Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5858 |
|---|---|
| ensemblid | ENSG00000126838.10 |
| hgncid | 9750 |
| symbol | PZP |
| name | PZP alpha-2-macroglobulin like |
| refseq_nuc | NM_002864.3 |
| refseq_prot | NP_002855.2 |
| ensembl_nuc | ENST00000261336.7 |
| ensembl_prot | ENSP00000261336.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 9148840 |
| end | 9208395 |
| strand | - |
| ver | v1.2 |
| region | chr12:9148840-9208395 |
| region5000 | chr12:9143840-9213395 |
| regionname0 | PZP_chr12_9148840_9208395 |
| regionname5000 | PZP_chr12_9143840_9213395 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1482 | 87 | 21 | 17 | 42 | 3 | 4 | 34 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0002 | 0/0 | 1482 | 43 | 6 | 10 | 24 | 2 | 1 | 14 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0003 | 0/0 | 1482 | 27 | 13 | 4 | 8 | 0 | 2 | 8 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0004 | 0/0 | 1482 | 17 | 2 | 10 | 0 | 2 | 3 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0005 | 0/0 | 597 | 17 | 0 | 0 | 15 | 0 | 2 | 11 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0006 | 0/0 | 1482 | 16 | 2 | 1 | 9 | 0 | 4 | 7 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0007 | 0/1 | 1482 | 16 | 3 | 0 | 8 | 2 | 2 | 5 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008 | 0/0 | 1482 | 15 | 6 | 3 | 3 | 0 | 3 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0009 | 0/0 | 1482 | 14 | 0 | 1 | 6 | 3 | 4 | 4 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0010 | 0/0 | 1482 | 11 | 3 | 7 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0011 | 0/0 | 1482 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0012 | 1/0 | 1482 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0013 | 0/0 | 1482 | 6 | 0 | 2 | 1 | 0 | 3 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0014 | 0/0 | 1482 | 5 | 0 | 0 | 2 | 0 | 3 | 2 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0015 | 0/0 | 1482 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0016 | 0/0 | 1482 | 5 | 1 | 2 | 1 | 1 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0017 | 0/0 | 1482 | 5 | 0 | 2 | 1 | 0 | 2 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0018 | 0/0 | 1482 | 4 | 2 | 1 | 1 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0019 | 0/0 | 1482 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0020 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0021 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0022 | 0/0 | 1482 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0023 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0024 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0025 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0026 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0027 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0028 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0029 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0030 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0031 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0032 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0033 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0034 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0035 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0036 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0037 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0038 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4449 | 70 | 7 | 16 | 41 | 2 | 4 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0002 | 0/0 | 4449 | 42 | 6 | 10 | 23 | 2 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0003 | 0/0 | 4449 | 23 | 12 | 2 | 8 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0004 | 0/0 | 4449 | 17 | 2 | 10 | 0 | 2 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0005 | 0/1 | 4449 | 15 | 2 | 0 | 8 | 2 | 2 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0006 | 0/0 | 4449 | 14 | 0 | 1 | 6 | 3 | 4 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0007 | 0/0 | 4449 | 13 | 1 | 1 | 8 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0008 | 0/0 | 4449 | 13 | 0 | 0 | 12 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0009 | 0/0 | 4449 | 10 | 3 | 7 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0010 | 0/0 | 4449 | 7 | 7 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0011 | 0/0 | 4449 | 6 | 0 | 2 | 1 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0012 | 0/0 | 4449 | 5 | 0 | 2 | 0 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0013 | 0/0 | 4449 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0014 | 1/0 | 4449 | 5 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0015 | 0/0 | 4449 | 5 | 0 | 0 | 2 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0016 | 0/0 | 4449 | 5 | 1 | 2 | 1 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0017 | 0/0 | 4449 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0018 | 0/0 | 4449 | 5 | 0 | 2 | 1 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0019 | 0/0 | 4449 | 4 | 0 | 0 | 3 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0020 | 0/0 | 4449 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0021 | 0/0 | 4449 | 3 | 2 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0022 | 0/0 | 4449 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0023 | 0/0 | 4449 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0024 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0025 | 0/0 | 4449 | 2 | 0 | 1 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0026 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0027 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0028 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0029 | 0/0 | 4449 | 2 | 1 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0030 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0031 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0032 | 0/0 | 4449 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0033 | 0/0 | 4449 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0034 | 0/0 | 4449 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0035 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0036 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0037 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0038 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0039 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0040 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0041 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0042 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0043 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0044 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0045 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0046 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0047 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0048 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0049 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0050 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0051 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0052 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0053 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0054 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0055 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0056 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0057 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0058 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0059 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0060 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0061 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0062 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0063 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0064 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0065 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| c0066 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 187 | 334 | 88 | 64 | 132 | 14 | 34 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 2 | 5 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0004 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0006 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0007 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0008 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4449 | 70 | 7 | 16 | 41 | 2 | 4 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0013 | 0/0 | 4449 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0021 | 0/0 | 4449 | 3 | 2 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0026 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0031 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0038 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0046 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0055 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0058 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0059 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0002c0002 | 0/0 | 4449 | 42 | 6 | 10 | 23 | 2 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0002c0065 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0003c0003 | 0/0 | 4449 | 23 | 12 | 2 | 8 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0003c0022 | 0/0 | 4449 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0003c0041 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0004c0004 | 0/0 | 4449 | 17 | 2 | 10 | 0 | 2 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0005c0008 | 0/0 | 4449 | 13 | 0 | 0 | 12 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0005c0019 | 0/0 | 4449 | 4 | 0 | 0 | 3 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0006c0007 | 0/0 | 4449 | 13 | 1 | 1 | 8 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0006c0029 | 0/0 | 4449 | 2 | 1 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0006c0035 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0007c0005 | 0/1 | 4449 | 15 | 2 | 0 | 8 | 2 | 2 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0007c0056 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0012 | 0/0 | 4449 | 5 | 0 | 2 | 0 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0020 | 0/0 | 4449 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0023 | 0/0 | 4449 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0025 | 0/0 | 4449 | 2 | 0 | 1 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0039 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0043 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0057 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0009c0006 | 0/0 | 4449 | 14 | 0 | 1 | 6 | 3 | 4 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0010c0009 | 0/0 | 4449 | 10 | 3 | 7 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0010c0054 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0011c0010 | 0/0 | 4449 | 7 | 7 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0011c0066 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0012c0014 | 1/0 | 4449 | 5 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0012c0024 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0013c0011 | 0/0 | 4449 | 6 | 0 | 2 | 1 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0014c0015 | 0/0 | 4449 | 5 | 0 | 0 | 2 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0015c0017 | 0/0 | 4449 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0016c0016 | 0/0 | 4449 | 5 | 1 | 2 | 1 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0017c0018 | 0/0 | 4449 | 5 | 0 | 2 | 1 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0018c0030 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0018c0037 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0018c0045 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0019c0032 | 0/0 | 4449 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0019c0033 | 0/0 | 4449 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0020c0027 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0021c0028 | 0/0 | 4449 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0022c0034 | 0/0 | 4449 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0023c0050 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0024c0036 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0025c0040 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0026c0051 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0027c0052 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0028c0042 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0029c0053 | 0/0 | 4449 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0030c0044 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0031c0049 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0032c0048 | 0/0 | 4449 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0033c0047 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0034c0060 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0035c0061 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0036c0062 | 0/0 | 4449 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0037c0064 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0038c0063 | 0/0 | 4449 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4635 | 70 | 7 | 16 | 41 | 2 | 4 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0013t0001 | 0/0 | 4635 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0021t0001 | 0/0 | 4635 | 3 | 2 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0026t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0031t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0038t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0046t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0055t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0058t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0001c0059t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0002c0002t0001 | 0/0 | 4635 | 42 | 6 | 10 | 23 | 2 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0002c0065t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0003c0003t0001 | 0/0 | 4635 | 23 | 12 | 2 | 8 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0003c0022t0001 | 0/0 | 4635 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0003c0041t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0004c0004t0001 | 0/0 | 4635 | 17 | 2 | 10 | 0 | 2 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0005c0008t0001 | 0/0 | 4635 | 13 | 0 | 0 | 12 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0005c0019t0001 | 0/0 | 4635 | 4 | 0 | 0 | 3 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0006c0007t0001 | 0/0 | 4635 | 13 | 1 | 1 | 8 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0006c0029t0001 | 0/0 | 4635 | 2 | 1 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0006c0035t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0007c0005t0001 | 0/1 | 4635 | 15 | 2 | 0 | 8 | 2 | 2 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0007c0056t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0012t0001 | 0/0 | 4635 | 5 | 0 | 2 | 0 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0020t0001 | 0/0 | 4635 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0023t0001 | 0/0 | 4635 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0025t0001 | 0/0 | 4635 | 2 | 0 | 1 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0039t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0043t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0008c0057t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0009c0006t0001 | 0/0 | 4635 | 14 | 0 | 1 | 6 | 3 | 4 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0010c0009t0001 | 0/0 | 4635 | 10 | 3 | 7 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0010c0054t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0011c0010t0001 | 0/0 | 4635 | 7 | 7 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0011c0066t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0012c0014t0001 | 1/0 | 4635 | 5 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0012c0024t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0013c0011t0001 | 0/0 | 4635 | 6 | 0 | 2 | 1 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0014c0015t0001 | 0/0 | 4635 | 5 | 0 | 0 | 2 | 0 | 3 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0015c0017t0001 | 0/0 | 4635 | 5 | 5 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0016c0016t0001 | 0/0 | 4635 | 5 | 1 | 2 | 1 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0017c0018t0001 | 0/0 | 4635 | 5 | 0 | 2 | 1 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0018c0030t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0018c0037t0001 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0018c0045t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0019c0032t0001 | 0/0 | 4635 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0019c0033t0001 | 0/0 | 4635 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0020c0027t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0021c0028t0001 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0022c0034t0001 | 0/0 | 4635 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0023c0050t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0024c0036t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0025c0040t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0026c0051t0001 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0027c0052t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0028c0042t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0029c0053t0001 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0030c0044t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0031c0049t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0032c0048t0001 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0033c0047t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0034c0060t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0035c0061t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0036c0062t0001 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0037c0064t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| a0038c0063t0001 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | copy fasta | chr12 | 9143840 | 9213395 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 2 | 5 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0007 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0008 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0013t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0013t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0013t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0013t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0013t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0021t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0021t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0021t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0026t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0026t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0031t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0031t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0038t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0046t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0055t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0058t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0001c0059t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0002c0065t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0022t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0022t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0022t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0003c0041t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0004 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0004c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0008t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0019t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0019t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0019t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0005c0019t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0029t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0029t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0006c0035t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0005t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0007c0056t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0012t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0012t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0012t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0012t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0012t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0020t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0020t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0023t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0025t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0025t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0039t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0043t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0008c0057t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0006 