Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5829 |
|---|---|
| ensemblid | ENSG00000089159.17 |
| hgncid | 9718 |
| symbol | PXN |
| name | paxillin |
| refseq_nuc | NM_001385981.1 |
| refseq_prot | NP_001372910.1 |
| ensembl_nuc | ENST00000637617.2 |
| ensembl_prot | ENSP00000489840.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 120210447 |
| end | 120265730 |
| strand | - |
| ver | v1.2 |
| region | chr12:120210447-120265730 |
| region5000 | chr12:120205447-120270730 |
| regionname0 | PXN_chr12_120210447_120265730 |
| regionname5000 | PXN_chr12_120205447_120270730 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1081 | 253 | 61 | 33 | 125 | 4 | 29 | 89 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002 | 0/0 | 1081 | 38 | 25 | 11 | 0 | 1 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0003 | 1/0 | 1081 | 18 | 1 | 7 | 3 | 4 | 2 | 3 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0004 | 0/0 | 1081 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0005 | 0/0 | 1081 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0006 | 0/0 | 1081 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0007 | 0/0 | 1081 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0008 | 0/0 | 1081 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0009 | 0/0 | 1081 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0010 | 0/0 | 1081 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0011 | 0/0 | 1081 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0012 | 0/0 | 1081 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3246 | 216 | 30 | 30 | 124 | 4 | 27 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0002 | 0/0 | 3246 | 32 | 20 | 10 | 0 | 1 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0003 | 1/0 | 3246 | 18 | 1 | 7 | 3 | 4 | 2 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0004 | 0/0 | 3246 | 15 | 13 | 2 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0005 | 0/0 | 3246 | 5 | 5 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0006 | 0/0 | 3246 | 4 | 4 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0007 | 0/0 | 3246 | 4 | 0 | 0 | 4 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0008 | 0/0 | 3246 | 3 | 3 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0009 | 0/0 | 3246 | 2 | 0 | 0 | 1 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0010 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0011 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0012 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0013 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0014 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0015 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0016 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0017 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0018 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0019 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0020 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0021 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0022 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0023 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0024 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0025 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0026 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0027 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0028 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0029 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| c0030 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1969 | 206 | 70 | 31 | 80 | 7 | 16 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0002 | 0/0 | 1969 | 95 | 8 | 18 | 51 | 3 | 15 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0003 | 0/0 | 1970 | 10 | 9 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0004 | 0/0 | 1969 | 3 | 1 | 0 | 1 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0005 | 0/0 | 1969 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0006 | 0/0 | 1969 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0007 | 0/0 | 1969 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0008 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0009 | 0/0 | 1969 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0010 | 0/0 | 1969 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0011 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0012 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0013 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| t0014 | 0/0 | 1969 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0027 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3246 | 216 | 30 | 30 | 124 | 4 | 27 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0004 | 0/0 | 3246 | 15 | 13 | 2 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0005 | 0/0 | 3246 | 5 | 5 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0006 | 0/0 | 3246 | 4 | 4 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0010 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0013 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0014 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0017 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0018 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0022 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0023 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0024 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0025 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0029 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0030 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0002 | 0/0 | 3246 | 32 | 20 | 10 | 0 | 1 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0011 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0012 | 0/0 | 3246 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0019 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0026 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0003c0003 | 1/0 | 3246 | 18 | 1 | 7 | 3 | 4 | 2 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0004c0007 | 0/0 | 3246 | 4 | 0 | 0 | 4 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0005c0008 | 0/0 | 3246 | 3 | 3 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0006c0009 | 0/0 | 3246 | 2 | 0 | 0 | 1 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0007c0015 | 0/0 | 3246 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0008c0028 | 0/0 | 3246 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0009c0020 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0010c0027 | 0/0 | 3246 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0011c0021 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0012c0016 | 0/0 | 3246 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5214 | 109 | 14 | 9 | 72 | 1 | 12 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0002 | 0/0 | 5214 | 92 | 8 | 18 | 50 | 3 | 13 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0003 | 0/0 | 5215 | 8 | 7 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0005 | 0/0 | 5214 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0006 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0007 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0009 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0010 | 0/0 | 5214 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0011 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0001t0014 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0004t0001 | 0/0 | 5214 | 14 | 12 | 2 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0004t0008 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0005t0001 | 0/0 | 5214 | 5 | 5 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0006t0001 | 0/0 | 5214 | 4 | 4 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0010t0003 | 0/0 | 5215 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0013t0001 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0014t0001 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0017t0001 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0018t0002 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0022t0012 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0023t0001 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0024t0001 | 0/0 | 5214 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0025t0001 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0029t0002 | 0/0 | 5214 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0001c0030t0004 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0002t0001 | 0/0 | 5214 | 32 | 20 | 10 | 0 | 1 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0011t0001 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0012t0001 | 0/0 | 5214 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0019t0001 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0002c0026t0001 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0003c0003t0001 | 1/0 | 5214 | 18 | 1 | 7 | 3 | 4 | 2 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0004c0007t0001 | 0/0 | 5214 | 4 | 0 | 0 | 4 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0005c0008t0001 | 0/0 | 5214 | 3 | 3 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0006c0009t0004 | 0/0 | 5214 | 2 | 0 | 0 | 1 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0007c0015t0001 | 0/0 | 5214 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0008c0028t0001 | 0/0 | 5214 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0009c0020t0001 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0010c0027t0013 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0011c0021t0001 | 0/0 | 5214 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| a0012c0016t0002 | 0/0 | 5214 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | copy fasta | chr12 | 120205447 | 120270730 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0027 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0001t0014g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0004t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0006t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0010t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0010t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0013t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0013t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0014t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0017t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0018t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0022t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0023t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0024t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0025t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0029t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0001c0030t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0011t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0011t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0012t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0019t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0002c0026t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0114 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0003c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0004c0007t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0004c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0005c0008t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0005c0008t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0005c0008t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0006c0009t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0006c0009t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0007c0015t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0008c0028t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0009c0020t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0010c0027t0013g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0011c0021t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| a0012c0016t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | GBR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00140 | hp2 | a0003 | c0003 | t0001 | g0099 | EUR | GBR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0092 | EUR | FIN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0137 | EUR | FIN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00438 | hp2 | a0006 | c0009 | t0004 | g0034 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0100 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0101 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0086 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0107 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01106 | hp1 | a0001 | c0025 | t0001 | g0244 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0061 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0116 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0108 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0176 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0098 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0237 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01884 | hp1 | a0010 | c0027 | t0013 | g0282 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0072 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01928 | hp2 | a0008 | c0028 | t0001 | g0225 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0055 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01978 | hp2 | a0002 | c0026 | t0001 | g0235 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0236 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02027 | hp1 | a0001 | c0001 | t0009 | g0260 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02027 | hp2 | a0004 | c0007 | t0001 | g0262 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02055 | hp1 | a0001 | c0004 | t0001 | g0063 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02074 | hp2 | a0004 | c0007 | t0001 | g0008 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CDX | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CDX | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CDX | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02257 | hp2 | a0005 | c0008 | t0001 | g0268 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0059 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0050 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02451 | hp2 | a0001 | c0005 | t0001 | g0044 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0110 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0161 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0090 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0048 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02683 | hp1 | a0001 | c0029 | t0002 | g0122 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02683 | hp2 | a0003 | c0003 | t0001 | g0095 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02717 | hp1 | a0005 | c0008 | t0001 | g0258 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0047 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0083 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0051 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02809 | hp2 | a0001 | c0013 | t0001 | g0215 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0165 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02818 | hp2 | a0001 | c0013 | t0001 | g0213 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02886 | hp2 | a0002 | c0012 | t0001 | g0009 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02895 | hp1 | a0001 | c0004 | t0001 | g0043 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02895 | hp2 | a0002 | c0012 | t0001 | g0009 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02896 | hp2 | a0009 | c0020 | t0001 | g0045 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0156 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0060 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02965 | hp1 | a0001 | c0017 | t0001 | g0070 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02970 | hp2 | a0001 | c0010 | t0003 | g0211 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0280 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03041 | hp1 | a0001 | c0030 | t0004 | g0173 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0058 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0067 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0052 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03453 | hp1 | a0002 | c0011 | t0001 | g0080 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0091 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03486 | hp1 | a0002 | c0019 | t0001 | g0278 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03540 | hp1 | a0001 | c0006 | t0001 | g0038 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03540 | hp2 | a0001 | c0023 | t0001 | g0221 | AFR | GWD | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0174 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03710 | hp2 | a0001 | c0024 | t0001 | g0082 | SAS | PJL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | BEB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03927 | hp1 | a0006 | c0009 | t0004 | g0035 | SAS | BEB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG04204 | hp2 | a0012 | c0016 | t0002 | g0189 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0188 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0159 | AFR | YRI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0049 | AFR | YRI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18747 | hp1 | a0004 | c0007 | t0001 | g0008 | EAS | CHB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18906 | hp1 | a0001 | c0010 | t0003 | g0212 | AFR | YRI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18949 | hp1 | a0001 | c0001 | t0014 | g0283 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18952 | hp2 | a0001 | c0018 | t0002 | g0142 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0109 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18987 | hp1 | a0007 | c0015 | t0001 | g0120 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19030 | hp1 | a0001 | c0004 | t0008 | g0040 | AFR | LWK | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19030 | hp2 | a0002 | c0011 | t0001 | g0079 | AFR | LWK | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0256 | AFR | LWK | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19065 | hp1 | a0004 | c0007 | t0001 | g0008 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0115 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19240 | hp1 | a0001 | c0022 | t0012 | g0153 | AFR | YRI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | YRI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ASW | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | ASW | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0111 | EUR | TSI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20752 | hp2 | a0003 | c0003 | t0001 | g0102 | EUR | TSI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0112 | EUR | TSI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20805 | hp2 | a0011 | c0021 | t0001 | g0085 | EUR | TSI | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0088 | SAS | GIH | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | GIH | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0057 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02486 | hp1 | a0005 | c0008 | t0001 | g0259 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0169 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0039 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | ACB | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03471 | hp1 | a0001 | c0006 | t0001 | g0041 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG03471 | hp2 | a0001 | c0014 | t0001 | g0054 | AFR | MSL | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0042 | AFR | USA | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | USA | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | USA | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | USA | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0027 | REF | REF | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0114 | REF | REF | PXN_chr12_120205447_120270730 | PXN | chr12 | 120205447 | 120270730 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120216281
|
G | C | 3 | a0002a0008a0011 | 40 | HG00323.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
missense_variant | MODERATE | c.2293C>G | p.Pro765Ala | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 9/15 | 2394/5214 | 2293/3246 | 765/1081 | chr12 | 120216281 | ||
| chr12:120216493
|
G | A | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2081C>T | p.Thr694Ile | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 9/15 | 2182/5214 | 2081/3246 | 694/1081 | chr12 | 120216493 | ||
| chr12:120216902
|
T | C | 1 | a0005 | 3 | HG02257.hp2 HG02486.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.1931A>G | p.Glu644Gly | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 8/15 | 2032/5214 | 1931/3246 | 644/1081 | chr12 | 120216902 | ||
| chr12:120217109
|
G | T | 1 | a0011 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1724C>A | p.Ser575Tyr | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 8/15 | 1825/5214 | 1724/3246 | 575/1081 | chr12 | 120217109 | ||
| chr12:120217112
|
C | T | 1 | a0009 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1721G>A | p.Arg574Gln | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 8/15 | 1822/5214 | 1721/3246 | 574/1081 | chr12 | 120217112 | ||
| chr12:120219367
|
C | A | 1 | a0008 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.1556G>T | p.Arg519Met | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/15 | 1657/5214 | 1556/3246 | 519/1081 | chr12 | 120219367 | ||
| chr12:120219574
|
G | A | 1 | a0004 | 4 | HG02027.hp2 HG02074.hp2 NA18747.hp1 others(1): Show |
missense_variant | MODERATE | c.1349C>T | p.Pro450Leu | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/15 | 1450/5214 | 1349/3246 | 450/1081 | chr12 | 120219574 | ||
| chr12:120222977
|
C | T | 1 | a0012 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.379G>A | p.Ala127Thr | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 4/15 | 480/5214 | 379/3246 | 127/1081 | chr12 | 120222977 | ||
| chr12:120224167
|
C | T | 1 | a0006 | 2 | HG00438.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.224G>A | p.Arg75Gln | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 2/15 | 325/5214 | 224/3246 | 75/1081 | chr12 | 120224167 | ||
| chr12:120224174
|
T | C | 11 | a0001a0002a0004others(8): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
missense_variant | MODERATE | c.217A>G | p.Ser73Gly | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 2/15 | 318/5214 | 217/3246 | 73/1081 | chr12 | 120224174 | ||
| chr12:120224246
|
C | T | 1 | a0007 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.145G>A | p.Val49Ile | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 2/15 | 246/5214 | 145/3246 | 49/1081 | chr12 | 120224246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120212569
|
C | T | 1 | a0001c0010 | 2 | HG02970.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.2991G>A | p.Thr997Thr | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 3092/5214 | 2991/3246 | 997/1081 | chr12 | 120212569 | ||
| chr12:120213980
|
C | T | 1 | a0001c0024 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.2841G>A | p.Glu947Glu | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/15 | 2942/5214 | 2841/3246 | 947/1081 | chr12 | 120213980 | ||
| chr12:120214855
|
G | A | 3 | a0001c0005a0002c0011a0005c0008 | 10 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
synonymous_variant | LOW | c.2718C>T | p.Arg906Arg | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 12/15 | 2819/5214 | 2718/3246 | 906/1081 | chr12 | 120214855 | ||
| chr12:120215112
|
G | A | 1 | a0002c0012 | 2 | HG02886.hp2 HG02895.hp2 |
synonymous_variant | LOW | c.2565C>T | p.Ile855Ile | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 11/15 | 2666/5214 | 2565/3246 | 855/1081 | chr12 | 120215112 | ||
| chr12:120215157
|
G | A | 2 | a0002c0026a0008c0028 | 2 | HG01928.hp2 HG01978.hp2 |
synonymous_variant | LOW | c.2520C>T | p.Val840Val | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 11/15 | 2621/5214 | 2520/3246 | 840/1081 | chr12 | 120215157 | ||
| chr12:120215614
|
G | A | 1 | a0001c0025 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.2349C>T | p.Ala783Ala | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 10/15 | 2450/5214 | 2349/3246 | 783/1081 | chr12 | 120215614 | ||
| chr12:120216483
|
C | T | 1 | a0001c0023 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.2091G>A | p.Ala697Ala | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 9/15 | 2192/5214 | 2091/3246 | 697/1081 | chr12 | 120216483 | ||
| chr12:120216871
|
C | T | 1 | a0001c0022 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.1962G>A | p.Gly654Gly | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 8/15 | 2063/5214 | 1962/3246 | 654/1081 | chr12 | 120216871 | ||
| chr12:120216934
|
C | G | 1 | a0002c0019 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.1899G>C | p.Ala633Ala | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 8/15 | 2000/5214 | 1899/3246 | 633/1081 | chr12 | 120216934 | ||
| chr12:120219468
|
A | G | 5 | a0001c0005a0001c0030a0002c0019others(2): Show | 12 | HG00438.hp2 HG02257.hp2 HG02280.hp1 others(9): Show |
synonymous_variant | LOW | c.1455T>C | p.His485His | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/15 | 1556/5214 | 1455/3246 | 485/1081 | chr12 | 120219468 | ||
| chr12:120219741
|
G | C | 1 | a0001c0006 | 4 | HG02486.hp2 HG02559.hp1 HG03471.hp1 others(1): Show |
synonymous_variant | LOW | c.1182C>G | p.Leu394Leu | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/15 | 1283/5214 | 1182/3246 | 394/1081 | chr12 | 120219741 | ||
| chr12:120219975
|
G | T | 3 | a0001c0004a0001c0006a0001c0014 | 20 | HG01109.hp1 HG01943.hp1 HG02055.hp1 others(17): Show |
synonymous_variant | LOW | c.948C>A | p.Thr316Thr | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/15 | 1049/5214 | 948/3246 | 316/1081 | chr12 | 120219975 | ||
| chr12:120220038
|
C | T | 1 | a0001c0018 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.885G>A | p.Pro295Pro | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/15 | 986/5214 | 885/3246 | 295/1081 | chr12 | 120220038 | ||
| chr12:120221653
|
G | A | 1 | a0001c0017 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.801C>T | p.Asp267Asp | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/15 | 902/5214 | 801/3246 | 267/1081 | chr12 | 120221653 | ||
| chr12:120222909
|
C | T | 1 | a0001c0017 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.447G>A | p.Leu149Leu | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 4/15 | 548/5214 | 447/3246 | 149/1081 | chr12 | 120222909 | ||
| chr12:120222993
|
G | A | 1 | a0001c0029 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.363C>T | p.Pro121Pro | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 4/15 | 464/5214 | 363/3246 | 121/1081 | chr12 | 120222993 | ||
| chr12:120223822
|
T | A | 1 | a0001c0013 | 2 | HG02809.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.252A>T | p.Ser84Ser | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 3/15 | 353/5214 | 252/3246 | 84/1081 | chr12 | 120223822 | ||
| chr12:120224274
|
T | C | 1 | a0001c0030 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.117A>G | p.Thr39Thr | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 2/15 | 218/5214 | 117/3246 | 39/1081 | chr12 | 120224274 | ||
| chr12:120224364
|
C | T | 1 | a0001c0014 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.27G>A | p.Ala9Ala | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 2/15 | 128/5214 | 27/3246 | 9/1081 | chr12 | 120224364 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120210507
|
C | G | 2 | a0001c0030t0004a0006c0009t0004 | 3 | HG00438.hp2 HG03041.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1807G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 1807 | chr12 | 120210507 | |||||
| chr12:120210560
|
C | T | 2 | a0001c0030t0004a0006c0009t0004 | 3 | HG00438.hp2 HG03041.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1754G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 1754 | chr12 | 120210560 | |||||
| chr12:120210673
|
T | G | 1 | a0001c0001t0007 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 1641 | chr12 | 120210673 | |||||
| chr12:120210685
|
G | A | 1 | a0001c0001t0005 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1629C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 1629 | chr12 | 120210685 | |||||
| chr12:120211098
|
G | A | 1 | a0001c0022t0012 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1216C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 1216 | chr12 | 120211098 | |||||
| chr12:120211443
|
A | G | 1 | a0001c0001t0010 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*871T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 871 | chr12 | 120211443 | |||||
| chr12:120211488
|
C | T | 1 | a0001c0001t0006 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*826G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 826 | chr12 | 120211488 | |||||
| chr12:120211592
|
C | T | 1 | a0001c0001t0009 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 722 | chr12 | 120211592 | |||||
| chr12:120211777
|
G | A | 1 | a0001c0001t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*537C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 537 | chr12 | 120211777 | |||||
| chr12:120211847
|
C | A | 2 | a0001c0001t0003a0001c0010t0003 | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*467G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 467 | chr12 | 120211847 | |||||
| chr12:120211953
|
G | GC | 2 | a0001c0001t0003a0001c0010t0003 | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*360dupG | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 360 | chr12 | 120211953 | |||||
| chr12:120211975
|
A | C | 1 | a0001c0004t0008 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*339T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 339 | chr12 | 120211975 | |||||
| chr12:120212022
|
C | T | 1 | a0001c0001t0005 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 292 | chr12 | 120212022 | |||||
| chr12:120212086
|
G | A | 1 | a0001c0022t0012 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 228 | chr12 | 120212086 | |||||
| chr12:120212167
|
C | T | 8 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(5): Show | 99 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*147G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 15/15 | 147 | chr12 | 120212167 | |||||
| chr12:120265662
|
C | A | 1 | a0010c0027t0013 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/15 | 33 | chr12 | 120265662 | |||||
| chr12:120265686
|
C | A | 1 | a0001c0001t0014 | 1 | NA18949.hp1 | 5_prime_UTR_variant | MODIFIER | c.-57G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/15 | 57 | chr12 | 120265686 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:120212618
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0021others(17): Show | 26 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.2980-38G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120212618 | ||||||
| chr12:120212833
|
G | A | 2 | a0002c0002t0001g0090a0002c0002t0001g0091 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2980-253C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120212833 | ||||||
| chr12:120212845
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2980-265C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120212845 | ||||||
| chr12:120212992
|
G | A | 1 | a0001c0001t0002g0166 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2980-412C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120212992 | ||||||
| chr12:120212999
|
C | T | 1 | a0002c0002t0001g0159 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2980-419G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120212999 | ||||||
| chr12:120213208
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2980-628C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120213208 | ||||||
| chr12:120213367
|
G | A | 2 | a0001c0001t0003g0206a0001c0001t0003g0208 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2979+475C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120213367 | ||||||
