 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.882-3247G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172141 | ||||||
| chr12:121172150
|
T | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.882-3238T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172150 | ||||||
| chr12:121172152
|
C | T | 1 | a0004c0003t0020g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.882-3236C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172152 | ||||||
| chr12:121172232
|
G | C | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-3156G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172232 | ||||||
| chr12:121172358
|
G | A | 3 | a0012c0013t0005g0009a0012c0013t0005g0020a0012c0013t0005g0107 | 3 | HG01069.hp2 HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.882-3030G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172358 | ||||||
| chr12:121172489
|
G | A | 1 | a0024c0027t0021g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882-2899G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172489 | ||||||
| chr12:121172563
|
G | A | 1 | a0024c0027t0021g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.882-2825G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172563 | ||||||
| chr12:121172608
|
A | G | 325 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(322): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.882-2780A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172608 | ||||||
| chr12:121172643
|
A | C | 1 | a0004c0003t0004g0223 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.882-2745A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172643 | ||||||
| chr12:121172686
|
A | G | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.882-2702A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172686 | ||||||
| chr12:121172884
|
G | C | 7 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.882-2504G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172884 | ||||||
| chr12:121172952
|
CA | C | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.882-2435delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121172952 | ||||||
| chr12:121173081
|
T | C | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-2307T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173081 | ||||||
| chr12:121173157
|
C | A | 1 | a0003c0004t0001g0003 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.882-2231C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173157 | ||||||
| chr12:121173167
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.882-2221C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173167 | ||||||
| chr12:121173176
|
T | TTTTG | 70 | a0002c0024t0001g0283a0004c0003t0007g0248a0004c0003t0007g0249others(67): Show | 70 | HG01069.hp2 HG01243.hp2 HG01517.hp2 others(67): Show |
intron_variant | MODIFIER | c.882-2187_882-2184d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121173176 | |||||
| chr12:121173176
|
TTTTG | T | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-2187_882-2184d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121173176 | |||||
| chr12:121173252
|
A | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.882-2136A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173252 | ||||||
| chr12:121173331
|
G | A | 3 | a0006c0005t0002g0099a0006c0005t0002g0100a0006c0005t0002g0106 | 3 | HG01981.hp1 HG01993.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.882-2057G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173331 | ||||||
| chr12:121173398
|
T | C | 171 | a0002c0002t0035g0343a0004c0003t0004g0206a0004c0003t0004g0219others(168): Show | 172 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.882-1990T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173398 | ||||||
| chr12:121173478
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.882-1910A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173478 | ||||||
| chr12:121173547
|
T | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.882-1841T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173547 | ||||||
| chr12:121173688
|
G | A | 2 | a0011c0011t0004g0184a0011c0011t0004g0247 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.882-1700G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173688 | ||||||
| chr12:121173735
|
G | T | 1 | a0002c0002t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.882-1653G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173735 | ||||||
| chr12:121173832
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.882-1556A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121173832 | ||||||
| chr12:121174045
|
TTTC | T | 18 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(15): Show | 18 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.882-1340_882-1338d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121174045 | |||||
| chr12:121174046
|
TTC | T | 33 | a0004c0003t0004g0222a0004c0003t0008g0238a0004c0003t0008g0239others(30): Show | 33 | HG01069.hp2 HG01074.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.882-1340_882-1339d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121174046 | |||||
| chr12:121174047
|
TC | T | 57 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(54): Show | 58 | HG00099.hp2 HG00621.hp1 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.882-1340delC | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174047 | ||||||
| chr12:121174048
|
C | T | 1 | a0011c0011t0004g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.882-1340C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174048 | ||||||
| chr12:121174048
|
CT | C | 123 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0014others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.882-1321delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121174048 | |||||
| chr12:121174048
|
CTT | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0034a0001c0001t0001g0132others(4): Show | 8 | HG02723.hp1 HG02895.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.882-1322_882-1321d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121174048 | |||||
| chr12:121174096
