Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10956 |
|---|---|
| ensemblid | ENSG00000135506.17 |
| hgncid | 16994 |
| symbol | OS9 |
| name | OS9 endoplasmic reticulum lectin |
| refseq_nuc | NM_006812.4 |
| refseq_prot | NP_006803.1 |
| ensembl_nuc | ENST00000315970.12 |
| ensembl_prot | ENSP00000318165.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 57694132 |
| end | 57721557 |
| strand | + |
| ver | v1.2 |
| region | chr12:57694132-57721557 |
| region5000 | chr12:57689132-57726557 |
| regionname0 | OS9_chr12_57694132_57721557 |
| regionname5000 | OS9_chr12_57689132_57726557 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 667 | 338 | 93 | 64 | 123 | 14 | 42 | 87 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0002 | 0/0 | 667 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0003 | 0/0 | 667 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0004 | 0/0 | 667 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0005 | 0/0 | 598 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0006 | 0/0 | 667 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0007 | 0/0 | 667 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0008 | 0/0 | 667 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2004 | 228 | 57 | 46 | 91 | 9 | 24 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0002 | 0/1 | 2004 | 97 | 26 | 17 | 32 | 5 | 16 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0003 | 0/0 | 2004 | 9 | 8 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0004 | 0/0 | 2004 | 6 | 0 | 0 | 6 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0005 | 0/0 | 2004 | 3 | 2 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0006 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0007 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0008 | 0/0 | 1994 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0009 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0010 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0011 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0012 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0013 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| c0014 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 679 | 234 | 59 | 47 | 92 | 9 | 26 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| t0002 | 0/1 | 679 | 112 | 32 | 20 | 38 | 5 | 16 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| t0003 | 0/0 | 679 | 4 | 4 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| t0004 | 0/0 | 679 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| t0005 | 0/0 | 679 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 8 | 1 | 3 | 3 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0002 | 0/0 | 8 | 1 | 5 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0003 | 0/0 | 6 | 1 | 2 | 1 | 1 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0007 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2004 | 228 | 57 | 46 | 91 | 9 | 24 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0002 | 0/1 | 2004 | 97 | 26 | 17 | 32 | 5 | 16 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0003 | 0/0 | 2004 | 9 | 8 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0006 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0010 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0011 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0013 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0002c0004 | 0/0 | 2004 | 6 | 0 | 0 | 6 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0003c0005 | 0/0 | 2004 | 3 | 2 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0004c0014 | 0/0 | 2004 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0005c0008 | 0/0 | 1994 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0006c0009 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0007c0007 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0008c0012 | 0/0 | 2004 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2682 | 227 | 57 | 45 | 91 | 9 | 24 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0001t0005 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0002t0002 | 0/1 | 2682 | 93 | 22 | 17 | 32 | 5 | 16 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0002t0003 | 0/0 | 2682 | 4 | 4 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0003t0002 | 0/0 | 2682 | 9 | 8 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0006t0001 | 0/0 | 2682 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0010t0001 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0011t0001 | 0/0 | 2682 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0001c0013t0001 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0002c0004t0002 | 0/0 | 2682 | 6 | 0 | 0 | 6 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0003c0005t0002 | 0/0 | 2682 | 3 | 2 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0004c0014t0004 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0005c0008t0001 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0006c0009t0001 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0007c0007t0002 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| a0008c0012t0001 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | copy fasta | chr12 | 57689132 | 57726557 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 1 | 3 | 3 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0002 | 0/0 | 8 | 1 | 5 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0003 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0235 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0006t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0010t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0011t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0013t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0003c0005t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0003c0005t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0003c0005t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0004c0014t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0005c0008t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0006c0009t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0007c0007t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0008c0012t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0003 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0239 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0263 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0160 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0247 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0190 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0234 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0230 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0257 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01167 | hp2 | a0006 | c0009 | t0001 | g0009 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0246 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0244 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0179 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0188 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01243 | hp2 | a0003 | c0005 | t0002 | g0030 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0192 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0207 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0260 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01361 | hp1 | a0007 | c0007 | t0002 | g0201 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0035 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0197 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01891 | hp1 | a0001 | c0010 | t0001 | g0112 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0184 