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0009c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0009t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0010c0054t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0011c0010t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0011c0010t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0011c0010t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0011c0010t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0011c0010t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0011c0010t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0011c0066t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0012c0014t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0012c0014t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0012c0014t0001g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0012c0024t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0012c0024t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0013c0011t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0013c0011t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0013c0011t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0013c0011t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0013c0011t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0013c0011t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0014c0015t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0014c0015t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0014c0015t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0014c0015t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0014c0015t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0015c0017t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0015c0017t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0015c0017t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0016c0016t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0016c0016t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0016c0016t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0016c0016t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0016c0016t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0017c0018t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0017c0018t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0017c0018t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0017c0018t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0017c0018t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0018c0030t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0018c0037t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0018c0045t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0019c0032t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0019c0032t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0019c0033t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0019c0033t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0020c0027t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0021c0028t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0021c0028t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0022c0034t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0022c0034t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0023c0050t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0024c0036t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0025c0040t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0026c0051t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0027c0052t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0028c0042t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0029c0053t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0030c0044t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0031c0049t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0032c0048t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0033c0047t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0034c0060t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0035c0061t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0036c0062t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0037c0064t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| a0038c0063t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00099 | hp2 | a0016 | c0016 | t0001 | g0156 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00140 | hp1 | a0004 | c0004 | t0001 | g0275 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00280 | hp1 | a0004 | c0004 | t0001 | g0004 | EUR | FIN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00280 | hp2 | a0029 | c0053 | t0001 | g0195 | EUR | FIN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00408 | hp2 | a0009 | c0006 | t0001 | g0068 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00423 | hp1 | a0005 | c0019 | t0001 | g0180 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00438 | hp2 | a0025 | c0040 | t0001 | g0051 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00609 | hp2 | a0038 | c0063 | t0001 | g0148 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00621 | hp2 | a0037 | c0064 | t0001 | g0171 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00639 | hp2 | a0003 | c0022 | t0001 | g0236 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00642 | hp2 | a0004 | c0004 | t0001 | g0233 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00673 | hp1 | a0002 | c0065 | t0001 | g0138 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | CHS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00735 | hp2 | a0013 | c0011 | t0001 | g0086 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00738 | hp1 | a0018 | c0037 | t0001 | g0257 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG00738 | hp2 | a0017 | c0018 | t0001 | g0166 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01070 | hp1 | a0008 | c0012 | t0001 | g0261 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01070 | hp2 | a0016 | c0016 | t0001 | g0155 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01071 | hp1 | a0008 | c0012 | t0001 | g0263 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01071 | hp2 | a0009 | c0006 | t0001 | g0014 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01074 | hp1 | a0008 | c0025 | t0001 | g0235 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01106 | hp1 | a0004 | c0004 | t0001 | g0224 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01106 | hp2 | a0010 | c0009 | t0001 | g0223 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01109 | hp1 | a0010 | c0009 | t0001 | g0012 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0200 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01168 | hp1 | a0004 | c0004 | t0001 | g0030 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01175 | hp1 | a0026 | c0051 | t0001 | g0207 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01243 | hp1 | a0003 | c0022 | t0001 | g0239 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01257 | hp2 | a0006 | c0007 | t0001 | g0118 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01346 | hp1 | a0004 | c0004 | t0001 | g0260 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01346 | hp2 | a0022 | c0034 | t0001 | g0150 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0199 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01361 | hp1 | a0004 | c0004 | t0001 | g0004 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01361 | hp2 | a0032 | c0048 | t0001 | g0267 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01433 | hp1 | a0010 | c0009 | t0001 | g0244 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01496 | hp1 | a0004 | c0004 | t0001 | g0274 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01516 | hp1 | a0009 | c0006 | t0001 | g0006 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01516 | hp2 | a0007 | c0005 | t0001 | g0018 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01517 | hp1 | a0009 | c0006 | t0001 | g0006 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01517 | hp2 | a0001 | c0058 | t0001 | g0201 | EUR | IBS | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01884 | hp1 | a0011 | c0010 | t0001 | g0109 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01884 | hp2 | a0015 | c0017 | t0001 | g0025 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0203 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01928 | hp1 | a0010 | c0009 | t0001 | g0012 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01928 | hp2 | a0013 | c0011 | t0001 | g0063 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01934 | hp1 | a0016 | c0016 | t0001 | g0140 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01943 | hp2 | a0010 | c0009 | t0001 | g0253 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01952 | hp1 | a0017 | c0018 | t0001 | g0127 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01952 | hp2 | a0010 | c0009 | t0001 | g0229 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01978 | hp1 | a0004 | c0004 | t0001 | g0265 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01978 | hp2 | a0010 | c0009 | t0001 | g0240 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01993 | hp1 | a0001 | c0021 | t0001 | g0123 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG01993 | hp2 | a0004 | c0004 | t0001 | g0234 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02015 | hp2 | a0031 | c0049 | t0001 | g0099 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02040 | hp2 | a0035 | c0061 | t0001 | g0142 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02055 | hp1 | a0001 | c0021 | t0001 | g0193 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02056 | hp1 | a0019 | c0032 | t0001 | g0161 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02071 | hp2 | a0007 | c0005 | t0001 | g0273 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02074 | hp1 | a0005 | c0019 | t0001 | g0174 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02074 | hp2 | a0006 | c0007 | t0001 | g0230 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02080 | hp1 | a0008 | c0023 | t0001 | g0016 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02083 | hp1 | a0007 | c0005 | t0001 | g0033 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02083 | hp2 | a0005 | c0008 | t0001 | g0177 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02129 | hp2 | a0034 | c0060 | t0001 | g0178 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02135 | hp2 | a0009 | c0006 | t0001 | g0070 | EAS | KHV | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02145 | hp1 | a0003 | c0022 | t0001 | g0121 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02145 | hp2 | a0023 | c0050 | t0001 | g0168 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02155 | hp1 | a0007 | c0005 | t0001 | g0044 | EAS | CDX | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02155 | hp2 | a0006 | c0007 | t0001 | g0246 | EAS | CDX | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02257 | hp1 | a0001 | c0013 | t0001 | g0111 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02258 | hp1 | a0001 | c0031 | t0001 | g0212 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02258 | hp2 | a0024 | c0036 | t0001 | g0231 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02273 | hp1 | a0004 | c0004 | t0001 | g0245 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02280 | hp1 | a0001 | c0026 | t0001 | g0034 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02280 | hp2 | a0011 | c0010 | t0001 | g0107 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02293 | hp1 | a0022 | c0034 | t0001 | g0134 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02293 | hp2 | a0004 | c0004 | t0001 | g0225 | AMR | PEL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02451 | hp1 | a0012 | c0014 | t0001 | g0011 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0103 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02572 | hp1 | a0016 | c0016 | t0001 | g0149 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02572 | hp2 | a0001 | c0013 | t0001 | g0277 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02622 | hp1 | a0020 | c0027 | t0001 | g0027 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02622 | hp2 | a0012 | c0014 | t0001 | g0011 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02630 | hp1 | a0010 | c0009 | t0001 | g0037 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02630 | hp2 | a0001 | c0055 | t0001 | g0214 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02647 | hp1 | a0008 | c0020 | t0001 | g0270 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0104 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02683 | hp1 | a0009 | c0006 | t0001 | g0080 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02683 | hp2 | a0017 | c0018 | t0001 | g0169 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02698 | hp1 | a0008 | c0012 | t0001 | g0264 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02698 | hp2 | a0007 | c0005 | t0001 | g0071 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0117 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02717 | hp2 | a0012 | c0024 | t0001 | g0251 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02723 | hp1 | a0020 | c0027 | t0001 | g0027 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02735 | hp1 | a0013 | c0011 | t0001 | g0281 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02735 | hp2 | a0014 | c0015 | t0001 | g0133 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02738 | hp1 | a0006 | c0007 | t0001 | g0232 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02738 | hp2 | a0008 | c0012 | t0001 | g0262 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02809 | hp1 | a0011 | c0066 | t0001 | g0209 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02809 | hp2 | a0018 | c0030 | t0001 | g0024 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02818 | hp1 | a0011 | c0010 | t0001 | g0035 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02818 | hp2 | a0015 | c0017 | t0001 | g0026 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02886 | hp2 | a0011 | c0010 | t0001 | g0108 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02895 | hp2 | a0004 | c0004 | t0001 | g0030 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02922 | hp1 | a0001 | c0059 | t0001 | g0197 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02922 | hp2 | a0036 | c0062 | t0001 | g0218 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0105 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02965 | hp2 | a0006 | c0029 | t0001 | g0098 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02976 | hp2 | a0021 | c0028 | t0001 | g0204 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03017 | hp1 | a0004 | c0004 | t0001 | g0004 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03017 | hp2 | a0017 | c0018 | t0001 | g0170 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0102 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03130 | hp1 | a0018 | c0030 | t0001 | g0024 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03130 | hp2 | a0008 | c0039 | t0001 | g0069 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03139 | hp1 | a0007 | c0056 | t0001 | g0208 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03139 | hp2 | a0006 | c0007 | t0001 | g0256 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03195 | hp1 | a0010 | c0009 | t0001 | g0101 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0228 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03209 | hp2 | a0001 | c0021 | t0001 | g0258 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03225 | hp1 | a0007 | c0005 | t0001 | g0124 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0205 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03239 | hp1 | a0009 | c0006 | t0001 | g0014 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03239 | hp2 | a0006 | c0035 | t0001 | g0041 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03486 | hp1 | a0021 | c0028 | t0001 | g0194 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03486 | hp2 | a0011 | c0010 | t0001 | g0021 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03490 | hp1 | a0004 | c0004 | t0001 | g0029 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03492 | hp1 | a0004 | c0004 | t0001 | g0029 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03492 | hp2 | a0003 | c0041 | t0001 | g0088 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03516 | hp1 | a0011 | c0010 | t0001 | g0110 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03516 | hp2 | a0027 | c0052 | t0001 | g0106 | AFR | ESN | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03540 | hp1 | a0008 | c0020 | t0001 | g0032 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03540 | hp2 | a0015 | c0017 | t0001 | g0219 | AFR | GWD | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03654 | hp1 | a0007 | c0005 | t0001 | g0243 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03654 | hp2 | a0005 | c0008 | t0001 | g0182 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03669 | hp1 | a0014 | c0015 | t0001 | g0128 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03669 | hp2 | a0009 | c0006 | t0001 | g0015 | SAS | PJL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03831 | hp1 | a0010 | c0054 | t0001 | g0221 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03831 | hp2 | a0006 | c0007 | t0001 | g0052 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03834 | hp2 | a0005 | c0019 | t0001 | g0047 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03927 | hp1 | a0013 | c0011 | t0001 | g0280 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0202 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03942 | hp2 | a0008 | c0012 | t0001 | g0259 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG04115 | hp1 | a0006 | c0007 | t0001 | g0252 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG04115 | hp2 | a0009 | c0006 | t0001 | g0220 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0130 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG04184 | hp2 | a0014 | c0015 | t0001 | g0129 | SAS | BEB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG04204 | hp1 | a0013 | c0011 | t0001 | g0055 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18522 | hp1 | a0001 | c0026 | t0001 | g0126 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18522 | hp2 | a0011 | c0010 | t0001 | g0021 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18612 | hp1 | a0008 | c0023 | t0001 | g0016 | EAS | CHB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18612 | hp2 | a0005 | c0008 | t0001 | g0022 | EAS | CHB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0097 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18906 | hp2 | a0008 | c0043 | t0001 | g0272 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18940 | hp2 | a0006 | c0007 | t0001 | g0241 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18947 | hp1 | a0006 | c0007 | t0001 | g0254 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18947 | hp2 | a0017 | c0018 | t0001 | g0120 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18953 | hp2 | a0007 | c0005 | t0001 | g0100 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18959 | hp1 | a0009 | c0006 | t0001 | g0015 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18959 | hp2 | a0007 | c0005 | t0001 | g0033 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18960 | hp1 | a0001 | c0046 | t0001 | g0050 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18961 | hp2 | a0006 | c0007 | t0001 | g0036 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18962 | hp1 | a0005 | c0008 | t0001 | g0022 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18964 | hp1 | a0005 | c0008 | t0001 | g0191 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18967 | hp2 | a0033 | c0047 | t0001 | g0065 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18968 | hp1 | a0007 | c0005 | t0001 | g0271 