|
A | G | 1 | a0004c0003t0004g0219 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.882-1292A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174096 | ||||||
| chr12:121174100
|
C | T | 1 | a0005c0006t0001g0351 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.882-1288C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174100 | ||||||
| chr12:121174111
|
G | A | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-1277G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174111 | ||||||
| chr12:121174126
|
T | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.882-1262T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174126 | ||||||
| chr12:121174185
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-1203T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174185 | ||||||
| chr12:121174295
|
G | C | 4 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0243others(1): Show | 4 | HG00140.hp2 HG02698.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.882-1093G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174295 | ||||||
| chr12:121174344
|
G | A | 2 | a0006c0005t0013g0172a0006c0005t0013g0173 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.882-1044G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174344 | ||||||
| chr12:121174561
|
T | A | 46 | a0006c0005t0002g0013a0006c0005t0002g0032a0006c0005t0002g0043others(43): Show | 46 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.882-827T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174561 | ||||||
| chr12:121174562
|
T | C | 1 | a0002c0002t0003g0336 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.882-826T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174562 | ||||||
| chr12:121174563
|
G | T | 1 | a0002c0002t0003g0336 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.882-825G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174563 | ||||||
| chr12:121174565
|
C | G | 1 | a0002c0002t0003g0336 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.882-823C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174565 | ||||||
| chr12:121174588
|
T | C | 1 | a0004c0003t0010g0300 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.882-800T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174588 | ||||||
| chr12:121174640
|
C | A | 3 | a0002c0002t0035g0343a0005c0006t0001g0337a0005c0006t0001g0341 | 3 | HG01168.hp2 HG01169.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.882-748C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174640 | ||||||
| chr12:121174794
|
T | C | 3 | a0022c0025t0015g0195a0022c0025t0015g0204a0024c0027t0021g0197 | 3 | HG01891.hp2 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.882-594T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174794 | ||||||
| chr12:121174829
|
C | T | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-559C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174829 | ||||||
| chr12:121174843
|
G | T | 9 | a0013c0018t0004g0028a0013c0018t0004g0029a0013c0018t0004g0175others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.882-545G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174843 | ||||||
| chr12:121174858
|
G | A | 1 | a0004c0003t0004g0240 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.882-530G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121174858 | ||||||
| chr12:121175099
|
C | T | 1 | a0001c0001t0001g0331 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.882-289C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175099 | ||||||
| chr12:121175138
|
C | T | 61 | a0002c0002t0001g0025a0002c0002t0001g0227a0002c0002t0001g0228others(58): Show | 62 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.882-250C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175138 | ||||||
| chr12:121175173
|
C | T | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-215C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175173 | ||||||
| chr12:121175174
|
G | T | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-214G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175174 | ||||||
| chr12:121175175
|
G | T | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-213G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175175 | ||||||
| chr12:121175176
|
T | TTTGTACA | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-212_882-211ins others(7): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175176 | ||||||
| chr12:121175243
|
C | T | 39 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.882-145C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175243 | ||||||
| chr12:121175257
|
G | C | 55 | a0006c0005t0002g0013a0006c0005t0002g0032a0006c0005t0002g0043others(52): Show | 55 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.882-131G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175257 | ||||||
| chr12:121175287
|
G | A | 46 | a0006c0005t0002g0013a0006c0005t0002g0032a0006c0005t0002g0043others(43): Show | 46 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.882-101G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175287 | ||||||
| chr12:121175310
|
C | CA | 35 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0092others(32): Show | 36 | HG00140.hp1 HG00438.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.882-59dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA | 11 | a0005c0017t0005g0215a0005c0017t0005g0290a0012c0013t0005g0006others(8): Show | 11 | HG01069.hp2 HG01517.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-65_882-59dupAA others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA others(1): Show |
14 | a0004c0003t0008g0238a0004c0003t0008g0239a0004c0003t0008g0241others(11): Show | 14 | HG00735.hp2 HG01943.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-66_882-59dupAA others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA others(2): Show |
23 | a0004c0003t0004g0231a0004c0003t0008g0242a0004c0003t0010g0299others(20): Show | 23 | HG00280.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.882-67_882-59dupAA others(7): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA others(3): Show |