| chr12:120213382
|
AAAAAG | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(64): Show | 86 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.2979+455_2979+459d others(7): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120213382 | ||||||
| chr12:120213419
|
C | T | 1 | a0001c0014t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2979+423G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120213419 | ||||||
| chr12:120213807
|
C | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2979+35G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 14/14 | chr12 | 120213807 | ||||||
| chr12:120214323
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0203 | 2 | NA18948.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.2749-106C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 12/14 | chr12 | 120214323 | ||||||
| chr12:120214656
|
C | G | 1 | a0001c0001t0002g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2748+169G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 12/14 | chr12 | 120214656 | ||||||
| chr12:120214717
|
C | T | 2 | a0001c0005t0001g0047a0001c0005t0001g0048 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2748+108G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 12/14 | chr12 | 120214717 | ||||||
| chr12:120214738
|
C | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2748+87G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 12/14 | chr12 | 120214738 | ||||||
| chr12:120214745
|
C | T | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2748+80G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 12/14 | chr12 | 120214745 | ||||||
| chr12:120214803
|
C | T | 1 | a0003c0003t0001g0115 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2748+22G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 12/14 | chr12 | 120214803 | ||||||
| chr12:120215008
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2575-10T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 11/14 | chr12 | 120215008 | ||||||
| chr12:120215054
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0257 | 2 | HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2574+49G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 11/14 | chr12 | 120215054 | ||||||
| chr12:120215095
|
C | T | 1 | a0001c0030t0004g0173 | 1 | HG03041.hp1 | splice_region_variant&intron_variant | LOW | c.2574+8G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 11/14 | chr12 | 120215095 | ||||||
| chr12:120215321
|
G | A | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2404-48C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 10/14 | chr12 | 120215321 | ||||||
| chr12:120215526
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2403+34G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 10/14 | chr12 | 120215526 | ||||||
| chr12:120215809
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2302-148A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 9/14 | chr12 | 120215809 | ||||||
| chr12:120215930
|
C | T | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2302-269G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 9/14 | chr12 | 120215930 | ||||||
| chr12:120216101
|
G | T | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2301+172C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 9/14 | chr12 | 120216101 | ||||||
| chr12:120216108
|
G | T | 1 | a0001c0001t0002g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2301+165C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 9/14 | chr12 | 120216108 | ||||||
| chr12:120216627
|
C | T | 10 | a0001c0001t0003g0204a0001c0001t0003g0206a0001c0001t0003g0207others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1993-46G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 8/14 | chr12 | 120216627 | ||||||
| chr12:120216785
|
C | T | 1 | a0001c0017t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1992+56G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 8/14 | chr12 | 120216785 | ||||||
| chr12:120217236
|
C | T | 1 | a0006c0009t0004g0035 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1717-120G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217236 | ||||||
| chr12:120217237
|
G | A | 1 | a0001c0004t0001g0052 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1717-121C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217237 | ||||||
| chr12:120217312
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1717-196G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217312 | ||||||
| chr12:120217592
|
TG | T | 12 | a0002c0002t0001g0019a0002c0002t0001g0090a0002c0002t0001g0155others(9): Show | 13 | HG02615.hp1 HG02615.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-477delC | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217592 | ||||||
| chr12:120217618
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1717-502G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217618 | ||||||
| chr12:120217643
|
G | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 123 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1717-527C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217643 | ||||||
| chr12:120217764
|
T | G | 3 | a0001c0001t0002g0123a0001c0004t0001g0042a0001c0004t0008g0040 | 3 | HG02523.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1717-648A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217764 | ||||||
| chr12:120217919
|
GT | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(60): Show | 82 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.1717-804delA | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120217919 | ||||||
| chr12:120218042
|
A | AT | 14 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(11): Show | 14 | HG00609.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1717-927dupA | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218042 | ||||||
| chr12:120218042
|
AT | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(67): Show | 88 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1717-927delA | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218042 | ||||||
| chr12:120218121
|
T | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0021others(17): Show | 26 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1717-1005A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218121 | ||||||
| chr12:120218361
|
G | T | 10 | a0001c0001t0003g0204a0001c0001t0003g0206a0001c0001t0003g0207others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1716+846C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218361 | ||||||
| chr12:120218404
|
A | G | 11 | a0001c0005t0001g0044a0001c0005t0001g0047a0001c0005t0001g0048others(8): Show | 11 | HG00438.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1716+803T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218404 | ||||||
| chr12:120218525
|
C | G | 1 | a0001c0001t0007g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1716+682G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218525 | ||||||
| chr12:120218795
|
C | T | 8 | a0001c0005t0001g0044a0001c0005t0001g0047a0001c0005t0001g0048others(5): Show | 8 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1716+412G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218795 | ||||||
| chr12:120218972
|
C | T | 1 | a0001c0029t0002g0122 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1716+235G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120218972 | ||||||
| chr12:120219018
|
G | A | 2 | a0001c0004t0001g0043a0001c0004t0001g0060 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1716+189C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120219018 | ||||||
| chr12:120219148
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1716+59G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 7/14 | chr12 | 120219148 | ||||||
| chr12:120220167
|
G | A | 1 | a0002c0002t0001g0216 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.832-76C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220167 | ||||||
| chr12:120220317
|
C | T | 1 | a0003c0003t0001g0109 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.832-226G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220317 | ||||||
| chr12:120220358
|
G | C | 2 | a0001c0004t0001g0042a0001c0004t0008g0040 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.832-267C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220358 | ||||||
| chr12:120220482
|
T | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.832-391A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220482 | ||||||
| chr12:120220555
|
T | C | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.832-464A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220555 | ||||||
| chr12:120220642
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.832-551G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220642 | ||||||
| chr12:120220773
|
G | A | 3 | a0001c0030t0004g0173a0006c0009t0004g0034a0006c0009t0004g0035 | 3 | HG00438.hp2 HG03041.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.832-682C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220773 | ||||||
| chr12:120220925
|
G | A | 1 | a0001c0030t0004g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.831+698C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220925 | ||||||
| chr12:120220980
|
A | G | 1 | a0001c0030t0004g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.831+643T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120220980 | ||||||
| chr12:120221045
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.831+578G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120221045 | ||||||
| chr12:120221276
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.831+347G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120221276 | ||||||
| chr12:120221366
|
G | A | 2 | a0001c0001t0001g0046a0009c0020t0001g0045 | 2 | HG01891.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.831+257C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 6/14 | chr12 | 120221366 | ||||||
| chr12:120221766
|
G | A | 1 | a0001c0001t0002g0152 | 1 | NA19057.hp1 | splice_region_variant&intron_variant | LOW | c.696-8C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120221766 | ||||||
| chr12:120221793
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.696-35G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120221793 | ||||||
| chr12:120221846
|
G | C | 1 | a0001c0017t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.696-88C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120221846 | ||||||
| chr12:120221970
|
C | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0138 | 3 | HG00544.hp2 HG00621.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.696-212G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120221970 | ||||||
| chr12:120222055
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.696-297G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120222055 | ||||||
| chr12:120222152
|
T | A | 1 | a0006c0009t0004g0035 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.696-394A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120222152 | ||||||
| chr12:120222194
|
C | T | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(224): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.695+355G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120222194 | ||||||
| chr12:120222303
|
A | T | 10 | a0001c0001t0003g0204a0001c0001t0003g0206a0001c0001t0003g0207others(7): Show | 10 | HG01243.hp1 HG02055.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.695+246T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 5/14 | chr12 | 120222303 | ||||||
| chr12:120223209
|
T | C | 3 | a0001c0030t0004g0173a0006c0009t0004g0034a0006c0009t0004g0035 | 3 | HG00438.hp2 HG03041.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.357-210A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 3/14 | chr12 | 120223209 | ||||||
| chr12:120223214
|
C | T | 1 | a0002c0002t0001g0172 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.357-215G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 3/14 | chr12 | 120223214 | ||||||
| chr12:120223294
|
C | T | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.357-295G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 3/14 | chr12 | 120223294 | ||||||
| chr12:120223304
|
G | A | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.357-305C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 3/14 | chr12 | 120223304 | ||||||
| chr12:120223641
|
C | T | 14 | a0001c0004t0001g0043a0001c0004t0001g0051a0001c0004t0001g0052others(11): Show | 14 | HG01109.hp1 HG01943.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.356+77G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 3/14 | chr12 | 120223641 | ||||||
| chr12:120223865
|
C | G | 3 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0023t0001g0221 | 3 | HG02451.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.241-32G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 2/14 | chr12 | 120223865 | ||||||
| chr12:120224394
|
C | G | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-17G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120224394 | ||||||
| chr12:120224432
|
C | T | 3 | a0001c0001t0002g0136a0002c0002t0001g0089a0002c0002t0001g0092 | 3 | HG00323.hp1 HG01981.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.14-55G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120224432 | ||||||
| chr12:120224529
|
C | A | 2 | a0001c0013t0001g0213a0001c0013t0001g0215 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.14-152G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120224529 | ||||||
| chr12:120224662
|
G | A | 1 | a0001c0030t0004g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.14-285C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120224662 | ||||||
| chr12:120224702
|
T | C | 20 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0021others(17): Show | 26 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.14-325A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120224702 | ||||||
| chr12:120224791
|
A | G | 12 | a0001c0005t0001g0044a0001c0005t0001g0047a0001c0005t0001g0048others(9): Show | 12 | HG00438.hp2 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.14-414T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120224791 | ||||||
| chr12:120224840
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.14-463C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120224840 | ||||||
| chr12:120225036
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0155a0002c0002t0001g0156others(6): Show | 10 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-659C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225036 | ||||||
| chr12:120225055
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.14-678G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225055 | ||||||
| chr12:120225069
|
C | G | 1 | a0002c0002t0001g0078 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.14-692G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225069 | ||||||
| chr12:120225123
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.14-746A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225123 | ||||||
| chr12:120225203
|
A | AT | 9 | a0001c0005t0001g0044a0001c0005t0001g0047a0001c0005t0001g0048others(6): Show | 9 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.14-827dupA | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225203 | ||||||
| chr12:120225245
|
A | G | 12 | a0001c0005t0001g0044a0001c0005t0001g0047a0001c0005t0001g0048others(9): Show | 12 | HG00438.hp2 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.14-868T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225245 | ||||||
| chr12:120225350
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0125 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.14-973C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225350 | ||||||
| chr12:120225429
|
G | A | 2 | a0001c0001t0001g0220a0001c0001t0001g0222 | 2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.14-1052C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225429 | ||||||
| chr12:120225464
|
A | G | 1 | a0001c0001t0006g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.14-1087T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225464 | ||||||