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18968 | hp2 | a0005 | c0008 | t0001 | g0181 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18969 | hp1 | a0008 | c0025 | t0001 | g0249 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18969 | hp2 | a0016 | c0016 | t0001 | g0153 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18972 | hp1 | a0005 | c0008 | t0001 | g0190 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18974 | hp1 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18974 | hp2 | a0018 | c0045 | t0001 | g0061 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18977 | hp1 | a0006 | c0007 | t0001 | g0222 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18979 | hp1 | a0019 | c0033 | t0001 | g0048 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18982 | hp2 | a0014 | c0015 | t0001 | g0179 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18984 | hp1 | a0009 | c0006 | t0001 | g0079 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0096 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18990 | hp1 | a0005 | c0019 | t0001 | g0175 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18993 | hp2 | a0019 | c0033 | t0001 | g0045 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18995 | hp1 | a0009 | c0006 | t0001 | g0087 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18995 | hp2 | a0019 | c0032 | t0001 | g0167 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18997 | hp1 | a0006 | c0029 | t0001 | g0057 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19000 | hp1 | a0005 | c0008 | t0001 | g0216 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19005 | hp1 | a0006 | c0007 | t0001 | g0248 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0266 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19030 | hp1 | a0030 | c0044 | t0001 | g0255 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0095 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19043 | hp1 | a0001 | c0013 | t0001 | g0279 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19043 | hp2 | a0008 | c0057 | t0001 | g0211 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19056 | hp1 | a0005 | c0008 | t0001 | g0173 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19060 | hp1 | a0007 | c0005 | t0001 | g0237 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19064 | hp1 | a0007 | c0005 | t0001 | g0250 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19064 | hp2 | a0005 | c0008 | t0001 | g0023 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19070 | hp2 | a0006 | c0007 | t0001 | g0247 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19074 | hp2 | a0005 | c0008 | t0001 | g0023 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19077 | hp1 | a0005 | c0008 | t0001 | g0132 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19077 | hp2 | a0009 | c0006 | t0001 | g0084 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19078 | hp1 | a0014 | c0015 | t0001 | g0143 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19078 | hp2 | a0005 | c0008 | t0001 | g0176 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19086 | hp2 | a0013 | c0011 | t0001 | g0238 | EAS | JPT | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19240 | hp1 | a0028 | c0042 | t0001 | g0162 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA19240 | hp2 | a0008 | c0020 | t0001 | g0032 | AFR | YRI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20129 | hp1 | a0001 | c0031 | t0001 | g0213 | AFR | ASW | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20129 | hp2 | a0015 | c0017 | t0001 | g0025 | AFR | ASW | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0185 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20752 | hp2 | a0007 | c0005 | t0001 | g0018 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0187 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20805 | hp2 | a0009 | c0006 | t0001 | g0006 | EUR | TSI | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02109 | hp1 | a0015 | c0017 | t0001 | g0026 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0002 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02486 | hp1 | a0001 | c0013 | t0001 | g0276 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02486 | hp2 | a0007 | c0005 | t0001 | g0122 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG02559 | hp2 | a0012 | c0024 | t0001 | g0242 | AFR | ACB | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03471 | hp1 | a0001 | c0013 | t0001 | g0278 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | MSL | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG06807 | hp1 | a0012 | c0014 | t0001 | g0011 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| HG06807 | hp2 | a0004 | c0004 | t0001 | g0004 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20300 | hp1 | a0001 | c0038 | t0001 | g0119 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA20300 | hp2 | a0010 | c0009 | t0001 | g0012 | AFR | USA | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| NA21309 | hp2 | a0012 | c0014 | t0001 | g0196 | AFR | LWK | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| homoSapiens_chm13v2 | hp1 | a0007 | c0005 | t0001 | g0072 | REF | REF | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| homoSapiens_grch38 | hp1 | a0012 | c0014 | t0001 | g0210 | REF | REF | PZP_chr12_9143840_9213395 | PZP | chr12 | 9143840 | 9213395 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9148976
|
A | G | 1 | a0035 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.4445T>C | p.Val1482Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 36/36 | 4499/4635 | 4445/4449 | 1482/1482 | chr12 | 9148976 | ||
| chr12:9150700
|
A | T | 8 | a0004a0005a0013others(5): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
missense_variant | MODERATE | c.4328T>A | p.Ile1443Asn | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/36 | 4382/4635 | 4328/4449 | 1443/1482 | chr12 | 9150700 | ||
| chr12:9151647
|
C | T | 1 | a0033 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.4238G>A | p.Arg1413Gln | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/36 | 4292/4635 | 4238/4449 | 1413/1482 | chr12 | 9151647 | ||
| chr12:9154620
|
G | A | 1 | a0032 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.3770C>T | p.Thr1257Ile | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/36 | 3824/4635 | 3770/4449 | 1257/1482 | chr12 | 9154620 | ||
| chr12:9154777
|
T | G | 37 | a0001a0002a0003others(34): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
missense_variant | MODERATE | c.3613A>C | p.Thr1205Pro | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/36 | 3667/4635 | 3613/4449 | 1205/1482 | chr12 | 9154777 | ||
| chr12:9157223
|
G | A | 2 | a0020a0030 | 3 | HG02622.hp1 HG02723.hp1 NA19030.hp1 |
stop_gained | HIGH | c.3502C>T | p.Gln1168* | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3556/4635 | 3502/4449 | 1168/1482 | chr12 | 9157223 | ||
| chr12:9157285
|
C | T | 2 | a0020a0030 | 3 | HG02622.hp1 HG02723.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.3440G>A | p.Gly1147Glu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3494/4635 | 3440/4449 | 1147/1482 | chr12 | 9157285 | ||
| chr12:9157287
|
A | T | 1 | a0031 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.3438T>A | p.His1146Gln | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3492/4635 | 3438/4449 | 1146/1482 | chr12 | 9157287 | ||
| chr12:9160355
|
G | A | 13 | a0002a0005a0006others(10): Show | 111 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
missense_variant | MODERATE | c.3008C>T | p.Thr1003Met | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/36 | 3062/4635 | 3008/4449 | 1003/1482 | chr12 | 9160355 | ||
| chr12:9164177
|
T | C | 17 | a0001a0009a0011others(14): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
missense_variant | MODERATE | c.2570A>G | p.Asn857Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 20/36 | 2624/4635 | 2570/4449 | 857/1482 | chr12 | 9164177 | ||
| chr12:9165188
|
A | G | 14 | a0002a0003a0005others(11): Show | 140 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(137): Show |
missense_variant | MODERATE | c.2438T>C | p.Val813Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/36 | 2492/4635 | 2438/4449 | 813/1482 | chr12 | 9165188 | ||
| chr12:9165363
|
A | C | 1 | a0028 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.2263T>G | p.Ser755Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/36 | 2317/4635 | 2263/4449 | 755/1482 | chr12 | 9165363 | ||
| chr12:9168905
|
C | T | 6 | a0003a0019a0021others(3): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
missense_variant | MODERATE | c.2071G>A | p.Val691Met | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/36 | 2125/4635 | 2071/4449 | 691/1482 | chr12 | 9168905 | ||
| chr12:9169485
|
C | T | 1 | a0025 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.1946G>A | p.Gly649Glu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/36 | 2000/4635 | 1946/4449 | 649/1482 | chr12 | 9169485 | ||
| chr12:9169506
|
C | T | 1 | a0024 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1925G>A | p.Arg642His | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/36 | 1979/4635 | 1925/4449 | 642/1482 | chr12 | 9169506 | ||
| chr12:9181030
|
G | A | 1 | a0005 | 17 | HG00423.hp1 HG02074.hp1 HG02083.hp2 others(14): Show |
stop_gained | HIGH | c.1792C>T | p.Gln598* | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/36 | 1846/4635 | 1792/4449 | 598/1482 | chr12 | 9181030 | ||
| chr12:9181062
|
G | A | 1 | a0020 | 2 | HG02622.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.1760C>T | p.Pro587Leu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/36 | 1814/4635 | 1760/4449 | 587/1482 | chr12 | 9181062 | ||
| chr12:9192228
|
G | C | 1 | a0023 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1511C>G | p.Ser504Cys | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/36 | 1565/4635 | 1511/4449 | 504/1482 | chr12 | 9192228 | ||
| chr12:9194196
|
G | C | 13 | a0002a0005a0014others(10): Show | 91 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
missense_variant | MODERATE | c.1135C>G | p.Leu379Val | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/36 | 1189/4635 | 1135/4449 | 379/1482 | chr12 | 9194196 | ||
| chr12:9197118
|
G | A | 1 | a0011 | 8 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(5): Show |
missense_variant | MODERATE | c.761C>T | p.Thr254Ile | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/36 | 815/4635 | 761/4449 | 254/1482 | chr12 | 9197118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9152877
|
T | C | 40 | a0001c0001a0001c0013a0001c0021others(37): Show | 234 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
synonymous_variant | LOW | c.4068A>G | p.Gln1356Gln | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/36 | 4122/4635 | 4068/4449 | 1356/1482 | chr12 | 9152877 | ||
| chr12:9152901
|
A | C | 1 | a0001c0046 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.4044T>G | p.Ala1348Ala | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/36 | 4098/4635 | 4044/4449 | 1348/1482 | chr12 | 9152901 | ||
| chr12:9157350
|
A | G | 1 | a0008c0039 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.3375T>C | p.Pro1125Pro | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/36 | 3429/4635 | 3375/4449 | 1125/1482 | chr12 | 9157350 | ||
| chr12:9158429
|
A | G | 4 | a0008c0020a0008c0043a0018c0030others(1): Show | 7 | HG02258.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
synonymous_variant | LOW | c.3285T>C | p.Asn1095Asn | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/36 | 3339/4635 | 3285/4449 | 1095/1482 | chr12 | 9158429 | ||
| chr12:9162613
|
A | G | 30 | a0001c0001a0001c0013a0001c0021others(27): Show | 138 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(135): Show |
synonymous_variant | LOW | c.2772T>C | p.Ser924Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/36 | 2826/4635 | 2772/4449 | 924/1482 | chr12 | 9162613 | ||
| chr12:9165289
|
G | A | 16 | a0001c0001a0001c0046a0001c0058others(13): Show | 107 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
synonymous_variant | LOW | c.2337C>T | p.Ser779Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/36 | 2391/4635 | 2337/4449 | 779/1482 | chr12 | 9165289 | ||
| chr12:9168879
|
T | C | 7 | a0001c0013a0001c0021a0001c0038others(4): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
synonymous_variant | LOW | c.2097A>G | p.Gly699Gly | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/36 | 2151/4635 | 2097/4449 | 699/1482 | chr12 | 9168879 | ||
| chr12:9168924
|
C | T | 1 | a0024c0036 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.2052G>A | p.Ser684Ser | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/36 | 2106/4635 | 2052/4449 | 684/1482 | chr12 | 9168924 | ||
| chr12:9181019
|
C | A | 1 | a0002c0065 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1803G>T | p.Leu601Leu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/36 | 1857/4635 | 1803/4449 | 601/1482 | chr12 | 9181019 | ||
| chr12:9181975
|
C | T | 11 | a0001c0055a0003c0003a0003c0022others(8): Show | 37 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(34): Show |
splice_region_variant&synonymous_variant | LOW | c.1689G>A | p.Lys563Lys | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/36 | 1743/4635 | 1689/4449 | 563/1482 | chr12 | 9181975 | ||
| chr12:9181999
|
C | T | 4 | a0001c0021a0001c0038a0011c0010others(1): Show | 12 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(9): Show |
synonymous_variant | LOW | c.1665G>A | p.Glu555Glu | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/36 | 1719/4635 | 1665/4449 | 555/1482 | chr12 | 9181999 | ||
| chr12:9192677
|
A | G | 49 | a0001c0001a0001c0013a0001c0021others(46): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
synonymous_variant | LOW | c.1317T>C | p.Gly439Gly | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 12/36 | 1371/4635 | 1317/4449 | 439/1482 | chr12 | 9192677 | ||
| chr12:9197114
|
A | G | 2 | a0008c0020a0024c0036 | 4 | HG02258.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
synonymous_variant | LOW | c.765T>C | p.Tyr255Tyr | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/36 | 819/4635 | 765/4449 | 255/1482 | chr12 | 9197114 | ||
| chr12:9202610
|
C | T | 1 | a0006c0035 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.342G>A | p.Arg114Arg | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 3/36 | 396/4635 | 342/4449 | 114/1482 | chr12 | 9202610 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:9149459
|
G | A | 1 | a0004c0004t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4426+102C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 35/35 | chr12 | 9149459 | ||||||
| chr12:9149717
|
A | G | 32 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(29): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.4385-115T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9149717 | ||||||
| chr12:9149860
|
A | G | 1 | a0012c0024t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4385-258T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9149860 | ||||||
| chr12:9150107
|
T | G | 1 | a0008c0039t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4385-505A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150107 | ||||||
| chr12:9150118
|
T | A | 1 | a0010c0009t0001g0240 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4385-516A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150118 | ||||||
| chr12:9150119
|
A | C | 1 | a0011c0066t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4385-517T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150119 | ||||||
| chr12:9150285
|
G | C | 1 | a0007c0005t0001g0072 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4384+359C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150285 | ||||||
| chr12:9150294
|
T | G | 1 | a0001c0001t0001g0067 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.4384+350A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150294 | ||||||
| chr12:9150310
|
T | G | 1 | a0008c0039t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4384+334A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150310 | ||||||
| chr12:9150314
|
G | T | 8 | a0001c0026t0001g0034a0001c0026t0001g0126a0001c0031t0001g0212others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4384+330C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150314 | ||||||
| chr12:9150329
|
C | T | 2 | a0020c0027t0001g0027a0030c0044t0001g0255 | 3 | HG02622.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4384+315G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150329 | ||||||
| chr12:9150344
|
G | A | 32 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(29): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.4384+300C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150344 | ||||||
| chr12:9150385
|
C | T | 1 | a0016c0016t0001g0153 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.4384+259G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 34/35 | chr12 | 9150385 | ||||||
| chr12:9150753
|
G | C | 40 | a0001c0038t0001g0119a0003c0003t0001g0002a0003c0003t0001g0019others(37): Show | 45 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(42): Show |
splice_region_variant&intron_variant | LOW | c.4282-7C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150753 | ||||||
| chr12:9150759
|
G | C | 1 | a0005c0008t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4282-13C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150759 | ||||||
| chr12:9150844
|
A | G | 92 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(89): Show | 107 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.4282-98T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150844 | ||||||
| chr12:9150917
|
C | A | 1 | a0001c0021t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4282-171G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9150917 | ||||||
| chr12:9151337
|
G | T | 1 | a0008c0020t0001g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4281+267C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151337 | ||||||
| chr12:9151432
|
A | G | 8 | a0001c0026t0001g0034a0001c0026t0001g0126a0001c0031t0001g0212others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.4281+172T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151432 | ||||||
| chr12:9151504
|
C | A | 1 | a0001c0001t0001g0060 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4281+100G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151504 | ||||||
| chr12:9151524
|
G | A | 1 | a0011c0066t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4281+80C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151524 | ||||||
| chr12:9151549
|
C | G | 1 | a0021c0028t0001g0204 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4281+55G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 33/35 | chr12 | 9151549 | ||||||
| chr12:9152375
|
C | T | 1 | a0002c0002t0001g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4122-65G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152375 | ||||||
| chr12:9152412
|
G | A | 1 | a0017c0018t0001g0170 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4122-102C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152412 | ||||||
| chr12:9152444
|
T | A | 2 | a0001c0021t0001g0258a0018c0037t0001g0257 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4122-134A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152444 | ||||||
| chr12:9152701
|
T | C | 1 | a0010c0009t0001g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4121+123A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 31/35 | chr12 | 9152701 | ||||||
| chr12:9153096
|
C | T | 1 | a0032c0048t0001g0267 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3993+29G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 30/35 | chr12 | 9153096 | ||||||
| chr12:9153354
|
C | T | 1 | a0001c0058t0001g0201 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3775-11G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153354 | ||||||
| chr12:9153390
|
A | G | 5 | a0008c0020t0001g0032a0008c0020t0001g0270a0008c0043t0001g0272others(2): Show | 7 | HG02258.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3775-47T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153390 | ||||||
| chr12:9153639
|
A | T | 1 | a0034c0060t0001g0178 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3775-296T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153639 | ||||||
| chr12:9153984
|
G | A | 1 | a0007c0005t0001g0273 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3774+632C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9153984 | ||||||