26 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(23): Show | 26 | HG00099.hp2 HG00642.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.882-68_882-59dupAA others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA others(4): Show |
15 | a0004c0003t0004g0221a0004c0003t0004g0223a0004c0003t0004g0226others(12): Show | 15 | HG00621.hp1 HG01168.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.882-69_882-59dupAA others(9): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA others(5): Show |
5 | a0004c0003t0007g0251a0004c0003t0007g0257a0004c0003t0007g0354others(2): Show | 5 | HG02970.hp2 HG03041.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.882-70_882-59dupAA others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA others(6): Show |
3 | a0004c0003t0004g0240a0004c0003t0007g0248a0004c0003t0007g0249 | 3 | HG01123.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.882-71_882-59dupAA others(11): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175310
|
C | CAAAAAAA others(8): Show |
1 | a0004c0003t0007g0250 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.882-73_882-59dupAA others(13): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175310 | |||||
| chr12:121175322
|
A | AAAAC | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-63_882-62insCA others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 121175322 | |||||
| chr12:121175341
|
G | C | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.882-47G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 8/12 | chr12 | 121175341 | ||||||
| chr12:121175632
|
G | A | 3 | a0002c0002t0035g0343a0005c0006t0001g0337a0005c0006t0001g0341 | 3 | HG01168.hp2 HG01169.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.972+154G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121175632 | ||||||
| chr12:121175632
|
G | C | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.972+154G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121175632 | ||||||
| chr12:121175686
|
C | A | 2 | a0013c0018t0004g0028a0013c0018t0004g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.972+208C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121175686 | ||||||
| chr12:121175798
|
G | GA | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.972+329dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121175798 | |||||
| chr12:121175800
|
A | T | 4 | a0002c0002t0001g0130a0002c0002t0001g0131a0002c0002t0001g0243others(1): Show | 4 | HG00140.hp2 HG02698.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+322A>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121175800 | ||||||
| chr12:121175802
|
A | G | 3 | a0007c0008t0001g0016a0007c0008t0001g0017a0007c0008t0001g0018 | 3 | HG02280.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.972+324A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121175802 | ||||||
| chr12:121175892
|
T | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.972+414T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121175892 | ||||||
| chr12:121176112
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.972+634C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176112 | ||||||
| chr12:121176228
|
A | AAC | 6 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0290others(3): Show | 6 | HG00280.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.972+791_972+792dup others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACAC | 11 | a0004c0003t0004g0234a0004c0003t0012g0199a0004c0003t0012g0201others(8): Show | 11 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.972+789_972+792dup others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACACAC | 8 | a0004c0003t0011g0133a0010c0010t0011g0278a0010c0010t0011g0279others(5): Show | 8 | HG01074.hp2 HG01168.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.972+787_972+792dup others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACACACA others(1): Show |
5 | a0004c0003t0004g0206a0004c0003t0004g0226a0004c0003t0004g0232others(2): Show | 5 | HG00099.hp2 HG02155.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.972+785_972+792dup others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACACACA others(3): Show |
9 | a0004c0003t0004g0219a0004c0003t0004g0220a0004c0003t0004g0222others(6): Show | 9 | HG02071.hp1 HG02145.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.972+783_972+792dup others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACACACA others(5): Show |
10 | a0004c0003t0004g0221a0004c0003t0004g0223a0004c0003t0004g0229others(7): Show | 10 | HG01123.hp1 HG02165.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.972+781_972+792dup others(12): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACACACA others(7): Show |
4 | a0013c0018t0004g0188a0013c0019t0004g0190a0013c0019t0004g0191others(1): Show | 4 | HG02615.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.972+779_972+792dup others(14): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACACACA others(9): Show |
2 | a0004c0003t0008g0241a0010c0010t0025g0281 | 2 | HG01943.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.972+777_972+792dup others(16): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
A | AACACACA others(11): Show |
1 | a0004c0003t0008g0242 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.972+775_972+792dup others(18): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
AAC | A | 71 | a0001c0001t0001g0151a0001c0001t0001g0169a0001c0001t0017g0161others(68): Show | 73 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.972+791_972+792del others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
AACAC | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.972+789_972+792del others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
AACACAC | A | 3 | a0003c0004t0001g0084a0021c0021t0001g0033a0021c0021t0001g0039 | 3 | HG00558.hp2 HG02523.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.972+787_972+792del others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
AACACACA others(1): Show |