| chr12:120225485
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 163 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.14-1108C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225485 | ||||||
| chr12:120225958
|
G | A | 3 | a0001c0001t0002g0013a0001c0001t0002g0066a0001c0001t0002g0177 | 4 | HG02109.hp1 HG02280.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-1581C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120225958 | ||||||
| chr12:120226009
|
C | T | 9 | a0002c0002t0001g0019a0002c0002t0001g0155a0002c0002t0001g0156others(6): Show | 10 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-1632G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120226009 | ||||||
| chr12:120226190
|
T | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0198 | 3 | NA18945.hp2 NA18971.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.14-1813A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120226190 | ||||||
| chr12:120226205
|
A | G | 1 | a0006c0009t0004g0035 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.14-1828T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120226205 | ||||||
| chr12:120226468
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0199 | 3 | NA18944.hp1 NA18950.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.14-2091T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120226468 | ||||||
| chr12:120227893
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.14-3516C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120227893 | ||||||
| chr12:120228361
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.14-3984G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120228361 | ||||||
| chr12:120228577
|
T | A | 1 | a0001c0023t0001g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.14-4200A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120228577 | ||||||
| chr12:120228583
|
G | A | 1 | a0001c0023t0001g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.14-4206C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120228583 | ||||||
| chr12:120228662
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(20): Show | 33 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.14-4285C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120228662 | ||||||
| chr12:120228683
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.14-4306C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120228683 | ||||||
| chr12:120228892
|
G | C | 1 | a0001c0001t0002g0164 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.14-4515C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120228892 | ||||||
| chr12:120228971
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.14-4594C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120228971 | ||||||
| chr12:120229070
|
G | A | 1 | a0001c0001t0002g0134 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.14-4693C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120229070 | ||||||
| chr12:120229142
|
C | T | 20 | a0001c0004t0001g0042a0001c0004t0001g0043a0001c0004t0001g0051others(17): Show | 20 | HG01109.hp1 HG01943.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.14-4765G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120229142 | ||||||
| chr12:120229296
|
G | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(263): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.14-4919C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120229296 | ||||||
| chr12:120229391
|
A | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(86): Show | 114 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.14-5014T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120229391 | ||||||
| chr12:120229409
|
G | C | 20 | a0001c0004t0001g0042a0001c0004t0001g0043a0001c0004t0001g0051others(17): Show | 20 | HG01109.hp1 HG01943.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.14-5032C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120229409 | ||||||
| chr12:120229977
|
C | T | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-5600G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120229977 | ||||||
| chr12:120230011
|
G | A | 1 | a0002c0002t0001g0236 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.14-5634C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230011 | ||||||
| chr12:120230015
|
TGCATTCT others(36): Show |
T | 1 | a0001c0001t0002g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.14-5681_14-5639del others(43): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230015 | ||||||
| chr12:120230130
|
G | T | 1 | a0002c0002t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.14-5753C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230130 | ||||||
| chr12:120230139
|
A | G | 2 | a0001c0001t0002g0093a0001c0001t0002g0180 | 2 | HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.14-5762T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230139 | ||||||
| chr12:120230183
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 150 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.14-5806T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230183 | ||||||
| chr12:120230218
|
C | T | 2 | a0001c0001t0010g0083a0001c0024t0001g0082 | 2 | HG02738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.14-5841G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230218 | ||||||
| chr12:120230332
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.14-5955C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230332 | ||||||
| chr12:120230493
|
G | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0226a0001c0001t0001g0227 | 6 | NA18939.hp2 NA18957.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-6116C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230493 | ||||||
| chr12:120230610
|
G | A | 5 | a0003c0003t0001g0072a0003c0003t0001g0098a0003c0003t0001g0106others(2): Show | 5 | HG01346.hp1 HG01928.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-6233C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230610 | ||||||
| chr12:120230706
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.14-6329C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230706 | ||||||
| chr12:120230731
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.14-6354C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230731 | ||||||
| chr12:120230796
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0271 | 2 | NA18978.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.14-6419G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230796 | ||||||
| chr12:120230868
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.14-6491G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230868 | ||||||
| chr12:120230909
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.14-6532C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120230909 | ||||||
| chr12:120231107
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.14-6730A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120231107 | ||||||
| chr12:120231367
|
A | T | 3 | a0001c0001t0001g0046a0001c0022t0012g0153a0009c0020t0001g0045 | 3 | HG01891.hp2 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.14-6990T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120231367 | ||||||
| chr12:120231435
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0249a0001c0001t0009g0260 | 3 | HG02027.hp1 HG02135.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.14-7058C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120231435 | ||||||
| chr12:120231557
|
C | T | 1 | a0001c0013t0001g0215 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.14-7180G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120231557 | ||||||
| chr12:120231574
|
G | A | 1 | a0001c0017t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.14-7197C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120231574 | ||||||
| chr12:120232146
|
C | G | 1 | a0001c0030t0004g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.14-7769G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120232146 | ||||||
| chr12:120232229
|
C | T | 21 | a0001c0004t0001g0042a0001c0004t0001g0043a0001c0004t0001g0051others(18): Show | 21 | HG01109.hp1 HG01943.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.14-7852G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120232229 | ||||||
| chr12:120232484
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.14-8107G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120232484 | ||||||
| chr12:120232576
|
A | C | 21 | a0001c0001t0001g0046a0001c0001t0010g0083a0001c0024t0001g0082others(18): Show | 22 | HG00323.hp1 HG00738.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.14-8199T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120232576 | ||||||
| chr12:120232911
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.14-8534G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120232911 | ||||||
| chr12:120233050
|
C | T | 4 | a0001c0001t0001g0233a0001c0001t0001g0252a0001c0001t0001g0275others(1): Show | 4 | HG02040.hp2 HG02056.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-8673G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233050 | ||||||
| chr12:120233163
|
C | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(95): Show | 124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.14-8786G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233163 | ||||||
| chr12:120233224
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.14-8847G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233224 | ||||||
| chr12:120233242
|
C | T | 1 | a0001c0014t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.14-8865G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233242 | ||||||
| chr12:120233276
|
C | T | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.14-8899G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233276 | ||||||
| chr12:120233329
|
T | G | 1 | a0001c0025t0001g0244 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.14-8952A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233329 | ||||||
| chr12:120233339
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.14-8962G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233339 | ||||||
| chr12:120233526
|
G | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 27 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.14-9149C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233526 | ||||||
| chr12:120233531
|
C | T | 1 | a0001c0004t0001g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.14-9154G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233531 | ||||||
| chr12:120233601
|
C | T | 6 | a0001c0005t0001g0044a0001c0005t0001g0047a0001c0005t0001g0048others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-9224G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233601 | ||||||
| chr12:120233729
|
T | C | 2 | a0002c0002t0001g0090a0002c0002t0001g0091 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.14-9352A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233729 | ||||||
| chr12:120233774
|
C | T | 7 | a0002c0002t0001g0074a0002c0002t0001g0075a0002c0002t0001g0076others(4): Show | 7 | HG02717.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.14-9397G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233774 | ||||||
| chr12:120233820
|
A | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 132 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.14-9443T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233820 | ||||||
| chr12:120233844
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.14-9467G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233844 | ||||||
| chr12:120233891
|
A | G | 20 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0021others(17): Show | 26 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.14-9514T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233891 | ||||||
| chr12:120233892
|
T | C | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.14-9515A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120233892 | ||||||
| chr12:120234104
|
AAG | A | 95 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0010others(92): Show | 109 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.14-9729_14-9728del others(2): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120234104 | ||||||
| chr12:120234544
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(102): Show | 131 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.14-10167G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120234544 | ||||||
| chr12:120234717
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0246a0001c0001t0001g0271 | 3 | NA18953.hp2 NA18978.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.14-10340C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120234717 | ||||||
| chr12:120234726
|
G | C | 3 | a0001c0006t0001g0038a0001c0006t0001g0039a0001c0006t0001g0169 | 3 | HG02486.hp2 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.14-10349C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120234726 | ||||||
| chr12:120234745
|
T | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 27 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.14-10368A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120234745 | ||||||
| chr12:120234811
|
C | T | 1 | a0006c0009t0004g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.14-10434G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120234811 | ||||||
| chr12:120234840
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.14-10463T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120234840 | ||||||
| chr12:120235040
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0267 | 2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.14-10663G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120235040 | ||||||
| chr12:120235330
|
A | G | 3 | a0002c0002t0001g0084a0002c0002t0001g0086a0011c0021t0001g0085 | 3 | HG00738.hp1 HG01071.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.14-10953T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120235330 | ||||||
| chr12:120235335
|
G | C | 1 | a0001c0001t0002g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.14-10958C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120235335 | ||||||
| chr12:120235653
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0248a0001c0001t0001g0250 | 3 | NA18747.hp2 NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.14-11276G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120235653 | ||||||
| chr12:120235928
|
T | C | 1 | a0001c0001t0001g0219 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.14-11551A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120235928 | ||||||
| chr12:120236040
|
G | A | 1 | a0001c0004t0001g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.14-11663C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236040 | ||||||
| chr12:120236235
|
C | T | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.14-11858G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236235 | ||||||
| chr12:120236404
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.14-12027G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236404 | ||||||
| chr12:120236476
|
C | CT | 8 | a0001c0001t0001g0046a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00642.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-12100dupA | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236476 | ||||||
| chr12:120236476
|
CT | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 112 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.14-12100delA | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236476 | ||||||
| chr12:120236516
|
C | T | 1 | a0003c0003t0001g0100 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.14-12139G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236516 | ||||||
| chr12:120236545
|
T | G | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.14-12168A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236545 | ||||||
| chr12:120236602
|
G | A | 2 | a0001c0001t0002g0119a0001c0018t0002g0142 | 2 | NA18952.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.14-12225C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236602 | ||||||
| chr12:120236633
|