| chr12:9154180
|
G | A | 1 | a0005c0008t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3774+436C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9154180 | ||||||
| chr12:9154222
|
T | C | 1 | a0003c0041t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3774+394A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9154222 | ||||||
| chr12:9154399
|
C | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(196): Show | 238 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.3774+217G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 29/35 | chr12 | 9154399 | ||||||
| chr12:9155042
|
G | A | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3551-203C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155042 | ||||||
| chr12:9155156
|
C | T | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3551-317G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155156 | ||||||
| chr12:9155166
|
C | T | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3551-327G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155166 | ||||||
| chr12:9155326
|
G | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(273): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3551-487C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155326 | ||||||
| chr12:9155345
|
C | G | 1 | a0002c0002t0001g0147 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3551-506G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155345 | ||||||
| chr12:9155492
|
A | G | 1 | a0008c0025t0001g0235 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3551-653T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155492 | ||||||
| chr12:9155492
|
ATTG | A | 93 | a0001c0001t0001g0092a0002c0002t0001g0003a0002c0002t0001g0010others(90): Show | 108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.3551-656_3551-654d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155492 | ||||||
| chr12:9155623
|
A | G | 2 | a0001c0021t0001g0123a0001c0021t0001g0193 | 2 | HG01993.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3551-784T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155623 | ||||||
| chr12:9155916
|
A | G | 1 | a0008c0039t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3551-1077T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155916 | ||||||
| chr12:9155929
|
A | G | 41 | a0001c0038t0001g0119a0003c0003t0001g0002a0003c0003t0001g0019others(38): Show | 47 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.3551-1090T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155929 | ||||||
| chr12:9155955
|
G | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(228): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.3551-1116C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9155955 | ||||||
| chr12:9156233
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3550+942T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156233 | ||||||
| chr12:9156266
|
G | A | 1 | a0001c0001t0001g0008 | 3 | HG02976.hp1 HG03453.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.3550+909C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156266 | ||||||
| chr12:9156928
|
T | A | 1 | a0017c0018t0001g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3550+247A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156928 | ||||||
| chr12:9156935
|
G | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(273): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3550+240C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156935 | ||||||
| chr12:9156970
|
G | A | 8 | a0001c0026t0001g0034a0001c0026t0001g0126a0001c0031t0001g0212others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3550+205C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9156970 | ||||||
| chr12:9157085
|
G | C | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3550+90C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 28/35 | chr12 | 9157085 | ||||||
| chr12:9157399
|
G | A | 32 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(29): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3370-44C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 27/35 | chr12 | 9157399 | ||||||
| chr12:9157412
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(276): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.3370-57A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 27/35 | chr12 | 9157412 | ||||||
| chr12:9157555
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(195): Show | 237 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.3370-200G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 27/35 | chr12 | 9157555 | ||||||
| chr12:9157929
|
C | A | 2 | a0001c0055t0001g0214a0027c0052t0001g0106 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3295-88G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157929 | ||||||
| chr12:9157969
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(195): Show | 237 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.3295-128G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157969 | ||||||
| chr12:9157979
|
GT | G | 93 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(90): Show | 108 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.3295-139delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157979 | ||||||
| chr12:9157980
|
T | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.3295-139A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9157980 | ||||||
| chr12:9158076
|
A | C | 1 | a0002c0002t0001g0188 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3295-235T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9158076 | ||||||
| chr12:9158363
|
C | T | 230 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(227): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.3294+57G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 26/35 | chr12 | 9158363 | ||||||
| chr12:9158581
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | splice_region_variant&intron_variant | LOW | c.3138-5C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158581 | ||||||
| chr12:9158655
|
C | G | 32 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(29): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-79G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158655 | ||||||
| chr12:9158669
|
A | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(228): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.3138-93T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158669 | ||||||
| chr12:9158685
|
C | T | 32 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(29): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-109G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158685 | ||||||
| chr12:9158752
|
C | CT | 30 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(27): Show | 35 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.3138-177dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158752 | ||||||
| chr12:9158757
|
C | T | 32 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(29): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-181G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | ||||||
| chr12:9158757
|
CT | C | 36 | a0001c0038t0001g0119a0003c0003t0001g0002a0003c0003t0001g0019others(33): Show | 41 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.3138-182delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | ||||||
| chr12:9158757
|
CTT | C | 8 | a0001c0026t0001g0034a0008c0020t0001g0032a0008c0020t0001g0270others(5): Show | 10 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.3138-183_3138-182d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | ||||||
| chr12:9158757
|
CTTT | C | 102 | a0001c0001t0001g0075a0001c0001t0001g0183a0001c0026t0001g0126others(99): Show | 118 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.3138-184_3138-182d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | ||||||
| chr12:9158757
|
CTTTT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(89): Show | 115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.3138-185_3138-182d others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9158757 | ||||||
| chr12:9159077
|
A | C | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3138-501T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159077 | ||||||
| chr12:9159082
|
G | A | 32 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(29): Show | 37 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.3138-506C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159082 | ||||||
| chr12:9159134
|
G | T | 5 | a0010c0009t0001g0037a0010c0009t0001g0101a0015c0017t0001g0025others(2): Show | 7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3138-558C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159134 | ||||||
| chr12:9159372
|
C | A | 1 | a0001c0021t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3137+566G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159372 | ||||||
| chr12:9159428
|
T | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(232): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.3137+510A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159428 | ||||||
| chr12:9159505
|
T | C | 2 | a0013c0011t0001g0280a0013c0011t0001g0281 | 2 | HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3137+433A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159505 | ||||||
| chr12:9159885
|
A | G | 1 | a0001c0001t0001g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3137+53T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 25/35 | chr12 | 9159885 | ||||||
| chr12:9160141
|
A | G | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3050-116T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160141 | ||||||
| chr12:9160150
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3050-125A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160150 | ||||||
| chr12:9160183
|
A | G | 1 | a0008c0039t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3049+131T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160183 | ||||||
| chr12:9160276
|
T | C | 3 | a0014c0015t0001g0128a0014c0015t0001g0129a0014c0015t0001g0133 | 3 | HG02735.hp2 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.3049+38A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 24/35 | chr12 | 9160276 | ||||||
| chr12:9160573
|
CAG | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(194): Show | 236 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.2873-85_2873-84del others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160573 | ||||||
| chr12:9160708
|
A | G | 33 | a0002c0065t0001g0138a0004c0004t0001g0004a0004c0004t0001g0029others(30): Show | 38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.2873-218T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160708 | ||||||
| chr12:9160781
|
G | A | 92 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(89): Show | 107 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.2872+252C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160781 | ||||||
| chr12:9160783
|
C | T | 1 | a0001c0001t0001g0007 | 3 | HG00140.hp2 HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2872+250G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160783 | ||||||
| chr12:9160788
|
G | A | 1 | a0004c0004t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2872+245C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160788 | ||||||
| chr12:9160840
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(273): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2872+193T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160840 | ||||||
| chr12:9160887
|
C | G | 4 | a0002c0002t0001g0136a0002c0002t0001g0145a0002c0002t0001g0146others(1): Show | 4 | NA18967.hp1 NA18975.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2872+146G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160887 | ||||||
| chr12:9160922
|
T | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(226): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2872+111A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160922 | ||||||
| chr12:9160924
|
A | G | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2872+109T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9160924 | ||||||
| chr12:9161020
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2872+13C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 23/35 | chr12 | 9161020 | ||||||
| chr12:9161212
|
C | T | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2789-96G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161212 | ||||||
| chr12:9161277
|
A | G | 1 | a0007c0005t0001g0273 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2789-161T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161277 | ||||||
| chr12:9161363
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2789-247C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161363 | ||||||
| chr12:9161471
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2789-355C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161471 | ||||||
| chr12:9161611
|
A | G | 81 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0043others(78): Show | 94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2789-495T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161611 | ||||||
| chr12:9161862
|
G | A | 1 | a0002c0002t0001g0157 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2788+735C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9161862 | ||||||
| chr12:9162013
|
G | A | 5 | a0001c0026t0001g0034a0001c0026t0001g0126a0001c0031t0001g0212others(2): Show | 5 | HG02258.hp1 HG02280.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2788+584C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162013 | ||||||
| chr12:9162032
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2788+565C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162032 | ||||||
| chr12:9162074
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2788+523C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162074 | ||||||
| chr12:9162106
|
C | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(103): Show | 132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2788+491G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162106 | ||||||
| chr12:9162209
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2788+388C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162209 | ||||||
| chr12:9162261
|
T | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(149): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.2788+336A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162261 | ||||||
| chr12:9162392
|
G | A | 3 | a0001c0001t0001g0192a0013c0011t0001g0280a0013c0011t0001g0281 | 3 | HG02735.hp1 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2788+205C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 22/35 | chr12 | 9162392 | ||||||
| chr12:9162909
|
C | A | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.2737-261G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9162909 | ||||||
| chr12:9162948
|
C | T | 1 | a0005c0008t0001g0023 | 2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2737-300G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9162948 | ||||||
| chr12:9163009
|
T | C | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2737-361A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163009 | ||||||
| chr12:9163072
|
G | T | 90 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(87): Show | 100 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2737-424C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163072 | ||||||
| chr12:9163162
|
G | A | 3 | a0014c0015t0001g0128a0014c0015t0001g0129a0014c0015t0001g0133 | 3 | HG02735.hp2 HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2736+506C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163162 | ||||||
| chr12:9163280
|
G | A | 1 | a0016c0016t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2736+388C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163280 | ||||||
| chr12:9163296
|
CA | C | 91 | a0001c0013t0001g0277a0001c0026t0001g0034a0001c0026t0001g0126others(88): Show | 102 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.2736+371delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163296 | ||||||
| chr12:9163296
|
CAA | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 162 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.2736+370_2736+371d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163296 | ||||||
| chr12:9163296
|
CAAAA | C | 44 | a0004c0004t0001g0004a0004c0004t0001g0029a0004c0004t0001g0030others(41): Show | 54 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.2736+368_2736+371d others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163296 | ||||||
| chr12:9163411
|
A | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(273): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2736+257T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163411 | ||||||
| chr12:9163452
|
CA | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(100): Show | 129 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.2736+215delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163452 | ||||||
| chr12:9163531
|
GC | G | 8 | a0003c0003t0001g0019a0003c0003t0001g0042a0003c0003t0001g0054others(5): Show | 9 | NA18953.hp1 NA18970.hp2 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.2736+136delG | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 21/35 | chr12 | 9163531 | ||||||
| chr12:9163882
|
G | T | 2 | a0008c0012t0001g0259a0008c0012t0001g0262 | 2 | HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2615-93C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 20/35 | chr12 | 9163882 | ||||||
| chr12:9164311
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(106): Show | 136 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2488-52G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9164311 | ||||||
| chr12:9164563
|
A | T | 1 | a0013c0011t0001g0055 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2488-304T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9164563 | ||||||
| chr12:9164807
|
G | T | 106 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(103): Show | 131 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2487+332C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9164807 | ||||||
| chr12:9165050
|
C | T | 1 | a0012c0024t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2487+89G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 19/35 | chr12 | 9165050 | ||||||
| chr12:9165405
|
T | C | 2 | a0001c0001t0001g0064a0009c0006t0001g0079 | 2 | NA18984.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.2259-38A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165405 | ||||||
| chr12:9165573
|
ACAAATGA others(8): Show |
A | 1 | a0009c0006t0001g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2259-221_2259-207d others(17): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165573 | ||||||
| chr12:9165683
|
T | A | 1 | a0001c0001t0001g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2259-316A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165683 | ||||||
| chr12:9165692
|
A | T | 1 | a0001c0001t0001g0125 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2259-325T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165692 | ||||||
| chr12:9165900
|
T | C | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2258+152A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 18/35 | chr12 | 9165900 | ||||||
| chr12:9166613
|
G | A | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.2108-411C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166613 | ||||||
| chr12:9166629
|
T | C | 2 | a0001c0021t0001g0258a0018c0037t0001g0257 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2108-427A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166629 | ||||||
| chr12:9166672
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(220): Show | 262 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2108-470G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166672 | ||||||
| chr12:9166772
|
G | A | 1 | a0015c0017t0001g0219 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2108-570C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166772 | ||||||
| chr12:9166820
|
A | G | 1 | a0003c0041t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2108-618T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166820 | ||||||
| chr12:9166881
|
G | A | 1 | a0004c0004t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2108-679C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166881 | ||||||