A | 14 | a0001c0001t0001g0090a0011c0011t0004g0181a0011c0011t0004g0182others(11): Show | 15 | HG00099.hp1 HG01099.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.972+785_972+792del others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
AACACACA others(5): Show |
A | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.972+781_972+792del others(12): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176228
|
AACACACA others(9): Show |
A | 4 | a0004c0003t0010g0299a0004c0003t0010g0300a0004c0003t0010g0301others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.972+777_972+792del others(16): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176228 | |||||
| chr12:121176390
|
G | C | 1 | a0004c0003t0007g0250 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.973-757G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176390 | ||||||
| chr12:121176424
|
T | C | 23 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(20): Show | 23 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.973-723T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176424 | ||||||
| chr12:121176445
|
C | T | 10 | a0012c0013t0005g0006a0012c0013t0005g0009a0012c0013t0005g0020others(7): Show | 10 | HG01069.hp2 HG01517.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.973-702C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176445 | ||||||
| chr12:121176481
|
G | A | 2 | a0012c0013t0005g0009a0012c0013t0005g0107 | 2 | HG01069.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.973-666G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176481 | ||||||
| chr12:121176521
|
G | A | 78 | a0002c0002t0001g0025a0002c0002t0001g0079a0002c0002t0001g0118others(75): Show | 80 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.973-626G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176521 | ||||||
| chr12:121176525
|
G | A | 1 | a0002c0002t0036g0056 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.973-622G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176525 | ||||||
| chr12:121176534
|
T | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.973-613T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176534 | ||||||
| chr12:121176535
|
G | A | 99 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.973-612G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176535 | ||||||
| chr12:121176549
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.973-598A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176549 | ||||||
| chr12:121176581
|
T | A | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.973-566T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176581 | ||||||
| chr12:121176617
|
C | T | 1 | a0002c0002t0003g0323 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.973-530C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176617 | ||||||
| chr12:121176731
|
A | G | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.973-416A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176731 | ||||||
| chr12:121176733
|
G | A | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.973-414G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176733 | ||||||
| chr12:121176751
|
C | CA | 55 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0052others(52): Show | 56 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.973-375dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176751 | |||||
| chr12:121176751
|
C | CAA | 27 | a0002c0024t0001g0283a0004c0003t0004g0206a0004c0003t0004g0219others(24): Show | 27 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.973-376_973-375dup others(2): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 121176751 | |||||
| chr12:121176874
|
G | T | 2 | a0008c0007t0002g0326a0008c0007t0002g0332 | 2 | HG00323.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.973-273G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121176874 | ||||||
| chr12:121177027
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0112a0001c0001t0001g0141 | 3 | NA18942.hp2 NA18968.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.973-120C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121177027 | ||||||
| chr12:121177131
|
C | T | 50 | a0006c0005t0002g0013a0006c0005t0002g0032a0006c0005t0002g0043others(47): Show | 50 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.973-16C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 9/12 | chr12 | 121177131 | ||||||
| chr12:121177480
|
T | C | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1188+34T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177480 | ||||||
| chr12:121177560
|
G | A | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+114G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177560 | ||||||
| chr12:121177566
|
T | C | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1188+120T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177566 | ||||||
| chr12:121177594
|
A | G | 2 | a0006c0005t0023g0071a0006c0005t0029g0007 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1188+148A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177594 | ||||||
| chr12:121177687
|
C | CATTT | 88 | a0001c0001t0001g0004a0001c0001t0001g0047a0001c0001t0001g0132others(85): Show | 89 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1188+286_1188+289d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121177687 | |||||
| chr12:121177687
|
C | CATTTATT others(1): Show |
3 | a0003c0004t0001g0113a0004c0003t0007g0248a0004c0003t0027g0309 | 3 | HG02165.hp2 HG02809.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.1188+282_1188+289d others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121177687 | |||||
| chr12:121177687
|
CATTT | C | 64 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0091others(61): Show | 65 | HG00621.hp2 HG00735.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.1188+286_1188+289d others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121177687 | |||||
| chr12:121177687
|
CATTTATT others(1): Show |
C | 9 | a0001c0043t0001g0089a0005c0017t0005g0214a0005c0017t0005g0215others(6): Show | 9 | HG02523.hp1 HG02818.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1188+282_1188+289d others(10): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121177687 | |||||