C | T | 1 | a0001c0004t0001g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.14-12256G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236633 | ||||||
| chr12:120236735
|
A | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0021others(18): Show | 27 | HG00408.hp2 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.14-12358T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236735 | ||||||
| chr12:120236768
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.14-12391G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236768 | ||||||
| chr12:120236858
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.14-12481C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120236858 | ||||||
| chr12:120237126
|
C | CGT | 23 | a0001c0001t0001g0046a0001c0001t0001g0064a0001c0001t0001g0065others(20): Show | 23 | HG00140.hp1 HG00735.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.14-12751_14-12750d others(4): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237126 | ||||||
| chr12:120237126
|
CGTGT | C | 4 | a0001c0001t0002g0017a0001c0001t0002g0128a0001c0001t0002g0131others(1): Show | 5 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-12753_14-12750d others(6): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237126 | ||||||
| chr12:120237147
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 138 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.14-12770T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237147 | ||||||
| chr12:120237148
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.14-12771A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237148
|
T | TAC | 9 | a0001c0001t0002g0013a0001c0001t0002g0053a0001c0001t0002g0066others(6): Show | 12 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.14-12773_14-12772d others(4): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237148
|
TAC | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 100 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.14-12773_14-12772d others(4): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237148
|
TACAC | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0002g0130others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-12775_14-12772d others(6): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237148
|
TACACAC | T | 4 | a0001c0001t0001g0196a0001c0001t0002g0014a0001c0001t0002g0125others(1): Show | 5 | HG01884.hp1 HG03017.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.14-12777_14-12772d others(8): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237148
|
TACACACA others(1): Show |
T | 25 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0190others(22): Show | 30 | HG01168.hp1 HG01169.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.14-12779_14-12772d others(10): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237148
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.14-12781_14-12772d others(12): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237148
|
TACACACA others(7): Show |
T | 8 | a0001c0001t0001g0007a0001c0001t0001g0022a0001c0001t0001g0023others(5): Show | 12 | HG00408.hp2 NA18944.hp1 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.14-12785_14-12772d others(16): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237148 | ||||||
| chr12:120237149
|
A | G | 4 | a0001c0001t0001g0223a0001c0001t0001g0246a0001c0001t0001g0271others(1): Show | 4 | HG02717.hp1 NA18953.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-12772T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237149 | ||||||
| chr12:120237150
|
C | T | 24 | a0001c0001t0001g0129a0001c0001t0001g0223a0001c0001t0001g0246others(21): Show | 24 | HG00408.hp1 HG01109.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.14-12773G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237150 | ||||||
| chr12:120237152
|
C | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(80): Show | 99 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.14-12775G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237152 | ||||||
| chr12:120237155
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0002g0125 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.14-12778T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237155 | ||||||
| chr12:120237156
|
C | T | 3 | a0001c0001t0001g0196a0001c0001t0002g0014a0001c0001t0002g0125 | 4 | HG03017.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-12779G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237156 | ||||||
| chr12:120237158
|
C | T | 14 | a0001c0001t0002g0012a0001c0001t0002g0014a0001c0001t0002g0020others(11): Show | 17 | HG01433.hp2 HG02165.hp1 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.14-12781G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237158 | ||||||
| chr12:120237160
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.14-12783G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237160 | ||||||
| chr12:120237214
|
A | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 88 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.14-12837T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237214 | ||||||
| chr12:120237646
|
G | A | 11 | a0001c0001t0001g0205a0001c0001t0003g0204a0001c0001t0003g0206others(8): Show | 11 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.14-13269C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237646 | ||||||
| chr12:120237655
|
G | A | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.14-13278C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237655 | ||||||
| chr12:120237681
|
C | A | 4 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(1): Show | 4 | NA18962.hp2 NA18966.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-13304G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237681 | ||||||
| chr12:120237846
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.14-13469G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237846 | ||||||
| chr12:120237885
|
C | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0251 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14-13508G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237885 | ||||||
| chr12:120237954
|
C | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0180 | 2 | HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.14-13577G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120237954 | ||||||
| chr12:120238061
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.14-13684C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120238061 | ||||||
| chr12:120238287
|
G | A | 62 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0010others(59): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.14-13910C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120238287 | ||||||
| chr12:120238325
|
A | C | 3 | a0001c0001t0001g0241a0001c0001t0001g0248a0001c0001t0001g0250 | 3 | NA18747.hp2 NA18998.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.14-13948T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120238325 | ||||||
| chr12:120238377
|
C | T | 1 | a0001c0006t0001g0038 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.14-14000G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120238377 | ||||||
| chr12:120238436
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.14-14059C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120238436 | ||||||
| chr12:120238635
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0002g0096 | 2 | HG00639.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.14-14258G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120238635 | ||||||
| chr12:120238881
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.14-14504C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120238881 | ||||||
| chr12:120239190
|
T | C | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-14813A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120239190 | ||||||
| chr12:120239474
|
C | T | 59 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(56): Show | 64 | HG00408.hp2 HG01099.hp1 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.14-15097G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120239474 | ||||||
| chr12:120239497
|
G | A | 2 | a0001c0001t0001g0171a0001c0001t0002g0170 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.14-15120C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120239497 | ||||||
| chr12:120239577
|
G | A | 58 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(55): Show | 63 | HG00408.hp2 HG01099.hp1 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.14-15200C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120239577 | ||||||
| chr12:120239608
|
G | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 35 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-15231C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120239608 | ||||||
| chr12:120239784
|
A | T | 26 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0073others(23): Show | 29 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.14-15407T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120239784 | ||||||
| chr12:120239927
|
C | CT | 7 | a0001c0001t0001g0261a0001c0001t0002g0017a0001c0001t0002g0128others(4): Show | 8 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-15551dupA | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120239927 | ||||||
| chr12:120240054
|
C | G | 1 | a0001c0001t0002g0105 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.14-15677G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240054 | ||||||
| chr12:120240075
|
C | T | 2 | a0002c0002t0001g0156a0002c0002t0001g0158 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.14-15698G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240075 | ||||||
| chr12:120240129
|
T | A | 2 | a0001c0030t0004g0173a0002c0002t0001g0172 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.14-15752A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240129 | ||||||
| chr12:120240379
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-16002C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240379 | ||||||
| chr12:120240578
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(139): Show | 167 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.14-16201T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240578 | ||||||
| chr12:120240604
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.14-16227C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240604 | ||||||
| chr12:120240682
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0023t0001g0221 | 3 | HG02451.hp1 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.14-16305C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240682 | ||||||
| chr12:120240858
|
C | G | 1 | a0011c0021t0001g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.14-16481G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240858 | ||||||
| chr12:120240927
|
A | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 165 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.14-16550T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120240927 | ||||||
| chr12:120241043
|
G | C | 3 | a0001c0001t0001g0011a0002c0002t0001g0090a0002c0002t0001g0091 | 4 | HG01168.hp1 HG01169.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-16666C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120241043 | ||||||
| chr12:120241123
|
A | C | 28 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(25): Show | 33 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.14-16746T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120241123 | ||||||
| chr12:120241576
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.14-17199C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120241576 | ||||||
| chr12:120241826
|
G | A | 9 | a0002c0002t0001g0019a0002c0002t0001g0155a0002c0002t0001g0156others(6): Show | 10 | HG02615.hp1 HG02818.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-17449C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120241826 | ||||||
| chr12:120241996
|
T | C | 2 | a0001c0030t0004g0173a0002c0002t0001g0172 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.14-17619A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120241996 | ||||||
| chr12:120242077
|
C | T | 3 | a0001c0001t0002g0177a0001c0006t0001g0169a0002c0002t0001g0168 | 3 | HG02280.hp2 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.14-17700G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242077 | ||||||
| chr12:120242110
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.14-17733C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242110 | ||||||
| chr12:120242123
|
T | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 170 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.14-17746A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242123 | ||||||
| chr12:120242133
|
G | A | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.14-17756C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242133 | ||||||
| chr12:120242225
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.14-17848C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242225 | ||||||
| chr12:120242392
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.14-18015C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242392 | ||||||
| chr12:120242623
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.14-18246A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242623 | ||||||
| chr12:120242657
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-18280C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242657 | ||||||
| chr12:120242682
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(75): Show | 98 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.14-18305G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242682 | ||||||
| chr12:120242881
|
TA | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(59): Show | 67 | HG00323.hp2 HG00408.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.14-18505delT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242881 | ||||||
| chr12:120242946
|
C | G | 1 | a0001c0004t0001g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.14-18569G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242946 | ||||||
| chr12:120242951
|
A | G | 1 | a0002c0002t0001g0157 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.14-18574T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120242951 | ||||||
| chr12:120243005
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.14-18628C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243005 | ||||||
| chr12:120243009
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-18632C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243009 | ||||||
| chr12:120243115
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.14-18738G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243115 | ||||||
| chr12:120243116
|
G | A | 1 | a0001c0014t0001g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.14-18739C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243116 | ||||||
| chr12:120243313
|
T | G | 1 | a0001c0001t0002g0149 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.14-18936A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243313 | ||||||
| chr12:120243358
|
G | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.14-18981C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243358 | ||||||
| chr12:120243409
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.14-19032C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243409 | ||||||
| chr12:120243411
|
C | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 164 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.14-19034G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243411 | ||||||
| chr12:120243560
|
C | T | 6 | a0001c0001t0002g0069a0001c0005t0001g0044a0001c0005t0001g0047others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-19183G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243560 | ||||||
| chr12:120243654
|
C | A | 1 | a0001c0001t0002g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.14-19277G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243654 | ||||||
| chr12:120243697
|