| chr12:9166924
|
T | G | 1 | a0008c0039t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2108-722A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166924 | ||||||
| chr12:9166934
|
T | C | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2108-732A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9166934 | ||||||
| chr12:9167119
|
G | A | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.2108-917C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167119 | ||||||
| chr12:9167238
|
C | T | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2108-1036G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167238 | ||||||
| chr12:9167273
|
G | A | 1 | a0019c0033t0001g0048 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2108-1071C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167273 | ||||||
| chr12:9167534
|
G | T | 47 | a0002c0002t0001g0172a0002c0002t0001g0184a0002c0002t0001g0185others(44): Show | 52 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.2108-1332C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167534 | ||||||
| chr12:9167615
|
T | C | 1 | a0016c0016t0001g0153 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2107+1254A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167615 | ||||||
| chr12:9167665
|
T | C | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2107+1204A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9167665 | ||||||
| chr12:9168065
|
C | T | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2107+804G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168065 | ||||||
| chr12:9168242
|
A | G | 1 | a0027c0052t0001g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2107+627T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168242 | ||||||
| chr12:9168265
|
C | T | 6 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+604G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168265 | ||||||
| chr12:9168303
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(189): Show | 228 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.2107+566C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168303 | ||||||
| chr12:9168364
|
G | A | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.2107+505C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168364 | ||||||
| chr12:9168493
|
T | C | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2107+376A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168493 | ||||||
| chr12:9168529
|
T | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2107+340A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168529 | ||||||
| chr12:9168671
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2107+198G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168671 | ||||||
| chr12:9168689
|
A | T | 1 | a0005c0008t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2107+180T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 17/35 | chr12 | 9168689 | ||||||
| chr12:9169081
|
C | T | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.2002-107G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169081 | ||||||
| chr12:9169176
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2002-202C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169176 | ||||||
| chr12:9169177
|
C | CA | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2002-204dupT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169177 | ||||||
| chr12:9169180
|
AT | A | 173 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(170): Show | 208 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2002-207delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169180 | ||||||
| chr12:9169181
|
T | A | 54 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(51): Show | 59 | HG00639.hp2 HG00738.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.2002-207A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169181 | ||||||
| chr12:9169300
|
G | A | 1 | a0003c0022t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2001+130C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169300 | ||||||
| chr12:9169311
|
G | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(225): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.2001+119C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 16/35 | chr12 | 9169311 | ||||||
| chr12:9169697
|
G | T | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1840-106C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169697 | ||||||
| chr12:9169702
|
T | C | 6 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840-111A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169702 | ||||||
| chr12:9169798
|
A | T | 5 | a0010c0009t0001g0037a0015c0017t0001g0025a0015c0017t0001g0026others(2): Show | 7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1840-207T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169798 | ||||||
| chr12:9169816
|
A | C | 1 | a0012c0024t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1840-225T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169816 | ||||||
| chr12:9169885
|
A | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1840-294T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169885 | ||||||
| chr12:9169889
|
G | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(203): Show | 245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1840-298C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169889 | ||||||
| chr12:9169923
|
C | A | 1 | a0001c0001t0001g0040 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1840-332G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9169923 | ||||||
| chr12:9170062
|
A | G | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-471T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170062 | ||||||
| chr12:9170235
|
G | A | 2 | a0008c0020t0001g0032a0008c0020t0001g0270 | 3 | HG02647.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1840-644C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170235 | ||||||
| chr12:9170367
|
T | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(79): Show | 106 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.1840-776A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170367 | ||||||
| chr12:9170405
|
C | T | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1840-814G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170405 | ||||||
| chr12:9170431
|
G | C | 2 | a0003c0003t0001g0160a0003c0003t0001g0266 | 2 | NA18999.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1840-840C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170431 | ||||||
| chr12:9170475
|
G | A | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-884C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170475 | ||||||
| chr12:9170703
|
C | T | 2 | a0003c0022t0001g0236a0003c0022t0001g0239 | 2 | HG00639.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1840-1112G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170703 | ||||||
| chr12:9170857
|
C | T | 44 | a0002c0002t0001g0172a0002c0002t0001g0184a0002c0002t0001g0187others(41): Show | 49 | HG00280.hp2 HG00423.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1840-1266G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170857 | ||||||
| chr12:9170881
|
C | T | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-1290G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170881 | ||||||
| chr12:9170944
|
G | A | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-1353C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9170944 | ||||||
| chr12:9171100
|
C | T | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1840-1509G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171100 | ||||||
| chr12:9171109
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(221): Show | 264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1840-1518T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171109 | ||||||
| chr12:9171201
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1840-1610G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171201 | ||||||
| chr12:9171216
|
C | T | 1 | a0002c0002t0001g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1840-1625G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171216 | ||||||
| chr12:9171358
|
A | C | 1 | a0004c0004t0001g0029 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1840-1767T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171358 | ||||||
| chr12:9171387
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(225): Show | 269 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.1840-1796A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171387 | ||||||
| chr12:9171411
|
T | G | 3 | a0008c0020t0001g0032a0008c0020t0001g0270a0024c0036t0001g0231 | 4 | HG02258.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1840-1820A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171411 | ||||||
| chr12:9171423
|
G | A | 6 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840-1832C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171423 | ||||||
| chr12:9171535
|
G | A | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-1944C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171535 | ||||||
| chr12:9171543
|
C | T | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-1952G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171543 | ||||||
| chr12:9171652
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1840-2061G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171652 | ||||||
| chr12:9171774
|
G | C | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1840-2183C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9171774 | ||||||
| chr12:9172017
|
A | G | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-2426T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172017 | ||||||
| chr12:9172081
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1840-2490T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172081 | ||||||
| chr12:9172094
|
A | C | 2 | a0001c0001t0001g0125a0017c0018t0001g0127 | 2 | HG01891.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1840-2503T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172094 | ||||||
| chr12:9172245
|
C | T | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-2654G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172245 | ||||||
| chr12:9172477
|
A | G | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-2886T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172477 | ||||||
| chr12:9172585
|
G | A | 1 | a0029c0053t0001g0195 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1840-2994C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172585 | ||||||
| chr12:9172600
|
C | T | 20 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(17): Show | 23 | HG00738.hp1 HG00738.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.1840-3009G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172600 | ||||||
| chr12:9172776
|
ACTAT | A | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1840-3189_1840-318 others(8): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172776 | ||||||
| chr12:9172875
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1840-3284C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172875 | ||||||
| chr12:9172933
|
A | G | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1840-3342T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9172933 | ||||||
| chr12:9173011
|
C | T | 1 | a0005c0008t0001g0023 | 2 | NA19064.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1840-3420G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173011 | ||||||
| chr12:9173189
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1840-3598T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173189 | ||||||
| chr12:9173266
|
T | C | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1840-3675A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173266 | ||||||
| chr12:9173297
|
T | C | 1 | a0004c0004t0001g0234 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1840-3706A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173297 | ||||||
| chr12:9173416
|
G | A | 1 | a0004c0004t0001g0030 | 2 | HG01168.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1840-3825C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173416 | ||||||
| chr12:9173450
|
A | G | 6 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(3): Show | 6 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1840-3859T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173450 | ||||||
| chr12:9173463
|
T | C | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-3872A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173463 | ||||||
| chr12:9173509
|
C | G | 4 | a0007c0005t0001g0122a0007c0005t0001g0124a0007c0056t0001g0208others(1): Show | 5 | HG02486.hp2 HG02809.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1840-3918G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173509 | ||||||
| chr12:9173555
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1840-3964T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173555 | ||||||
| chr12:9173598
|
A | G | 1 | a0006c0007t0001g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1840-4007T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173598 | ||||||
| chr12:9173615
|
A | G | 1 | a0006c0029t0001g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1840-4024T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173615 | ||||||
| chr12:9173646
|
A | T | 91 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(88): Show | 102 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1840-4055T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173646 | ||||||
| chr12:9173776
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1840-4185T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9173776 | ||||||
| chr12:9174083
|
A | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1840-4492T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174083 | ||||||
| chr12:9174192
|
C | T | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1840-4601G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174192 | ||||||
| chr12:9174203
|
A | G | 1 | a0008c0057t0001g0211 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1840-4612T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174203 | ||||||
| chr12:9174564
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(78): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1840-4973T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174564 | ||||||
| chr12:9174575
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1840-4984G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174575 | ||||||
| chr12:9174614
|
C | A | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1840-5023G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174614 | ||||||
| chr12:9174662
|
C | A | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-5071G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174662 | ||||||
| chr12:9174845
|
A | G | 10 | a0004c0004t0001g0225a0004c0004t0001g0233a0004c0004t0001g0260others(7): Show | 10 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1840-5254T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174845 | ||||||
| chr12:9174879
|
A | G | 1 | a0005c0008t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1840-5288T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174879 | ||||||
| chr12:9174906
|
A | G | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1840-5315T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174906 | ||||||
| chr12:9174955
|
A | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1840-5364T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9174955 | ||||||
| chr12:9175035
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1840-5444C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175035 | ||||||
| chr12:9175067
|
C | A | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1840-5476G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175067 | ||||||
| chr12:9175193
|
A | G | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1840-5602T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175193 | ||||||
| chr12:9175661
|
A | C | 1 | a0007c0005t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1839+5322T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175661 | ||||||
| chr12:9175684
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1839+5299G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175684 | ||||||
| chr12:9175825
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1839+5158C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175825 | ||||||
| chr12:9175841
|
GC | G | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+5141delG | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175841 | ||||||
| chr12:9175876
|
C | T | 2 | a0001c0021t0001g0258a0018c0037t0001g0257 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1839+5107G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9175876 | ||||||
| chr12:9176033
|
C | T | 1 | a0009c0006t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1839+4950G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176033 | ||||||
| chr12:9176132
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1839+4851T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176132 | ||||||
| chr12:9176149
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1839+4834G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176149 | ||||||
| chr12:9176411
|
A | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0125a0017c0018t0001g0127 | 3 | HG01891.hp2 HG01952.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1839+4572T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176411 | ||||||
| chr12:9176476
|
T | G | 8 | a0001c0038t0001g0119a0001c0055t0001g0214a0011c0010t0001g0021others(5): Show | 9 | HG01884.hp1 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+4507A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176476 | ||||||
| chr12:9176554
|
T | C | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+4429A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176554 | ||||||
| chr12:9176624
|
C | T | 1 | a0011c0066t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1839+4359G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176624 | ||||||
| chr12:9176952
|
G | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1839+4031C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9176952 | ||||||
| chr12:9177003
|
T | G | 18 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(15): Show | 19 | HG00738.hp1 HG01884.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.1839+3980A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177003 | ||||||
| chr12:9177134
|
T | C | 1 | a0005c0008t0001g0177 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1839+3849A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177134 | ||||||
| chr12:9177196
|
A | G | 17 | a0002c0002t0001g0172a0002c0002t0001g0189a0005c0008t0001g0022others(14): Show | 19 | HG00423.hp1 HG00673.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1839+3787T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177196 | ||||||
| chr12:9177278
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1839+3705A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177278 | ||||||
| chr12:9177353
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(203): Show | 245 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1839+3630A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177353 | ||||||
| chr12:9177552
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1839+3431C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177552 | ||||||
| chr12:9177821
|
A | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(221): Show | 264 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1839+3162T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177821 | ||||||
| chr12:9177933
|
A | G | 1 | a0007c0005t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1839+3050T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9177933 | ||||||
| chr12:9178009
|
T | C | 91 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(88): Show | 102 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1839+2974A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178009 | ||||||
| chr12:9178469
|
A | G | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+2514T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178469 | ||||||
| chr12:9178576
|
G | A | 1 | a0001c0013t0001g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1839+2407C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178576 | ||||||