| chr12:121177687
|
CATTTATT others(5): Show |
C | 1 | a0032c0035t0002g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1188+278_1188+289d others(14): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121177687 | |||||
| chr12:121177687
|
CATTTATT others(9): Show |
C | 10 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(7): Show | 11 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1188+274_1188+289d others(18): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121177687 | |||||
| chr12:121177755
|
A | G | 2 | a0001c0001t0001g0095a0007c0008t0001g0357 | 2 | HG02129.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1188+309A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177755 | ||||||
| chr12:121177789
|
G | T | 1 | a0003c0004t0001g0119 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1188+343G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177789 | ||||||
| chr12:121177826
|
C | G | 12 | a0012c0013t0005g0006a0012c0013t0005g0009a0012c0013t0005g0020others(9): Show | 12 | HG01069.hp2 HG01517.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1188+380C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177826 | ||||||
| chr12:121177838
|
C | T | 32 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(29): Show | 33 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1188+392C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177838 | ||||||
| chr12:121177983
|
G | C | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1188+537G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121177983 | ||||||
| chr12:121178088
|
C | T | 1 | a0010c0010t0006g0265 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1188+642C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178088 | ||||||
| chr12:121178116
|
G | C | 1 | a0019c0022t0005g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1188+670G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178116 | ||||||
| chr12:121178193
|
A | G | 3 | a0022c0025t0015g0195a0022c0025t0015g0204a0024c0027t0021g0197 | 3 | HG01891.hp2 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1188+747A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178193 | ||||||
| chr12:121178378
|
T | C | 1 | a0002c0002t0001g0286 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1188+932T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178378 | ||||||
| chr12:121178529
|
C | T | 1 | a0022c0025t0015g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1188+1083C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178529 | ||||||
| chr12:121178589
|
C | T | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | NA18945.hp2 NA18946.hp1 NA18947.hp1 others(18): Show |
intron_variant | MODIFIER | c.1188+1143C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178589 | ||||||
| chr12:121178653
|
G | A | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1188+1207G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178653 | ||||||
| chr12:121178661
|
G | A | 23 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(20): Show | 23 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1188+1215G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178661 | ||||||
| chr12:121178664
|
T | C | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1188+1218T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178664 | ||||||
| chr12:121178791
|
C | CA | 34 | a0001c0001t0001g0014a0001c0001t0001g0058a0002c0002t0003g0298others(31): Show | 34 | HG01074.hp2 HG01169.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.1188+1367dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121178791 | |||||
| chr12:121178791
|
C | CAA | 50 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(47): Show | 50 | HG00099.hp2 HG00621.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.1188+1366_1188+136 others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121178791 | |||||
| chr12:121178791
|
C | CAAA | 20 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(17): Show | 20 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1188+1365_1188+136 others(7): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121178791 | |||||
| chr12:121178791
|
C | CAAAA | 12 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(9): Show | 13 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1188+1364_1188+136 others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121178791 | |||||
| chr12:121178791
|
CA | C | 17 | a0001c0001t0001g0140a0002c0002t0001g0118a0002c0002t0003g0256others(14): Show | 17 | HG01069.hp1 HG01074.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1188+1367delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121178791 | |||||
| chr12:121178819
|
GGACTT | G | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1188+1377_1188+138 others(9): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121178819 | |||||
| chr12:121178903
|
G | A | 1 | a0006c0005t0013g0173 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1189-1451G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178903 | ||||||
| chr12:121178922
|
G | C | 21 | a0009c0009t0006g0266a0009c0009t0006g0267a0009c0009t0006g0268others(18): Show | 21 | NA18945.hp2 NA18946.hp1 NA18947.hp1 others(18): Show |
intron_variant | MODIFIER | c.1189-1432G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178922 | ||||||
| chr12:121178966
|
T | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0132 | 3 | NA18957.hp2 NA18960.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1189-1388T>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121178966 | ||||||
| chr12:121178978
|
T | TAC | 9 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(6): Show | 10 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1189-1362_1189-136 others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121178978 | |||||
| chr12:121179093
|
G | T | 1 | a0008c0007t0002g0346 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1189-1261G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179093 | ||||||
| chr12:121179137
|