C | T | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.14-19320G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243697 | ||||||
| chr12:120243712
|
G | A | 3 | a0001c0005t0001g0044a0001c0005t0001g0049a0001c0005t0001g0050 | 3 | HG02280.hp1 HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.14-19335C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243712 | ||||||
| chr12:120243829
|
A | C | 1 | a0001c0001t0002g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.14-19452T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243829 | ||||||
| chr12:120243919
|
T | C | 2 | a0001c0005t0001g0047a0001c0005t0001g0048 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.14-19542A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120243919 | ||||||
| chr12:120244097
|
G | T | 28 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(25): Show | 33 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.14-19720C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244097 | ||||||
| chr12:120244398
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.14-20021C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244398 | ||||||
| chr12:120244418
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.14-20041C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244418 | ||||||
| chr12:120244421
|
C | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.14-20044G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244421 | ||||||
| chr12:120244428
|
C | T | 3 | a0001c0001t0002g0016a0001c0001t0002g0097a0001c0001t0002g0184 | 4 | HG00099.hp2 HG01943.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-20051G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244428 | ||||||
| chr12:120244462
|
C | G | 1 | a0003c0003t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.14-20085G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244462 | ||||||
| chr12:120244521
|
G | A | 10 | a0001c0001t0001g0205a0001c0001t0003g0204a0001c0001t0003g0206others(7): Show | 10 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.14-20144C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244521 | ||||||
| chr12:120244605
|
A | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 165 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.14-20228T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244605 | ||||||
| chr12:120244649
|
G | GA | 9 | a0001c0001t0001g0224a0001c0001t0001g0238a0001c0001t0001g0246others(6): Show | 9 | HG00544.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.14-20273dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244649 | ||||||
| chr12:120244666
|
T | A | 1 | a0001c0017t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.14-20289A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244666 | ||||||
| chr12:120244697
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.14-20320G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244697 | ||||||
| chr12:120244778
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.14-20401G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244778 | ||||||
| chr12:120244809
|
G | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0033a0001c0001t0002g0121others(2): Show | 7 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.14-20432C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244809 | ||||||
| chr12:120244846
|
A | G | 1 | a0003c0003t0001g0101 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.14-20469T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244846 | ||||||
| chr12:120244909
|
G | C | 1 | a0001c0004t0001g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.14-20532C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244909 | ||||||
| chr12:120244928
|
T | C | 1 | a0003c0003t0001g0111 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.14-20551A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244928 | ||||||
| chr12:120244985
|
G | A | 10 | a0001c0001t0001g0205a0001c0001t0003g0204a0001c0001t0003g0206others(7): Show | 10 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.14-20608C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120244985 | ||||||
| chr12:120245156
|
G | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.13+20461C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245156 | ||||||
| chr12:120245207
|
G | C | 1 | a0001c0029t0002g0122 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.13+20410C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245207 | ||||||
| chr12:120245223
|
C | T | 1 | a0001c0017t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.13+20394G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245223 | ||||||
| chr12:120245431
|
G | T | 1 | a0001c0001t0011g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.13+20186C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245431 | ||||||
| chr12:120245441
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.13+20176T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245441 | ||||||
| chr12:120245490
|
C | CA | 18 | a0001c0001t0002g0053a0001c0001t0002g0066a0001c0001t0003g0281others(15): Show | 18 | HG01109.hp1 HG01943.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.13+20126dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245490 | ||||||
| chr12:120245584
|
A | G | 1 | a0001c0005t0001g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.13+20033T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245584 | ||||||
| chr12:120245704
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0009g0260 | 2 | HG02027.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.13+19913G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245704 | ||||||
| chr12:120245712
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.13+19905G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245712 | ||||||
| chr12:120245779
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.13+19838G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245779 | ||||||
| chr12:120245787
|
C | CA | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG00544.hp1 HG01891.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+19829dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245787 | ||||||
| chr12:120245787
|
CA | C | 19 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0267others(16): Show | 19 | HG00323.hp2 HG01070.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.13+19829delT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245787 | ||||||
| chr12:120245824
|
A | G | 1 | a0001c0004t0001g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.13+19793T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245824 | ||||||
| chr12:120245853
|
T | C | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.13+19764A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245853 | ||||||
| chr12:120245860
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.13+19757G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120245860 | ||||||
| chr12:120246105
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.13+19512C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246105 | ||||||
| chr12:120246165
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.13+19452A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246165 | ||||||
| chr12:120246189
|
C | T | 1 | a0001c0006t0001g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.13+19428G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246189 | ||||||
| chr12:120246264
|
T | C | 2 | a0001c0005t0001g0047a0001c0005t0001g0048 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.13+19353A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246264 | ||||||
| chr12:120246514
|
C | CA | 9 | a0001c0001t0002g0105a0001c0001t0002g0123a0001c0001t0002g0183others(6): Show | 9 | HG01884.hp2 HG02280.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+19102dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246514 | ||||||
| chr12:120246514
|
CA | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 96 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.13+19102delT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246514 | ||||||
| chr12:120246529
|
A | G | 1 | a0001c0005t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.13+19088T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246529 | ||||||
| chr12:120246530
|
A | G | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+19087T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246530 | ||||||
| chr12:120246541
|
G | T | 1 | a0002c0002t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.13+19076C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246541 | ||||||
| chr12:120246589
|
T | C | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+19028A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246589 | ||||||
| chr12:120246725
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.13+18892G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246725 | ||||||
| chr12:120246942
|
C | A | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+18675G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120246942 | ||||||
| chr12:120247041
|
T | A | 1 | a0001c0001t0001g0248 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.13+18576A>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247041 | ||||||
| chr12:120247067
|
AAAG | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 66 | HG00408.hp2 HG01099.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.13+18547_13+18549d others(5): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247067 | ||||||
| chr12:120247463
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.13+18154G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247463 | ||||||
| chr12:120247517
|
C | T | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.13+18100G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247517 | ||||||
| chr12:120247646
|
G | A | 3 | a0001c0001t0001g0011a0002c0002t0001g0090a0002c0002t0001g0091 | 4 | HG01168.hp1 HG01169.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+17971C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247646 | ||||||
| chr12:120247655
|
G | T | 1 | a0001c0001t0002g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.13+17962C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247655 | ||||||
| chr12:120247690
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0010g0083others(11): Show | 16 | HG00099.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.13+17927G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247690 | ||||||
| chr12:120247710
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.13+17907C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247710 | ||||||
| chr12:120247734
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.13+17883C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247734 | ||||||
| chr12:120247944
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 164 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.13+17673A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120247944 | ||||||
| chr12:120248013
|
A | G | 1 | a0001c0004t0001g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.13+17604T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248013 | ||||||
| chr12:120248081
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.13+17536G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248081 | ||||||
| chr12:120248174
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.13+17443G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248174 | ||||||
| chr12:120248239
|
G | A | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.13+17378C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248239 | ||||||
| chr12:120248457
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.13+17160G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248457 | ||||||
| chr12:120248492
|
T | TCA | 37 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0032others(34): Show | 40 | HG00408.hp2 HG00597.hp1 HG01255.hp1 others(37): Show |
intron_variant | MODIFIER | c.13+17123_13+17124d others(4): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
T | TCACA | 22 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0046others(19): Show | 24 | HG00140.hp1 HG01109.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.13+17121_13+17124d others(6): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
T | TCACACA | 6 | a0001c0001t0003g0204a0001c0001t0003g0209a0001c0001t0003g0280others(3): Show | 6 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+17119_13+17124d others(8): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
T | TCACACAC others(1): Show |
7 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0201others(4): Show | 8 | HG02257.hp1 HG02622.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.13+17117_13+17124d others(10): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
T | TCACACAC others(3): Show |
1 | a0001c0001t0003g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.13+17115_13+17124d others(12): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
T | TCACACAC others(5): Show |
3 | a0001c0001t0001g0205a0001c0010t0003g0211a0001c0010t0003g0212 | 3 | HG01099.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.13+17113_13+17124d others(14): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
TCA | T | 43 | a0001c0001t0001g0064a0001c0001t0001g0129a0001c0001t0001g0195others(40): Show | 48 | HG00408.hp1 HG00673.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.13+17123_13+17124d others(4): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
TCACA | T | 41 | a0001c0001t0001g0011a0001c0001t0001g0024a0001c0001t0001g0218others(38): Show | 45 | HG00597.hp2 HG00639.hp1 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.13+17121_13+17124d others(6): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
TCACACA | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(37): Show | 58 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.13+17119_13+17124d others(8): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
TCACACAC others(1): Show |
T | 7 | a0001c0001t0001g0073a0001c0001t0001g0226a0001c0001t0001g0238others(4): Show | 7 | HG00323.hp1 HG01243.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+17117_13+17124d others(10): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248492
|
TCACACAC others(3): Show |
T | 12 | a0001c0001t0001g0269a0001c0001t0001g0279a0002c0002t0001g0025others(9): Show | 13 | HG00438.hp2 HG00544.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.13+17115_13+17124d others(12): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248492 | ||||||
| chr12:120248580
|
G | A | 1 | a0001c0004t0008g0040 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.13+17037C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248580 | ||||||
| chr12:120248648
|
G | A | 1 | a0001c0005t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.13+16969C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248648 | ||||||
| chr12:120248700
|
C | T | 1 | a0001c0022t0012g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.13+16917G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248700 | ||||||
| chr12:120248735
|
G | T | 7 | a0002c0002t0001g0074a0002c0002t0001g0075a0002c0002t0001g0076others(4): Show | 7 | HG02717.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+16882C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248735 | ||||||
| chr12:120248797
|
G | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.13+16820C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120248797 | ||||||
| chr12:120249154
|
A | G | 1 | a0001c0006t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13+16463T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249154 | ||||||
| chr12:120249266
|
C | CA | 12 | a0001c0001t0003g0281a0001c0004t0001g0043a0001c0004t0001g0055others(9): Show | 12 | HG01109.hp1 HG01943.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.13+16350dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249266 | ||||||
| chr12:120249277
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 163 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.13+16340C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249277 | ||||||
| chr12:120249400