| chr12:9178813
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1839+2170C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178813 | ||||||
| chr12:9178905
|
TCA | T | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+2076_1839+207 others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9178905 | ||||||
| chr12:9179288
|
T | G | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1839+1695A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179288 | ||||||
| chr12:9179486
|
A | G | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1839+1497T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179486 | ||||||
| chr12:9179593
|
A | G | 4 | a0001c0026t0001g0034a0001c0026t0001g0126a0011c0066t0001g0209others(1): Show | 4 | HG02280.hp1 HG02809.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839+1390T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179593 | ||||||
| chr12:9179750
|
C | T | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1839+1233G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179750 | ||||||
| chr12:9179983
|
C | T | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1839+1000G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9179983 | ||||||
| chr12:9180011
|
C | T | 32 | a0003c0003t0001g0002a0003c0003t0001g0019a0003c0003t0001g0042others(29): Show | 36 | HG00639.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+972G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180011 | ||||||
| chr12:9180205
|
A | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0125a0017c0018t0001g0127 | 3 | HG01891.hp2 HG01952.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1839+778T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180205 | ||||||
| chr12:9180224
|
G | A | 29 | a0001c0001t0001g0028a0004c0004t0001g0004a0004c0004t0001g0029others(26): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.1839+759C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180224 | ||||||
| chr12:9180233
|
T | C | 3 | a0004c0004t0001g0225a0004c0004t0001g0260a0004c0004t0001g0265 | 3 | HG01346.hp1 HG01978.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1839+750A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180233 | ||||||
| chr12:9180329
|
C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1839+654G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180329 | ||||||
| chr12:9180405
|
T | C | 2 | a0006c0007t0001g0036a0006c0007t0001g0222 | 2 | NA18961.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1839+578A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180405 | ||||||
| chr12:9180520
|
G | A | 1 | a0012c0024t0001g0251 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1839+463C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180520 | ||||||
| chr12:9180724
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1839+259G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180724 | ||||||
| chr12:9180745
|
G | A | 1 | a0008c0039t0001g0069 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1839+238C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180745 | ||||||
| chr12:9180799
|
T | C | 1 | a0016c0016t0001g0140 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1839+184A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180799 | ||||||
| chr12:9180821
|
G | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(171): Show | 209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1839+162C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180821 | ||||||
| chr12:9180848
|
T | A | 2 | a0003c0022t0001g0236a0003c0022t0001g0239 | 2 | HG00639.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1839+135A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180848 | ||||||
| chr12:9180872
|
A | C | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1839+111T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180872 | ||||||
| chr12:9180889
|
G | A | 5 | a0008c0020t0001g0032a0008c0020t0001g0270a0008c0039t0001g0069others(2): Show | 6 | HG02258.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1839+94C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 15/35 | chr12 | 9180889 | ||||||
| chr12:9181153
|
G | A | 92 | a0001c0001t0001g0038a0001c0001t0001g0081a0001c0001t0001g0125others(89): Show | 102 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.1690-21C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181153 | ||||||
| chr12:9181311
|
C | T | 26 | a0001c0055t0001g0214a0003c0003t0001g0019a0003c0003t0001g0042others(23): Show | 27 | HG00280.hp2 HG01109.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1690-179G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181311 | ||||||
| chr12:9181375
|
T | C | 1 | a0006c0007t0001g0256 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1690-243A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181375 | ||||||
| chr12:9181658
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1689+317C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181658 | ||||||
| chr12:9181725
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1689+250G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181725 | ||||||
| chr12:9181903
|
T | C | 1 | a0003c0003t0001g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1689+72A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181903 | ||||||
| chr12:9181905
|
T | C | 1 | a0003c0003t0001g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1689+70A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181905 | ||||||
| chr12:9181961
|
G | A | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1689+14C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 14/35 | chr12 | 9181961 | ||||||
| chr12:9182132
|
G | GAGTGAGA others(13): Show |
197 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(194): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1547-35_1547-16dup others(20): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182132 | ||||||
| chr12:9182198
|
G | T | 1 | a0026c0051t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1547-81C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182198 | ||||||
| chr12:9182225
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1547-108C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182225 | ||||||
| chr12:9182419
|
C | CAT | 208 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(205): Show | 248 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1547-304_1547-303d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182419 | ||||||
| chr12:9182636
|
T | C | 82 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(79): Show | 92 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1547-519A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182636 | ||||||
| chr12:9182678
|
A | C | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1547-561T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182678 | ||||||
| chr12:9182712
|
G | A | 3 | a0003c0003t0001g0200a0003c0003t0001g0203a0021c0028t0001g0204 | 3 | HG01109.hp2 HG01891.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1547-595C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182712 | ||||||
| chr12:9182743
|
C | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(160): Show | 198 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1547-626G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182743 | ||||||
| chr12:9182820
|
A | T | 34 | a0001c0055t0001g0214a0003c0003t0001g0002a0003c0003t0001g0019others(31): Show | 38 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1547-703T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182820 | ||||||
| chr12:9182901
|
C | T | 1 | a0001c0013t0001g0278 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1547-784G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9182901 | ||||||
| chr12:9183050
|
C | T | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1547-933G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183050 | ||||||
| chr12:9183156
|
A | G | 34 | a0001c0055t0001g0214a0003c0003t0001g0002a0003c0003t0001g0019others(31): Show | 38 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1547-1039T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183156 | ||||||
| chr12:9183321
|
G | T | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1547-1204C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183321 | ||||||
| chr12:9183408
|
A | AT | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(154): Show | 192 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1547-1292dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183408 | ||||||
| chr12:9183630
|
C | T | 1 | a0010c0009t0001g0101 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1547-1513G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183630 | ||||||
| chr12:9183685
|
G | A | 2 | a0007c0005t0001g0071a0007c0005t0001g0072 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1547-1568C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183685 | ||||||
| chr12:9183772
|
G | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(272): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1547-1655C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183772 | ||||||
| chr12:9183822
|
A | G | 82 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(79): Show | 92 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1547-1705T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183822 | ||||||
| chr12:9183905
|
T | C | 9 | a0002c0002t0001g0130a0002c0002t0001g0151a0002c0002t0001g0154others(6): Show | 9 | HG00738.hp2 HG01168.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1547-1788A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9183905 | ||||||
| chr12:9184136
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0083a0009c0006t0001g0070others(1): Show | 5 | HG02135.hp2 NA18961.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1547-2019A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184136 | ||||||
| chr12:9184223
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1547-2106C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184223 | ||||||
| chr12:9184347
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1547-2230C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184347 | ||||||
| chr12:9184423
|
C | T | 1 | a0006c0007t0001g0247 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1547-2306G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184423 | ||||||
| chr12:9184561
|
G | A | 2 | a0003c0003t0001g0205a0003c0022t0001g0121 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1547-2444C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184561 | ||||||
| chr12:9184713
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1547-2596G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184713 | ||||||
| chr12:9184972
|
G | T | 1 | a0001c0001t0001g0059 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1547-2855C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9184972 | ||||||
| chr12:9185072
|
A | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(185): Show | 226 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1547-2955T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185072 | ||||||
| chr12:9185391
|
T | C | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1547-3274A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185391 | ||||||
| chr12:9185658
|
GAA | G | 233 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(230): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1547-3543_1547-354 others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185658 | ||||||
| chr12:9185672
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1547-3555C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185672 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(3): Show |
3 | a0002c0002t0001g0154a0002c0002t0001g0217a0017c0018t0001g0169 | 3 | HG01256.hp2 HG02080.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1547-3683_1547-367 others(14): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(8): Show |
12 | a0001c0001t0001g0074a0002c0002t0001g0117a0002c0002t0001g0130others(9): Show | 12 | HG01433.hp2 HG02717.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.1547-3688_1547-367 others(19): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(13): Show |
51 | a0001c0001t0001g0073a0001c0021t0001g0193a0002c0002t0001g0003others(48): Show | 57 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1547-3693_1547-367 others(24): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(18): Show |
49 | a0001c0038t0001g0119a0001c0046t0001g0050a0002c0002t0001g0145others(46): Show | 60 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1547-3698_1547-367 others(29): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(23): Show |
24 | a0001c0001t0001g0028a0001c0026t0001g0034a0001c0026t0001g0126others(21): Show | 26 | HG00609.hp1 HG00639.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(34): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(28): Show |
9 | a0004c0004t0001g0245a0006c0007t0001g0036a0006c0007t0001g0222others(6): Show | 9 | HG01074.hp1 HG02074.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(39): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(33): Show |
4 | a0001c0021t0001g0123a0008c0020t0001g0032a0008c0020t0001g0270others(1): Show | 5 | HG01993.hp1 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(44): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(38): Show |
3 | a0001c0013t0001g0278a0020c0027t0001g0027a0023c0050t0001g0168 | 4 | HG02145.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(49): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(48): Show |
1 | a0001c0013t0001g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1547-3674_1547-367 others(59): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(53): Show |
3 | a0001c0013t0001g0277a0001c0013t0001g0279a0001c0059t0001g0197 | 3 | HG02572.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1547-3674_1547-367 others(64): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185790
|
A | ATTTCTTT others(58): Show |
1 | a0001c0013t0001g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1547-3674_1547-367 others(69): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185790 | ||||||
| chr12:9185814
|
C | CTTTTCTT others(19): Show |
1 | a0005c0008t0001g0190 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1547-3698_1547-369 others(30): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185814 | ||||||
| chr12:9185815
|
T | TTTTCTTT others(22): Show |
1 | a0007c0005t0001g0271 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1547-3699_1547-369 others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185815 | ||||||
| chr12:9185819
|
T | C | 1 | a0010c0009t0001g0244 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1547-3702A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185819 | ||||||
| chr12:9185938
|
G | A | 2 | a0016c0016t0001g0155a0016c0016t0001g0156 | 2 | HG00099.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1547-3821C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185938 | ||||||
| chr12:9185953
|
G | A | 1 | a0004c0004t0001g0265 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1547-3836C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9185953 | ||||||
| chr12:9186020
|
A | C | 1 | a0001c0001t0001g0013 | 2 | NA18942.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1547-3903T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186020 | ||||||
| chr12:9186039
|
T | C | 1 | a0006c0007t0001g0232 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1547-3922A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186039 | ||||||
| chr12:9186059
|
A | G | 165 | a0001c0001t0001g0028a0001c0001t0001g0073a0001c0001t0001g0074others(162): Show | 187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1547-3942T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186059 | ||||||
| chr12:9186067
|
A | G | 1 | a0002c0002t0001g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1547-3950T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186067 | ||||||
| chr12:9186079
|
T | A | 1 | a0007c0005t0001g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1547-3962A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186079 | ||||||
| chr12:9186113
|
T | G | 1 | a0002c0002t0001g0158 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1547-3996A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186113 | ||||||
| chr12:9186143
|
C | A | 1 | a0026c0051t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1547-4026G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186143 | ||||||
| chr12:9186264
|
G | A | 1 | a0004c0004t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1547-4147C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186264 | ||||||
| chr12:9186383
|
G | T | 6 | a0010c0009t0001g0012a0010c0009t0001g0223a0010c0009t0001g0229others(3): Show | 8 | HG01106.hp2 HG01109.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1547-4266C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186383 | ||||||
| chr12:9186429
|
T | C | 3 | a0001c0001t0001g0017a0009c0006t0001g0070a0009c0006t0001g0084 | 4 | HG02135.hp2 NA18961.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-4312A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186429 | ||||||
| chr12:9186543
|
T | A | 1 | a0006c0007t0001g0252 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1547-4426A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186543 | ||||||
| chr12:9186603
|
C | A | 153 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(150): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1547-4486G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186603 | ||||||
| chr12:9186688
|
C | A | 4 | a0003c0003t0001g0002a0003c0003t0001g0102a0003c0003t0001g0103others(1): Show | 7 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-4571G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186688 | ||||||
| chr12:9186859
|
G | A | 1 | a0003c0022t0001g0239 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1547-4742C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186859 | ||||||
| chr12:9186904
|
A | G | 85 | a0001c0021t0001g0123a0002c0002t0001g0003a0002c0002t0001g0010others(82): Show | 94 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1547-4787T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9186904 | ||||||
| chr12:9187048
|
G | A | 1 | a0001c0046t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1547-4931C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187048 | ||||||
| chr12:9187077
|
C | CAA | 80 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(77): Show | 89 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1547-4962_1547-496 others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187077 | ||||||
| chr12:9187077
|
CA | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(141): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1547-4961delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187077 | ||||||
| chr12:9187215
|
A | G | 3 | a0003c0003t0001g0095a0003c0003t0001g0097a0003c0003t0001g0105 | 3 | HG02965.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1546+4978T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187215 | ||||||
| chr12:9187226
|
A | G | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4967T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187226 | ||||||
| chr12:9187408
|
C | A | 1 | a0013c0011t0001g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1546+4785G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187408 | ||||||
| chr12:9187413
|
A | G | 51 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(48): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1546+4780T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187413 | ||||||
| chr12:9187672
|
A | G | 85 | a0001c0021t0001g0123a0002c0002t0001g0003a0002c0002t0001g0010others(82): Show | 94 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1546+4521T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187672 | ||||||
| chr12:9187681
|
G | A | 5 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546+4512C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187681 | ||||||
| chr12:9187693
|
G | A | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1546+4500C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187693 | ||||||
| chr12:9187762
|
G | A | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4431C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187762 | ||||||
| chr12:9187816
|