T | G | 5 | a0003c0004t0001g0003a0003c0004t0001g0015a0003c0004t0001g0026others(2): Show | 6 | HG01071.hp2 HG01255.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-1217T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179137 | ||||||
| chr12:121179183
|
G | A | 1 | a0006c0005t0013g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1189-1171G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179183 | ||||||
| chr12:121179455
|
G | A | 2 | a0018c0026t0016g0080a0018c0026t0016g0081 | 2 | HG03669.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1189-899G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179455 | ||||||
| chr12:121179457
|
G | A | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1189-897G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179457 | ||||||
| chr12:121179469
|
C | T | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1189-885C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179469 | ||||||
| chr12:121179500
|
C | CA | 11 | a0002c0002t0003g0217a0002c0002t0003g0252a0002c0002t0036g0056others(8): Show | 11 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189-838dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121179500 | |||||
| chr12:121179500
|
CA | C | 81 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(78): Show | 82 | HG00099.hp2 HG00621.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.1189-838delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121179500 | |||||
| chr12:121179575
|
C | G | 31 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(28): Show | 31 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1189-779C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179575 | ||||||
| chr12:121179583
|
T | C | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1189-771T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179583 | ||||||
| chr12:121179694
|
G | A | 6 | a0008c0007t0002g0237a0008c0007t0002g0305a0008c0007t0002g0314others(3): Show | 6 | HG00621.hp2 HG02080.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-660G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179694 | ||||||
| chr12:121179864
|
G | A | 1 | a0030c0031t0002g0202 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1189-490G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179864 | ||||||
| chr12:121179868
|
C | T | 3 | a0006c0005t0013g0172a0006c0005t0013g0173a0006c0005t0013g0174 | 3 | HG02257.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1189-486C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179868 | ||||||
| chr12:121179875
|
C | T | 2 | a0003c0004t0001g0114a0003c0004t0001g0138 | 2 | NA18963.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1189-479C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179875 | ||||||
| chr12:121179904
|
C | T | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1189-450C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121179904 | ||||||
| chr12:121180056
|
G | A | 3 | a0011c0011t0005g0177a0019c0022t0005g0244a0019c0022t0005g0308 | 3 | HG02896.hp2 HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1189-298G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121180056 | ||||||
| chr12:121180107
|
C | T | 4 | a0004c0003t0010g0299a0004c0003t0010g0300a0004c0003t0010g0301others(1): Show | 4 | HG01891.hp1 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1189-247C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121180107 | ||||||
| chr12:121180147
|
C | CA | 30 | a0001c0001t0001g0047a0002c0002t0035g0343a0003c0004t0001g0086others(27): Show | 31 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.1189-187dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121180147 | |||||
| chr12:121180147
|
C | CAA | 58 | a0004c0003t0008g0238a0004c0003t0008g0239a0004c0003t0008g0241others(55): Show | 58 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.1189-188_1189-187d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 121180147 | |||||
| chr12:121180187
|
A | G | 6 | a0001c0001t0001g0159a0002c0002t0001g0079a0002c0002t0001g0118others(3): Show | 7 | HG00735.hp1 HG01074.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1189-167A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121180187 | ||||||
| chr12:121180200
|
C | T | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1189-154C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121180200 | ||||||
| chr12:121180338
|
A | C | 14 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(11): Show | 14 | HG01243.hp1 HG01891.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1189-16A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121180338 | ||||||
| chr12:121180340
|
C | T | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1189-14C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 11/12 | chr12 | 121180340 | ||||||
| chr12:121180475
|
CT | C | 46 | a0001c0001t0001g0034a0001c0001t0001g0102a0001c0001t0034g0111others(43): Show | 47 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1290+34delT | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121180475 | |||||
| chr12:121180527
|
C | T | 3 | a0022c0025t0015g0195a0022c0025t0015g0204a0024c0027t0021g0197 | 3 | HG01891.hp2 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1290+72C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180527 | ||||||
| chr12:121180547
|
T | C | 1 | a0004c0003t0004g0232 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1290+92T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180547 | ||||||
| chr12:121180588
|
A | G | 6 | a0004c0003t0011g0133a0010c0010t0011g0278a0010c0010t0011g0279others(3): Show | 6 | HG01074.hp2 HG01168.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+133A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180588 | ||||||
| chr12:121180635
|
C | T | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1290+180C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180635 | ||||||
| chr12:121180761
|
G | A | 13 | a0011c0011t0004g0181a0011c0011t0004g0182a0011c0011t0004g0183others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1290+306G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180761 | ||||||