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.13+16217T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249400 | ||||||
| chr12:120249625
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.13+15992G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249625 | ||||||
| chr12:120249740
|
C | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.13+15877G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249740 | ||||||
| chr12:120249757
|
C | T | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.13+15860G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249757 | ||||||
| chr12:120249895
|
T | C | 2 | a0001c0001t0002g0013a0001c0022t0012g0153 | 3 | HG02109.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.13+15722A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249895 | ||||||
| chr12:120249989
|
G | A | 10 | a0001c0001t0001g0205a0001c0001t0003g0204a0001c0001t0003g0206others(7): Show | 10 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.13+15628C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249989 | ||||||
| chr12:120249999
|
GCTGCCAA others(16): Show |
G | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+15595_13+15617d others(25): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120249999 | ||||||
| chr12:120250132
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 95 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.13+15485C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250132 | ||||||
| chr12:120250258
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.13+15359C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250258 | ||||||
| chr12:120250322
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.13+15295A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250322 | ||||||
| chr12:120250610
|
C | T | 1 | a0003c0003t0001g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.13+15007G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250610 | ||||||
| chr12:120250741
|
C | T | 1 | a0001c0010t0003g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+14876G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250741 | ||||||
| chr12:120250856
|
G | GTCC | 28 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(25): Show | 33 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.13+14760_13+14761i others(5): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250856 | ||||||
| chr12:120250857
|
C | A | 28 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(25): Show | 33 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.13+14760G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250857 | ||||||
| chr12:120250857
|
C | CCCA | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 133 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.13+14757_13+14759d others(5): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250857 | ||||||
| chr12:120250889
|
A | G | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.13+14728T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250889 | ||||||
| chr12:120250941
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.13+14676G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250941 | ||||||
| chr12:120250969
|
C | T | 2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.13+14648G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120250969 | ||||||
| chr12:120251001
|
C | T | 11 | a0001c0001t0001g0081a0001c0001t0010g0083a0001c0024t0001g0082others(8): Show | 12 | HG00099.hp1 HG02717.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.13+14616G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251001 | ||||||
| chr12:120251128
|
C | A | 3 | a0003c0003t0001g0072a0003c0003t0001g0098a0003c0003t0001g0115 | 3 | HG01346.hp1 HG01928.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.13+14489G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251128 | ||||||
| chr12:120251354
|
C | A | 6 | a0001c0001t0001g0214a0001c0013t0001g0213a0001c0013t0001g0215others(3): Show | 6 | HG02257.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+14263G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251354 | ||||||
| chr12:120251577
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.13+14040C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251577 | ||||||
| chr12:120251668
|
T | C | 6 | a0001c0001t0002g0069a0001c0005t0001g0044a0001c0005t0001g0047others(3): Show | 6 | HG02280.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.13+13949A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251668 | ||||||
| chr12:120251675
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+13942C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251675 | ||||||
| chr12:120251677
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01891.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.13+13940G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251677 | ||||||
| chr12:120251941
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.13+13676G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120251941 | ||||||
| chr12:120252115
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.13+13502G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252115 | ||||||
| chr12:120252320
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+13297C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252320 | ||||||
| chr12:120252405
|
T | C | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+13212A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252405 | ||||||
| chr12:120252693
|
A | T | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+12924T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252693 | ||||||
| chr12:120252708
|
C | G | 1 | a0002c0002t0001g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.13+12909G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252708 | ||||||
| chr12:120252859
|
G | A | 15 | a0001c0001t0002g0006a0001c0001t0002g0033a0001c0001t0002g0121others(12): Show | 18 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+12758C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252859 | ||||||
| chr12:120252998
|
C | CA | 19 | a0001c0001t0001g0222a0001c0001t0001g0227a0001c0001t0001g0261others(16): Show | 19 | HG00558.hp2 HG00741.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.13+12618dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252998 | ||||||
| chr12:120252998
|
CA | C | 36 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(33): Show | 41 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.13+12618delT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120252998 | ||||||
| chr12:120253307
|
T | C | 1 | a0001c0001t0002g0166 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.13+12310A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253307 | ||||||
| chr12:120253338
|
T | C | 1 | a0001c0010t0003g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.13+12279A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253338 | ||||||
| chr12:120253346
|
G | T | 60 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(57): Show | 65 | HG00408.hp2 HG01099.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.13+12271C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253346 | ||||||
| chr12:120253379
|
A | G | 1 | a0001c0001t0006g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.13+12238T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253379 | ||||||
| chr12:120253405
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0125 | 3 | HG03017.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.13+12212C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253405 | ||||||
| chr12:120253454
|
C | G | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+12163G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253454 | ||||||
| chr12:120253621
|
A | C | 61 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(58): Show | 66 | HG00408.hp2 HG01099.hp1 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.13+11996T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253621 | ||||||
| chr12:120253749
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.13+11868T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253749 | ||||||
| chr12:120253835
|
T | C | 2 | a0001c0010t0003g0211a0001c0010t0003g0212 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.13+11782A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253835 | ||||||
| chr12:120253905
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+11712C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120253905 | ||||||
| chr12:120254117
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.13+11500C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120254117 | ||||||
| chr12:120254362
|
G | T | 1 | a0001c0001t0002g0126 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.13+11255C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120254362 | ||||||
| chr12:120254376
|
C | T | 11 | a0001c0001t0001g0081a0001c0001t0010g0083a0001c0024t0001g0082others(8): Show | 12 | HG00099.hp1 HG02717.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.13+11241G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120254376 | ||||||
| chr12:120254693
|
G | C | 1 | a0001c0001t0002g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.13+10924C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120254693 | ||||||
| chr12:120254844
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.13+10773G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120254844 | ||||||
| chr12:120254924
|
A | G | 2 | a0001c0005t0001g0047a0001c0005t0001g0048 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.13+10693T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120254924 | ||||||
| chr12:120255101
|
G | A | 16 | a0001c0001t0002g0012a0001c0001t0002g0014a0001c0001t0002g0020others(13): Show | 19 | HG01433.hp2 HG01978.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.13+10516C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120255101 | ||||||
| chr12:120255485
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 166 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.13+10132T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120255485 | ||||||
| chr12:120255517
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.13+10100T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120255517 | ||||||
| chr12:120255825
|
T | G | 1 | a0001c0030t0004g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.13+9792A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120255825 | ||||||
| chr12:120255972
|
G | A | 3 | a0001c0001t0002g0177a0001c0006t0001g0169a0002c0002t0001g0168 | 3 | HG02280.hp2 HG02486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.13+9645C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120255972 | ||||||
| chr12:120256113
|
A | T | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+9504T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256113 | ||||||
| chr12:120256132
|
G | T | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.13+9485C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256132 | ||||||
| chr12:120256240
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.13+9377C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256240 | ||||||
| chr12:120256421
|
G | A | 1 | a0002c0002t0001g0264 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.13+9196C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256421 | ||||||
| chr12:120256487
|
A | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 170 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.13+9130T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256487 | ||||||
| chr12:120256499
|
T | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+9118A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256499 | ||||||
| chr12:120256501
|
G | C | 3 | a0001c0001t0001g0171a0001c0001t0002g0170a0001c0029t0002g0122 | 3 | HG02683.hp1 HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.13+9116C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256501 | ||||||
| chr12:120256641
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.13+8976G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256641 | ||||||
| chr12:120256697
|
C | G | 1 | a0001c0001t0003g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.13+8920G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256697 | ||||||
| chr12:120256718
|
G | T | 20 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(17): Show | 27 | HG01978.hp1 HG02109.hp1 HG02165.hp1 others(24): Show |
intron_variant | MODIFIER | c.13+8899C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256718 | ||||||
| chr12:120256780
|
T | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0265a0001c0001t0001g0266others(2): Show | 6 | HG00642.hp2 HG01168.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.13+8837A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256780 | ||||||
| chr12:120256804
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.13+8813C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256804 | ||||||
| chr12:120256820
|
G | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 128 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.13+8797C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256820 | ||||||
| chr12:120256867
|
G | A | 2 | a0001c0030t0004g0173a0002c0002t0001g0172 | 2 | HG01884.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.13+8750C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256867 | ||||||
| chr12:120256906
|
G | T | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+8711C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256906 | ||||||
| chr12:120256985
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 102 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.13+8632C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256985 | ||||||
| chr12:120256999
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 32 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.13+8618C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120256999 | ||||||
| chr12:120257012
|
C | T | 2 | a0001c0001t0002g0175a0001c0001t0007g0176 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.13+8605G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257012 | ||||||
| chr12:120257179
|
T | G | 1 | a0002c0002t0001g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.13+8438A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257179 | ||||||
| chr12:120257205
|
T | C | 1 | a0005c0008t0001g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.13+8412A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257205 | ||||||
| chr12:120257338
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 168 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.13+8279A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257338 | ||||||
| chr12:120257351
|
C | G | 1 | a0001c0017t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.13+8266G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257351 | ||||||
| chr12:120257394
|
C | G | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+8223G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257394 | ||||||
| chr12:120257401
|
C | T | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+8216G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257401 | ||||||
| chr12:120257405
|
C | T | 2 | a0001c0001t0002g0178a0008c0028t0001g0225 | 2 | HG01928.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.13+8212G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257405 | ||||||
| chr12:120257406
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.13+8211C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257406 | ||||||
| chr12:120257445
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 95 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.13+8172C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257445 | ||||||
| chr12:120257458
|
G | A | 1 | a0001c0006t0001g0041 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.13+8159C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257458 | ||||||
| chr12:120257461
|
G | T | 1 | a0003c0003t0001g0095 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.13+8156C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257461 | ||||||
| chr12:120257649
|