C | G | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1546+4377G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187816 | ||||||
| chr12:9187882
|
C | A | 1 | a0011c0010t0001g0110 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1546+4311G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9187882 | ||||||
| chr12:9188000
|
A | C | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4193T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188000 | ||||||
| chr12:9188033
|
G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG00408.hp1 NA19004.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+4160C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188033 | ||||||
| chr12:9188046
|
G | A | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1546+4147C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188046 | ||||||
| chr12:9188108
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(233): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1546+4085A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188108 | ||||||
| chr12:9188113
|
C | T | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+4080G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188113 | ||||||
| chr12:9188445
|
C | T | 6 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+3748G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188445 | ||||||
| chr12:9188559
|
C | A | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+3634G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188559 | ||||||
| chr12:9188832
|
A | T | 1 | a0006c0029t0001g0057 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1546+3361T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9188832 | ||||||
| chr12:9189016
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1546+3177T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189016 | ||||||
| chr12:9189117
|
C | T | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+3076G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189117 | ||||||
| chr12:9189333
|
T | G | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+2860A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189333 | ||||||
| chr12:9189447
|
G | T | 88 | a0001c0021t0001g0123a0001c0021t0001g0193a0001c0038t0001g0119others(85): Show | 97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546+2746C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189447 | ||||||
| chr12:9189690
|
T | C | 1 | a0017c0018t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1546+2503A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189690 | ||||||
| chr12:9189924
|
A | G | 88 | a0001c0021t0001g0123a0001c0021t0001g0193a0001c0038t0001g0119others(85): Show | 97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546+2269T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9189924 | ||||||
| chr12:9190063
|
C | G | 1 | a0006c0035t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1546+2130G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190063 | ||||||
| chr12:9190227
|
A | G | 1 | a0002c0002t0001g0184 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1546+1966T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190227 | ||||||
| chr12:9190254
|
C | T | 6 | a0003c0003t0001g0019a0003c0003t0001g0042a0003c0003t0001g0054others(3): Show | 7 | NA18953.hp1 NA18970.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+1939G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190254 | ||||||
| chr12:9190294
|
C | T | 152 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(149): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1546+1899G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190294 | ||||||
| chr12:9190422
|
C | T | 3 | a0001c0021t0001g0193a0001c0038t0001g0119a0023c0050t0001g0168 | 3 | HG02055.hp1 HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1546+1771G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190422 | ||||||
| chr12:9190488
|
C | T | 2 | a0007c0005t0001g0071a0007c0005t0001g0072 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1546+1705G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190488 | ||||||
| chr12:9190696
|
T | C | 1 | a0009c0006t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1546+1497A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190696 | ||||||
| chr12:9190726
|
A | T | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1546+1467T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190726 | ||||||
| chr12:9190908
|
T | C | 6 | a0001c0026t0001g0034a0001c0026t0001g0126a0008c0020t0001g0032others(3): Show | 7 | HG02258.hp2 HG02280.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+1285A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190908 | ||||||
| chr12:9190924
|
G | C | 1 | a0030c0044t0001g0255 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546+1269C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190924 | ||||||
| chr12:9190989
|
A | T | 2 | a0002c0002t0001g0010a0002c0002t0001g0139 | 4 | HG01081.hp2 HG01192.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+1204T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190989 | ||||||
| chr12:9190990
|
T | G | 88 | a0001c0021t0001g0123a0001c0021t0001g0193a0001c0038t0001g0119others(85): Show | 97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546+1203A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9190990 | ||||||
| chr12:9191057
|
A | T | 6 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546+1136T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191057 | ||||||
| chr12:9191297
|
G | A | 1 | a0002c0002t0001g0094 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1546+896C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191297 | ||||||
| chr12:9191403
|
A | T | 2 | a0007c0005t0001g0071a0007c0005t0001g0072 | 2 | HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1546+790T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191403 | ||||||
| chr12:9191778
|
C | A | 1 | a0008c0020t0001g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1546+415G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 13/35 | chr12 | 9191778 | ||||||
| chr12:9192282
|
A | G | 86 | a0001c0021t0001g0123a0002c0002t0001g0003a0002c0002t0001g0010others(83): Show | 95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1483-26T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 12/35 | chr12 | 9192282 | ||||||
| chr12:9192366
|
A | G | 51 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(48): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1483-110T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 12/35 | chr12 | 9192366 | ||||||
| chr12:9192754
|
A | G | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1255-15T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192754 | ||||||
| chr12:9192784
|
T | G | 1 | a0007c0005t0001g0018 | 2 | HG01516.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1255-45A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192784 | ||||||
| chr12:9192812
|
A | G | 156 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(153): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1255-73T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192812 | ||||||
| chr12:9192868
|
G | A | 1 | a0003c0041t0001g0088 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1255-129C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9192868 | ||||||
| chr12:9193054
|
C | G | 1 | a0011c0010t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1255-315G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193054 | ||||||
| chr12:9193221
|
T | C | 156 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0089others(153): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1255-482A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193221 | ||||||
| chr12:9193226
|
G | A | 86 | a0001c0021t0001g0123a0002c0002t0001g0003a0002c0002t0001g0010others(83): Show | 95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1255-487C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193226 | ||||||
| chr12:9193506
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(233): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1254+571A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193506 | ||||||
| chr12:9193606
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(269): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1254+471A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193606 | ||||||
| chr12:9193696
|
C | T | 3 | a0001c0021t0001g0193a0001c0038t0001g0119a0023c0050t0001g0168 | 3 | HG02055.hp1 HG02145.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1254+381G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193696 | ||||||
| chr12:9193727
|
G | A | 5 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+350C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193727 | ||||||
| chr12:9193869
|
ATGAT | A | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+204_1254+207d others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193869 | ||||||
| chr12:9193875
|
G | A | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+202C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193875 | ||||||
| chr12:9193877
|
GAAA | G | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+197_1254+199d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193877 | ||||||
| chr12:9193883
|
ATCAGGCA others(3): Show |
A | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+184_1254+193d others(12): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193883 | ||||||
| chr12:9193895
|
T | A | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+182A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193895 | ||||||
| chr12:9193897
|
C | T | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+180G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193897 | ||||||
| chr12:9193899
|
G | A | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+178C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193899 | ||||||
| chr12:9193900
|
T | A | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+177A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193900 | ||||||
| chr12:9193902
|
C | G | 6 | a0002c0002t0001g0046a0002c0002t0001g0137a0002c0002t0001g0144others(3): Show | 6 | NA18963.hp1 NA18984.hp2 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+175G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 11/35 | chr12 | 9193902 | ||||||
| chr12:9194297
|
A | T | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1093-59T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194297 | ||||||
| chr12:9194318
|
G | T | 1 | a0004c0004t0001g0275 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1093-80C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194318 | ||||||
| chr12:9194462
|
G | GT | 7 | a0001c0055t0001g0214a0003c0003t0001g0102a0003c0003t0001g0266others(4): Show | 7 | HG01175.hp1 HG02630.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1093-225dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194462 | ||||||
| chr12:9194462
|
GT | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(202): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1093-225delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194462 | ||||||
| chr12:9194474
|
T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1093-236A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194474 | ||||||
| chr12:9194475
|
T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1093-237A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194475 | ||||||
| chr12:9194560
|
A | G | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1093-322T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194560 | ||||||
| chr12:9194561
|
C | T | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1093-323G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194561 | ||||||
| chr12:9194564
|
A | C | 1 | a0003c0003t0001g0199 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1093-326T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194564 | ||||||
| chr12:9194580
|
T | G | 1 | a0002c0002t0001g0136 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1093-342A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194580 | ||||||
| chr12:9194603
|
T | C | 2 | a0001c0001t0001g0043a0007c0005t0001g0044 | 2 | HG02155.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1093-365A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194603 | ||||||
| chr12:9194638
|
G | A | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1093-400C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194638 | ||||||
| chr12:9194745
|
T | A | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1093-507A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194745 | ||||||
| chr12:9194798
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1093-560G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9194798 | ||||||
| chr12:9195143
|
A | G | 1 | a0035c0061t0001g0142 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1093-905T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195143 | ||||||
| chr12:9195180
|
A | G | 1 | a0007c0005t0001g0243 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1093-942T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195180 | ||||||
| chr12:9195295
|
A | T | 1 | a0004c0004t0001g0233 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1092+1035T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195295 | ||||||
| chr12:9195443
|
C | G | 1 | a0004c0004t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1092+887G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195443 | ||||||
| chr12:9195611
|
A | AT | 64 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0056others(61): Show | 77 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.1092+718dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195611 | ||||||
| chr12:9195611
|
A | ATT | 12 | a0004c0004t0001g0225a0004c0004t0001g0233a0004c0004t0001g0234others(9): Show | 13 | HG00642.hp2 HG01346.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.1092+717_1092+718d others(4): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195611 | ||||||
| chr12:9195611
|
AT | A | 7 | a0001c0001t0001g0053a0001c0013t0001g0279a0001c0021t0001g0193others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1092+718delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195611 | ||||||
| chr12:9195629
|
T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092+701A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195629 | ||||||
| chr12:9195702
|
C | G | 82 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(79): Show | 91 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1092+628G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195702 | ||||||
| chr12:9195730
|
A | G | 1 | a0002c0002t0001g0137 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1092+600T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195730 | ||||||
| chr12:9195736
|
G | A | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1092+594C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195736 | ||||||
| chr12:9195756
|
A | G | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1092+574T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195756 | ||||||
| chr12:9195824
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1092+506A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195824 | ||||||
| chr12:9195845
|
A | G | 1 | a0010c0054t0001g0221 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1092+485T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195845 | ||||||
| chr12:9195867
|
TATA | T | 88 | a0001c0021t0001g0123a0001c0021t0001g0193a0001c0038t0001g0119others(85): Show | 97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1092+460_1092+462d others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195867 | ||||||
| chr12:9195903
|
A | T | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092+427T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195903 | ||||||
| chr12:9195904
|
T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1092+426A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9195904 | ||||||
| chr12:9196019
|
G | A | 1 | a0004c0004t0001g0224 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1092+311C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 10/35 | chr12 | 9196019 | ||||||
| chr12:9196687
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG01496.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.868-2A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196687 | ||||||
| chr12:9196774
|
C | CT | 153 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(150): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.868-90dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196774 | ||||||
| chr12:9196808
|
C | T | 12 | a0001c0001t0001g0116a0001c0046t0001g0050a0003c0022t0001g0236others(9): Show | 13 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.868-123G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196808 | ||||||
| chr12:9196891
|
C | A | 3 | a0008c0020t0001g0032a0008c0020t0001g0270a0024c0036t0001g0231 | 4 | HG02258.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+121G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196891 | ||||||
| chr12:9196892
|
G | A | 1 | a0015c0017t0001g0026 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.867+120C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196892 | ||||||
| chr12:9196970
|
T | C | 4 | a0003c0003t0001g0002a0003c0003t0001g0102a0003c0003t0001g0103others(1): Show | 7 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.867+42A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 8/35 | chr12 | 9196970 | ||||||
| chr12:9197139
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.756-16A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197139 | ||||||
| chr12:9197359
|
A | G | 89 | a0001c0021t0001g0123a0001c0021t0001g0193a0001c0038t0001g0119others(86): Show | 98 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.756-236T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197359 | ||||||
| chr12:9197416
|
A | G | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.756-293T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197416 | ||||||
| chr12:9197418
|
TAAAATAA others(93): Show |
T | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.756-395_756-296del others(100): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197418 | ||||||
| chr12:9197425
|
A | C | 47 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(44): Show | 56 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.756-302T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197425 | ||||||
| chr12:9197480
|
TATA | T | 6 | a0001c0013t0001g0111a0001c0013t0001g0276a0001c0013t0001g0277others(3): Show | 7 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.756-360_756-358del others(3): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197480 | ||||||
| chr12:9197595
|
TA | T | 60 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(57): Show | 71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.756-473delT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197595 | ||||||
| chr12:9197606
|
T | C | 1 | a0005c0008t0001g0182 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.756-483A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197606 | ||||||
| chr12:9197611
|
T | G | 1 | a0023c0050t0001g0168 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.756-488A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197611 | ||||||
| chr12:9197632
|
A | C | 3 | a0003c0003t0001g0019a0003c0003t0001g0042a0003c0003t0001g0054 | 4 | NA18970.hp2 NA18974.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-509T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197632 | ||||||
| chr12:9197632
|
ATATATTA others(3): Show |
A | 3 | a0001c0026t0001g0034a0001c0026t0001g0126a0028c0042t0001g0162 | 3 | HG02280.hp1 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.756-519_756-510del others(10): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197632 | ||||||
| chr12:9197642
|
T | TTA | 149 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(146): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.756-521_756-520dup others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197642 | ||||||
| chr12:9197643
|
T | A | 7 | a0011c0010t0001g0021a0011c0010t0001g0035a0011c0010t0001g0107others(4): Show | 8 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.756-520A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197643 | ||||||
| chr12:9197643
|
TATATAAT others(3): Show |
T | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.756-530_756-521del others(10): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197643 | ||||||
| chr12:9197649
|
A | T | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.756-526T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197649 | ||||||
| chr12:9197650
|
T | A | 1 | a0002c0002t0001g0159 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.756-527A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197650 | ||||||
| chr12:9197663
|
TATTATAT others(26): Show |
T | 4 | a0006c0007t0001g0230a0008c0020t0001g0032a0008c0020t0001g0270others(1): Show | 5 | HG02074.hp2 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.756-573_756-541del others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197663 | ||||||
| chr12:9197667
|
ATATATAT others(24): Show |
A | 169 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(166): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.756-575_756-545del others(31): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197667 | ||||||
| chr12:9197684
|
C | T | 11 | a0001c0001t0001g0031a0004c0004t0001g0225a0004c0004t0001g0260others(8): Show | 12 | HG01070.hp1 HG01071.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.756-561G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197684 | ||||||
| chr12:9197715
|
C | T | 54 | a0001c0001t0001g0028a0001c0001t0001g0116a0001c0013t0001g0111others(51): Show | 65 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.756-592G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197715 | ||||||
| chr12:9197715
|
CATAATAT others(117): Show |
C | 4 | a0001c0021t0001g0123a0003c0022t0001g0121a0007c0005t0001g0122others(1): Show | 4 | HG01993.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-716_756-593del | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197715 | ||||||
| chr12:9197718
|
AATATATA others(26): Show |
A | 1 | a0011c0010t0001g0021 | 2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.756-628_756-596del others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197718 | ||||||
| chr12:9197726
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA19067.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.756-603A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197726 | ||||||
| chr12:9197777
|
CATAATAT others(55): Show |
C | 78 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0046others(75): Show | 87 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.756-716_756-655del others(62): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197777 | ||||||
| chr12:9197780
|
AATATATA others(26): Show |
A | 1 | a0001c0031t0001g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-690_756-658del others(33): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197780 | ||||||
| chr12:9197808
|
CATAATAT others(24): Show |
C | 4 | a0002c0002t0001g0130a0002c0002t0001g0137a0002c0065t0001g0138others(1): Show | 4 | HG00621.hp2 HG00673.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.756-716_756-686del others(31): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197808 | ||||||
| chr12:9197826
|
A | G | 1 | a0010c0009t0001g0229 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.756-703T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197826 | ||||||
| chr12:9197934
|
ATATAT | A | 4 | a0001c0021t0001g0123a0003c0022t0001g0121a0007c0005t0001g0122others(1): Show | 4 | HG01993.hp1 HG02145.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.756-816_756-812del others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9197934 | ||||||
| chr12:9198045
|
CAT | C | 155 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(152): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.756-924_756-923del others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198045 | ||||||
| chr12:9198178
|
A | G | 155 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(152): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.756-1055T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198178 | ||||||
| chr12:9198258
|
A | G | 4 | a0015c0017t0001g0025a0015c0017t0001g0026a0015c0017t0001g0219others(1): Show | 6 | HG01884.hp2 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.756-1135T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198258 | ||||||
| chr12:9198473
|
A | G | 86 | a0001c0021t0001g0123a0002c0002t0001g0003a0002c0002t0001g0010others(83): Show | 95 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.756-1350T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9198473 | ||||||
| chr12:9199050
|
A | G | 2 | a0014c0015t0001g0128a0014c0015t0001g0129 | 2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.755+1314T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199050 | ||||||
| chr12:9199052
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(255): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.755+1312T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199052 | ||||||
| chr12:9199414
|
A | G | 1 | a0012c0014t0001g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755+950T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199414 | ||||||
| chr12:9199625
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.755+739G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199625 | ||||||
| chr12:9199725
|
T | C | 1 | a0001c0026t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.755+639A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199725 | ||||||
| chr12:9199756
|
T | C | 1 | a0026c0051t0001g0207 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.755+608A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199756 | ||||||
| chr12:9199863
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(100): Show | 132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.755+501C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199863 | ||||||
| chr12:9199881
|
A | G | 52 | a0001c0021t0001g0123a0001c0026t0001g0126a0002c0002t0001g0003others(49): Show | 57 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.755+483T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199881 | ||||||
| chr12:9199887
|
A | G | 1 | a0001c0001t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.755+477T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9199887 | ||||||
| chr12:9200047
|
A | G | 6 | a0011c0010t0001g0021a0011c0010t0001g0035a0011c0010t0001g0107others(3): Show | 7 | HG01884.hp1 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+317T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200047 | ||||||
| chr12:9200117
|
C | T | 44 | a0002c0002t0001g0003a0002c0002t0001g0010a0002c0002t0001g0130others(41): Show | 49 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.755+247G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200117 | ||||||
| chr12:9200194
|
T | C | 1 | a0002c0002t0001g0163 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.755+170A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200194 | ||||||
| chr12:9200195
|
A | G | 13 | a0001c0001t0001g0198a0001c0001t0001g0206a0001c0055t0001g0214others(10): Show | 13 | HG00280.hp2 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.755+169T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200195 | ||||||
| chr12:9200312
|
C | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(221): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.755+52G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200312 | ||||||
| chr12:9200349
|
A | C | 5 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0186others(2): Show | 5 | HG00642.hp1 HG01081.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+15T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 7/35 | chr12 | 9200349 | ||||||
| chr12:9200569
|
A | G | 3 | a0001c0001t0001g0043a0003c0003t0001g0042a0007c0005t0001g0044 | 3 | HG02155.hp1 NA18970.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.671-121T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 6/35 | chr12 | 9200569 | ||||||
| chr12:9200636
|
C | T | 1 | a0001c0059t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.671-188G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 6/35 | chr12 | 9200636 | ||||||
| chr12:9201232
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 133 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.501+95T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 5/35 | chr12 | 9201232 | ||||||
| chr12:9201279
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 133 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.501+48A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 5/35 | chr12 | 9201279 | ||||||
| chr12:9201690
|
T | G | 1 | a0017c0018t0001g0166 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.481-343A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201690 | ||||||
| chr12:9201757
|
A | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 133 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.481-410T>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201757 | ||||||
| chr12:9201817
|
C | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 133 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.481-470G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201817 | ||||||
| chr12:9201921
|
C | T | 1 | a0002c0002t0001g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480+398G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201921 | ||||||
| chr12:9201988
|
G | T | 257 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(254): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.480+331C>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9201988 | ||||||
| chr12:9202125
|
T | A | 1 | a0027c0052t0001g0106 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480+194A>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9202125 | ||||||
| chr12:9202249
|
C | A | 1 | a0001c0021t0001g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.480+70G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 4/35 | chr12 | 9202249 | ||||||
| chr12:9202424
|
G | C | 1 | a0001c0021t0001g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.428-53C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 3/35 | chr12 | 9202424 | ||||||
| chr12:9202792
|
G | C | 1 | a0013c0011t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.268-108C>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9202792 | ||||||
| chr12:9202892
|
A | G | 1 | a0017c0018t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268-208T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9202892 | ||||||
| chr12:9203017
|
G | A | 1 | a0002c0002t0001g0164 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.268-333C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203017 | ||||||
| chr12:9203265
|
T | TA | 63 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(60): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.267+502dupT | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203265 | ||||||
| chr12:9203271
|
A | T | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.267+497T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203271 | ||||||
| chr12:9203318
|
T | C | 1 | a0001c0026t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.267+450A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203318 | ||||||
| chr12:9203337
|
C | CT | 29 | a0001c0001t0001g0183a0001c0038t0001g0119a0002c0002t0001g0130others(26): Show | 31 | HG00280.hp2 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.267+430dupA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | ||||||
| chr12:9203337
|
CT | C | 13 | a0001c0013t0001g0276a0001c0013t0001g0277a0001c0013t0001g0278others(10): Show | 14 | HG00738.hp2 HG01106.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.267+430delA | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | ||||||
| chr12:9203337
|
CTT | C | 55 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0116others(52): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.267+429_267+430del others(2): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | ||||||
| chr12:9203337
|
CTTT | C | 5 | a0007c0005t0001g0033a0007c0005t0001g0271a0008c0020t0001g0032others(2): Show | 7 | HG02083.hp1 HG02647.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+428_267+430del others(3): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | ||||||
| chr12:9203337
|
CTTTTT | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(71): Show | 97 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.267+426_267+430del others(5): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | ||||||
| chr12:9203337
|
CTTTTTT | C | 25 | a0001c0001t0001g0020a0001c0013t0001g0111a0002c0002t0001g0094others(22): Show | 31 | HG01884.hp1 HG02015.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.267+425_267+430del others(6): Show |
PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203337 | ||||||
| chr12:9203368
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(99): Show | 131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.267+400C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203368 | ||||||
| chr12:9203451
|
C | T | 2 | a0017c0018t0001g0169a0017c0018t0001g0170 | 2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.267+317G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203451 | ||||||
| chr12:9203502
|
C | T | 1 | a0017c0018t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.267+266G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203502 | ||||||
| chr12:9203524
|
G | A | 7 | a0001c0013t0001g0111a0011c0010t0001g0021a0011c0010t0001g0035others(4): Show | 8 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+244C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203524 | ||||||
| chr12:9203563
|
G | A | 31 | a0001c0001t0001g0183a0001c0001t0001g0192a0001c0021t0001g0193others(28): Show | 35 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.267+205C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 2/35 | chr12 | 9203563 | ||||||
| chr12:9204007
|
T | C | 33 | a0001c0001t0001g0183a0001c0001t0001g0192a0001c0021t0001g0193others(30): Show | 37 | HG00423.hp1 HG00621.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.84-56A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204007 | ||||||
| chr12:9204063
|
A | G | 1 | a0001c0026t0001g0126 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.84-112T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204063 | ||||||
| chr12:9204085
|
T | G | 1 | a0001c0055t0001g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.84-134A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204085 | ||||||
| chr12:9204156
|
T | C | 1 | a0007c0005t0001g0273 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.84-205A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204156 | ||||||
| chr12:9204340
|
A | T | 1 | a0006c0007t0001g0036 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.84-389T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204340 | ||||||
| chr12:9204410
|
C | T | 5 | a0001c0001t0001g0125a0001c0021t0001g0123a0003c0022t0001g0121others(2): Show | 5 | HG01891.hp2 HG01993.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.84-459G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204410 | ||||||
| chr12:9204844
|
C | T | 2 | a0001c0013t0001g0276a0001c0013t0001g0277 | 2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.84-893G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204844 | ||||||
| chr12:9204854
|
G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(1): Show | 4 | HG00408.hp1 NA19004.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-903C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204854 | ||||||
| chr12:9204906
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(100): Show | 132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.84-955T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204906 | ||||||
| chr12:9204981
|
C | T | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(100): Show | 132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.84-1030G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9204981 | ||||||
| chr12:9205139
|
T | C | 1 | a0002c0002t0001g0117 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.84-1188A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205139 | ||||||
| chr12:9205223
|
AC | A | 4 | a0001c0013t0001g0276a0001c0013t0001g0277a0001c0013t0001g0278others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-1273delG | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205223 | ||||||
| chr12:9205271
|
C | T | 1 | a0011c0010t0001g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.84-1320G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205271 | ||||||
| chr12:9205330
|
C | G | 1 | a0017c0018t0001g0120 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.84-1379G>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205330 | ||||||
| chr12:9205543
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(255): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.84-1592T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205543 | ||||||
| chr12:9205622
|
A | G | 1 | a0020c0027t0001g0027 | 2 | HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.84-1671T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205622 | ||||||
| chr12:9205627
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.84-1676C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205627 | ||||||
| chr12:9205676
|
T | C | 1 | a0006c0007t0001g0118 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.84-1725A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205676 | ||||||
| chr12:9205677
|
T | C | 1 | a0004c0004t0001g0274 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.84-1726A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205677 | ||||||
| chr12:9205702
|
A | G | 53 | a0001c0001t0001g0125a0001c0021t0001g0123a0001c0026t0001g0126others(50): Show | 58 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.84-1751T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205702 | ||||||
| chr12:9205878
|
A | T | 1 | a0001c0038t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.84-1927T>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9205878 | ||||||
| chr12:9206152
|
G | A | 3 | a0002c0002t0001g0215a0002c0002t0001g0217a0005c0008t0001g0216 | 3 | HG02080.hp2 NA19000.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.83+2107C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206152 | ||||||
| chr12:9206185
|
T | C | 4 | a0015c0017t0001g0025a0015c0017t0001g0026a0015c0017t0001g0219others(1): Show | 6 | HG01884.hp2 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+2074A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206185 | ||||||
| chr12:9206399
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(100): Show | 132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.83+1860T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206399 | ||||||
| chr12:9206476
|
T | G | 4 | a0001c0013t0001g0276a0001c0013t0001g0277a0001c0013t0001g0278others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+1783A>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206476 | ||||||
| chr12:9206648
|
T | C | 2 | a0004c0004t0001g0004a0004c0004t0001g0275 | 5 | HG00140.hp1 HG00280.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+1611A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206648 | ||||||
| chr12:9206783
|
T | C | 4 | a0001c0013t0001g0276a0001c0013t0001g0277a0001c0013t0001g0278others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.83+1476A>G | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206783 | ||||||
| chr12:9206887
|
C | T | 1 | a0010c0054t0001g0221 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.83+1372G>A | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206887 | ||||||
| chr12:9206976
|
A | G | 1 | a0001c0026t0001g0034 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83+1283T>C | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9206976 | ||||||
| chr12:9207613
|
C | A | 1 | a0009c0006t0001g0220 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.83+646G>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9207613 | ||||||
| chr12:9207884
|
G | A | 68 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0227others(65): Show | 80 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.83+375C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9207884 | ||||||
| chr12:9208210
|
G | A | 2 | a0013c0011t0001g0280a0013c0011t0001g0281 | 2 | HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.83+49C>T | PZP | ENSG00000126838.10 | transcript | ENST00000261336.7 | protein_coding | 1/35 | chr12 | 9208210 |