| chr12:121180765
|
C | G | 7 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(4): Show | 7 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1290+310C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180765 | ||||||
| chr12:121180819
|
C | T | 3 | a0022c0025t0015g0195a0022c0025t0015g0204a0024c0027t0021g0197 | 3 | HG01891.hp2 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1290+364C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180819 | ||||||
| chr12:121180862
|
G | A | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1290+407G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180862 | ||||||
| chr12:121180912
|
C | T | 28 | a0004c0003t0008g0238a0004c0003t0008g0239a0004c0003t0008g0241others(25): Show | 28 | HG01943.hp1 HG02165.hp2 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.1290+457C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180912 | ||||||
| chr12:121180953
|
G | C | 4 | a0017c0020t0002g0322a0017c0020t0002g0335a0017c0020t0002g0345others(1): Show | 4 | HG02965.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290+498G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180953 | ||||||
| chr12:121180959
|
A | G | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1290+504A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121180959 | ||||||
| chr12:121180963
|
C | CA | 32 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(29): Show | 32 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1290+520dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121180963 | |||||
| chr12:121181105
|
G | A | 4 | a0007c0015t0001g0045a0007c0015t0001g0046a0007c0015t0001g0073others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290+650G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181105 | ||||||
| chr12:121181157
|
G | A | 1 | a0014c0014t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1290+702G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181157 | ||||||
| chr12:121181170
|
G | A | 1 | a0006c0005t0002g0143 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1290+715G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181170 | ||||||
| chr12:121181251
|
A | G | 7 | a0002c0002t0003g0298a0002c0002t0003g0302a0002c0002t0003g0317others(4): Show | 7 | HG02132.hp2 NA18941.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1290+796A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181251 | ||||||
| chr12:121181448
|
A | G | 1 | a0008c0007t0002g0324 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1290+993A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181448 | ||||||
| chr12:121181658
|
C | T | 1 | a0002c0002t0033g0294 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1290+1203C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181658 | ||||||
| chr12:121181717
|
C | T | 2 | a0013c0018t0004g0175a0013c0018t0004g0188 | 2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1290+1262C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181717 | ||||||
| chr12:121181718
|
A | G | 109 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1290+1263A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181718 | ||||||
| chr12:121181726
|
G | A | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1290+1271G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121181726 | ||||||
| chr12:121182031
|
T | C | 23 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(20): Show | 23 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1290+1576T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182031 | ||||||
| chr12:121182061
|
T | TA | 57 | a0002c0002t0003g0302a0002c0002t0003g0323a0002c0024t0003g0186others(54): Show | 58 | HG01069.hp2 HG01099.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.1290+1624dupA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121182061 | |||||
| chr12:121182061
|
T | TAA | 25 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(22): Show | 25 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1290+1623_1290+162 others(6): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121182061 | |||||
| chr12:121182061
|
T | TAAAA | 21 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(18): Show | 21 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1290+1621_1290+162 others(8): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121182061 | |||||
| chr12:121182063
|
A | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290+1608A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182063 | ||||||
| chr12:121182171
|
A | C | 112 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(109): Show | 113 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.1290+1716A>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182171 | ||||||
| chr12:121182263
|
C | T | 1 | a0002c0002t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1290+1808C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182263 | ||||||
| chr12:121182342
|
C | T | 32 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(29): Show | 32 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1290+1887C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182342 | ||||||
| chr12:121182384
|
G | T | 55 | a0006c0005t0002g0013a0006c0005t0002g0032a0006c0005t0002g0043others(52): Show | 55 | HG00323.hp1 HG00438.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1291-1921G>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182384 | ||||||
| chr12:121182425
|
T | C | 4 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(1): Show | 4 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1291-1880T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182425 | ||||||
| chr12:121182503
|
C | T | 5 | a0004c0003t0012g0199a0004c0003t0012g0201a0004c0003t0012g0205others(2): Show | 5 | HG00280.hp1 HG00642.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291-1802C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182503 | ||||||
| chr12:121182526
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0096 | 3 | NA18994.hp1 NA19003.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1291-1779G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182526 | ||||||