T | C | 1 | a0003c0003t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.13+7968A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257649 | ||||||
| chr12:120257654
|
T | C | 1 | a0002c0002t0001g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.13+7963A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257654 | ||||||
| chr12:120257865
|
C | G | 1 | a0001c0001t0002g0012 | 2 | NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.13+7752G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257865 | ||||||
| chr12:120257882
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0279 | 2 | HG00544.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.13+7735C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257882 | ||||||
| chr12:120257957
|
C | A | 29 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 34 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.13+7660G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257957 | ||||||
| chr12:120257964
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13+7653C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257964 | ||||||
| chr12:120257967
|
C | T | 1 | a0001c0005t0001g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.13+7650G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120257967 | ||||||
| chr12:120258018
|
C | A | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+7599G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258018 | ||||||
| chr12:120258162
|
C | T | 1 | a0001c0029t0002g0122 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.13+7455G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258162 | ||||||
| chr12:120258192
|
C | CA | 6 | a0001c0001t0001g0011a0001c0001t0001g0203a0001c0001t0002g0185others(3): Show | 7 | HG01168.hp1 HG01169.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.13+7424dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258192 | ||||||
| chr12:120258192
|
CA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 97 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.13+7424delT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258192 | ||||||
| chr12:120258432
|
G | C | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+7185C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258432 | ||||||
| chr12:120258442
|
G | A | 2 | a0001c0001t0002g0175a0001c0001t0007g0176 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.13+7175C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258442 | ||||||
| chr12:120258546
|
C | A | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+7071G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258546 | ||||||
| chr12:120258628
|
A | G | 1 | a0002c0012t0001g0009 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.13+6989T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258628 | ||||||
| chr12:120258721
|
C | A | 1 | a0001c0001t0002g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13+6896G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258721 | ||||||
| chr12:120258849
|
C | G | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+6768G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120258849 | ||||||
| chr12:120259081
|
A | C | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.13+6536T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259081 | ||||||
| chr12:120259082
|
C | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.13+6535G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259082 | ||||||
| chr12:120259082
|
CA | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 96 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.13+6534delT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259082 | ||||||
| chr12:120259196
|
A | T | 1 | a0001c0004t0001g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.13+6421T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259196 | ||||||
| chr12:120259199
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.13+6418G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259199 | ||||||
| chr12:120259332
|
C | T | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+6285G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259332 | ||||||
| chr12:120259333
|
A | C | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+6284T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259333 | ||||||
| chr12:120259441
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.13+6176A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259441 | ||||||
| chr12:120259614
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.13+6003G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259614 | ||||||
| chr12:120259667
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(71): Show | 94 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.13+5950C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259667 | ||||||
| chr12:120259733
|
C | A | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.13+5884G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259733 | ||||||
| chr12:120259954
|
C | T | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+5663G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120259954 | ||||||
| chr12:120260051
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.13+5566G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260051 | ||||||
| chr12:120260185
|
C | T | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+5432G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260185 | ||||||
| chr12:120260191
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.13+5426G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260191 | ||||||
| chr12:120260276
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.13+5341C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260276 | ||||||
| chr12:120260308
|
G | A | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+5309C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260308 | ||||||
| chr12:120260363
|
G | T | 1 | a0001c0001t0001g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.13+5254C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260363 | ||||||
| chr12:120260451
|
C | T | 9 | a0001c0001t0001g0205a0001c0001t0003g0204a0001c0001t0003g0206others(6): Show | 9 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.13+5166G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260451 | ||||||
| chr12:120260452
|
G | A | 10 | a0001c0001t0002g0020a0001c0001t0002g0028a0001c0001t0002g0093others(7): Show | 11 | HG01433.hp2 HG01978.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.13+5165C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260452 | ||||||
| chr12:120260487
|
G | C | 1 | a0002c0002t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.13+5130C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260487 | ||||||
| chr12:120260500
|
G | GA | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.13+5116dupT | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260500 | ||||||
| chr12:120260500
|
G | GAA | 7 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0002g0184others(4): Show | 7 | HG01433.hp2 HG02004.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.13+5115_13+5116dup others(2): Show |
PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260500 | ||||||
| chr12:120260587
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(73): Show | 96 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.13+5030C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260587 | ||||||
| chr12:120260665
|
A | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0218a0001c0001t0001g0219 | 4 | NA18945.hp1 NA18950.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+4952T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260665 | ||||||
| chr12:120260833
|
G | A | 9 | a0001c0001t0001g0205a0001c0001t0003g0204a0001c0001t0003g0206others(6): Show | 9 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.13+4784C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260833 | ||||||
| chr12:120260928
|
A | T | 1 | a0001c0001t0002g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.13+4689T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260928 | ||||||
| chr12:120260965
|
G | T | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+4652C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120260965 | ||||||
| chr12:120261116
|
T | C | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+4501A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261116 | ||||||
| chr12:120261140
|
A | G | 29 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 34 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.13+4477T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261140 | ||||||
| chr12:120261337
|
C | G | 4 | a0001c0004t0008g0040a0001c0006t0001g0038a0001c0006t0001g0039others(1): Show | 4 | HG02559.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+4280G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261337 | ||||||
| chr12:120261377
|
G | T | 1 | a0001c0001t0001g0277 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.13+4240C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261377 | ||||||
| chr12:120261388
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.13+4229T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261388 | ||||||
| chr12:120261487
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 95 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.13+4130C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261487 | ||||||
| chr12:120261536
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | NA18971.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.13+4081C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261536 | ||||||
| chr12:120261581
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.13+4036G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261581 | ||||||
| chr12:120261592
|
C | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 95 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.13+4025G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120261592 | ||||||
| chr12:120262093
|
A | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(15): Show | 23 | HG00408.hp2 HG02129.hp2 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.13+3524T>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262093 | ||||||
| chr12:120262249
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.13+3368G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262249 | ||||||
| chr12:120262285
|
C | G | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+3332G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262285 | ||||||
| chr12:120262325
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.13+3292G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262325 | ||||||
| chr12:120262509
|
C | T | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+3108G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262509 | ||||||
| chr12:120262686
|
C | T | 24 | a0001c0001t0001g0011a0001c0001t0001g0073a0001c0001t0001g0081others(21): Show | 27 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.13+2931G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262686 | ||||||
| chr12:120262728
|
A | C | 29 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 34 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.13+2889T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262728 | ||||||
| chr12:120262779
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.13+2838G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262779 | ||||||
| chr12:120262984
|
A | G | 1 | a0001c0001t0003g0280 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.13+2633T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120262984 | ||||||
| chr12:120263016
|
A | G | 2 | a0006c0009t0004g0034a0006c0009t0004g0035 | 2 | HG00438.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.13+2601T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263016 | ||||||
| chr12:120263069
|
G | A | 1 | a0002c0019t0001g0278 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.13+2548C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263069 | ||||||
| chr12:120263123
|
G | C | 1 | a0001c0001t0002g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13+2494C>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263123 | ||||||
| chr12:120263213
|
T | C | 1 | a0001c0017t0001g0070 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.13+2404A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263213 | ||||||
| chr12:120263259
|
G | A | 1 | a0001c0001t0002g0187 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.13+2358C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263259 | ||||||
| chr12:120263278
|
C | T | 1 | a0003c0003t0001g0072 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.13+2339G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263278 | ||||||
| chr12:120263491
|
T | G | 1 | a0001c0001t0001g0279 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.13+2126A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263491 | ||||||
| chr12:120263756
|
T | C | 1 | a0001c0001t0005g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.13+1861A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263756 | ||||||
| chr12:120263761
|
T | C | 1 | a0012c0016t0002g0189 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.13+1856A>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263761 | ||||||
| chr12:120263824
|
A | G | 1 | a0001c0001t0002g0071 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.13+1793T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263824 | ||||||
| chr12:120263961
|
C | G | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(143): Show | 171 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.13+1656G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120263961 | ||||||
| chr12:120264032
|
A | C | 3 | a0001c0001t0001g0214a0001c0013t0001g0213a0001c0013t0001g0215 | 3 | HG02572.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.13+1585T>G | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264032 | ||||||
| chr12:120264279
|
G | A | 1 | a0001c0001t0003g0280 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.13+1338C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264279 | ||||||
| chr12:120264443
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.13+1174C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264443 | ||||||
| chr12:120264468
|
G | A | 1 | a0010c0027t0013g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.13+1149C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264468 | ||||||
| chr12:120264492
|
G | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01891.hp1 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.13+1125C>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264492 | ||||||
| chr12:120264818
|
G | A | 27 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 32 | HG00408.hp2 HG01099.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.13+799C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264818 | ||||||
| chr12:120264958
|
T | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 97 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.13+659A>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264958 | ||||||
| chr12:120264972
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 97 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.13+645T>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120264972 | ||||||
| chr12:120265116
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(74): Show | 97 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.13+501C>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120265116 | ||||||
| chr12:120265234
|
C | A | 1 | a0001c0001t0003g0281 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.13+383G>T | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120265234 | ||||||
| chr12:120265361
|
C | T | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.13+256G>A | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120265361 | ||||||
| chr12:120265429
|
C | G | 1 | a0001c0001t0002g0028 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.13+188G>C | PXN | ENSG00000089159.17 | transcript | ENST00000637617.2 | protein_coding | 1/14 | chr12 | 120265429 |