| chr12:121182584
|
G | A | 3 | a0002c0002t0001g0025a0003c0004t0001g0036a0003c0004t0001g0084 | 3 | HG00558.hp2 NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1291-1721G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182584 | ||||||
| chr12:121182598
|
T | C | 1 | a0002c0002t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291-1707T>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182598 | ||||||
| chr12:121182757
|
C | T | 1 | a0006c0005t0002g0100 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1291-1548C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182757 | ||||||
| chr12:121182963
|
A | G | 108 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(105): Show | 109 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1291-1342A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121182963 | ||||||
| chr12:121183081
|
G | A | 1 | a0003c0004t0001g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1291-1224G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183081 | ||||||
| chr12:121183176
|
CA | C | 106 | a0002c0002t0003g0336a0004c0003t0004g0206a0004c0003t0004g0219others(103): Show | 107 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.1291-1116delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121183176 | |||||
| chr12:121183192
|
C | A | 1 | a0002c0002t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1291-1113C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183192 | ||||||
| chr12:121183442
|
G | A | 108 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(105): Show | 109 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1291-863G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183442 | ||||||
| chr12:121183494
|
C | A | 1 | a0006c0005t0030g0062 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1291-811C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183494 | ||||||
| chr12:121183580
|
A | AAAC | 243 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0011others(240): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1291-719_1291-717d others(5): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121183580 | |||||
| chr12:121183580
|
A | AAC | 109 | a0002c0002t0003g0253a0004c0003t0004g0206a0004c0003t0004g0219others(106): Show | 110 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.1291-724_1291-723i others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121183580 | |||||
| chr12:121183590
|
T | TAC | 5 | a0005c0017t0005g0214a0005c0017t0005g0215a0005c0017t0005g0216others(2): Show | 5 | HG02818.hp2 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1291-693_1291-692d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121183590 | |||||
| chr12:121183590
|
TAC | T | 89 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(86): Show | 89 | HG00099.hp2 HG00621.hp1 HG01069.hp2 others(86): Show |
intron_variant | MODIFIER | c.1291-693_1291-692d others(4): Show |
P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121183590 | |||||
| chr12:121183726
|
C | T | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291-579C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183726 | ||||||
| chr12:121183799
|
A | G | 1 | a0003c0004t0001g0036 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1291-506A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183799 | ||||||
| chr12:121183865
|
C | G | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291-440C>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183865 | ||||||
| chr12:121183866
|
C | A | 9 | a0004c0003t0007g0248a0004c0003t0007g0249a0004c0003t0007g0250others(6): Show | 9 | HG02559.hp2 HG02809.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1291-439C>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183866 | ||||||
| chr12:121183896
|
C | T | 28 | a0004c0003t0008g0238a0004c0003t0008g0239a0004c0003t0008g0241others(25): Show | 28 | HG01943.hp1 HG02165.hp2 HG03017.hp1 others(25): Show |
intron_variant | MODIFIER | c.1291-409C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183896 | ||||||
| chr12:121183934
|
A | G | 108 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(105): Show | 109 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1291-371A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121183934 | ||||||
| chr12:121184014
|
A | G | 106 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(103): Show | 107 | HG00099.hp2 HG00621.hp1 HG01069.hp2 others(104): Show |
intron_variant | MODIFIER | c.1291-291A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121184014 | ||||||
| chr12:121184064
|
CA | C | 114 | a0001c0001t0001g0067a0001c0001t0001g0095a0001c0001t0001g0155others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1291-225delA | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 121184064 | |||||
| chr12:121184174
|
T | G | 2 | a0002c0002t0001g0228a0003c0004t0001g0122 | 2 | HG00558.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1291-131T>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121184174 | ||||||
| chr12:121184204
|
A | G | 23 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(20): Show | 23 | HG00099.hp2 HG00621.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.1291-101A>G | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121184204 | ||||||
| chr12:121184220
|
C | T | 105 | a0004c0003t0004g0206a0004c0003t0004g0219a0004c0003t0004g0220others(102): Show | 106 | HG00099.hp2 HG00280.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1291-85C>T | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121184220 | ||||||
| chr12:121184221
|
G | A | 6 | a0001c0001t0001g0159a0002c0002t0001g0079a0002c0002t0001g0118others(3): Show | 7 | HG00735.hp1 HG01074.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1291-84G>A | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121184221 | ||||||
| chr12:121184263
|
G | C | 1 | a0001c0001t0017g0161 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1291-42G>C | P2RX7 | ENSG00000089041.17 | transcript | ENST00000328963.10 | protein_coding | 12/12 | chr12 | 121184263 |