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0175 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | CDX | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CDX | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02280 | hp1 | a0003 | c0005 | t0002 | g0178 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02300 | hp1 | a0008 | c0012 | t0001 | g0007 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02572 | hp2 | a0004 | c0014 | t0004 | g0052 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0203 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0174 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0025 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02683 | hp2 | a0001 | c0006 | t0001 | g0053 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0183 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0196 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0182 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0187 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0215 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0180 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0185 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0011 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0027 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0218 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03486 | hp2 | a0001 | c0013 | t0001 | g0116 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0025 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03540 | hp2 | a0003 | c0005 | t0002 | g0003 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0221 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0161 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03654 | hp2 | a0001 | c0011 | t0001 | g0037 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0231 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0242 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0220 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0200 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0217 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18940 | hp2 | a0002 | c0004 | t0002 | g0212 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18947 | hp1 | a0002 | c0004 | t0002 | g0012 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18970 | hp2 | a0002 | c0004 | t0002 | g0012 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0209 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18985 | hp2 | a0002 | c0004 | t0002 | g0191 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18997 | hp1 | a0002 | c0004 | t0002 | g0213 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18997 | hp2 | a0005 | c0008 | t0001 | g0163 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0193 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19055 | hp2 | a0002 | c0004 | t0002 | g0198 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0214 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0186 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0262 | AFR | ASW | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0233 | EUR | TSI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | GIH | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0194 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0259 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0235 | REF | REF | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0105 | REF | REF | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694175
|
C | G | 1 | a0004 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.14C>G | p.Thr5Arg | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 44/2682 | 14/2004 | 5/667 | chr12 | 57694175 | ||
| chr12:57694900
|
A | G | 1 | a0008 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.313A>G | p.Met105Val | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/15 | 343/2682 | 313/2004 | 105/667 | chr12 | 57694900 | ||
| chr12:57716432
|
G | A | 1 | a0002 | 6 | NA18940.hp2 NA18947.hp1 NA18970.hp2 others(3): Show |
missense_variant | MODERATE | c.913G>A | p.Asp305Asn | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 8/15 | 943/2682 | 913/2004 | 305/667 | chr12 | 57716432 | ||
| chr12:57718278
|
G | A | 1 | a0007 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1267G>A | p.Glu423Lys | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/15 | 1297/2682 | 1267/2004 | 423/667 | chr12 | 57718278 | ||
| chr12:57718372
|
C | T | 1 | a0003 | 3 | HG01243.hp2 HG02280.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.1361C>T | p.Ser454Leu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/15 | 1391/2682 | 1361/2004 | 454/667 | chr12 | 57718372 | ||
| chr12:57720435
|
TGGGCTGA others(3): Show |
T | 1 | a0005 | 1 | NA18997.hp2 | frameshift_variant | HIGH | c.1797_1806delGGCTGA others(4): Show |
p.Trp599fs | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/15 | 1827/2682 | 1797/2004 | 599/667 | INFO_REALIGN_3_PRIME | chr12 | 57720435 | |
| chr12:57720496
|
A | G | 1 | a0005 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1856A>G | p.Lys619Arg | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/15 | 1886/2682 | 1856/2004 | 619/667 | chr12 | 57720496 | ||
| chr12:57720514
|
T | G | 1 | a0005 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1874T>G | p.Ile625Ser | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/15 | 1904/2682 | 1874/2004 | 625/667 | chr12 | 57720514 | ||
| chr12:57720851
|
G | A | 1 | a0006 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.1946G>A | p.Arg649Gln | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 1976/2682 | 1946/2004 | 649/667 | chr12 | 57720851 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694207
|
C | T | 1 | a0001c0013 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.46C>T | p.Leu16Leu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 76/2682 | 46/2004 | 16/667 | chr12 | 57694207 | ||
| chr12:57694302
|
G | A | 1 | a0001c0003 | 9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.141G>A | p.Pro47Pro | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 171/2682 | 141/2004 | 47/667 | chr12 | 57694302 | ||
| chr12:57715924
|
T | G | 1 | a0001c0006 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.744T>G | p.Pro248Pro | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 6/15 | 774/2682 | 744/2004 | 248/667 | chr12 | 57715924 | ||
| chr12:57717883
|
C | T | 1 | a0001c0011 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1059C>T | p.Asn353Asn | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 10/15 | 1089/2682 | 1059/2004 | 353/667 | chr12 | 57717883 | ||
| chr12:57718406
|
A | G | 6 | a0001c0002a0001c0003a0002c0004others(3): Show | 117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
synonymous_variant | LOW | c.1395A>G | p.Glu465Glu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/15 | 1425/2682 | 1395/2004 | 465/667 | chr12 | 57718406 | ||
| chr12:57719082
|
C | T | 1 | a0001c0010 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1500C>T | p.Leu500Leu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/15 | 1530/2682 | 1500/2004 | 500/667 | chr12 | 57719082 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694143
|
A | G | 1 | a0001c0001t0005 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 19 | chr12 | 57694143 | |||||
| chr12:57721382
|
C | T | 1 | a0004c0014t0004 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*473C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 473 | chr12 | 57721382 | |||||
| chr12:57721426
|
C | G | 1 | a0001c0002t0003 | 4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*517C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 517 | chr12 | 57721426 | |||||
| chr12:57721488
|
T | C | 5 | a0001c0002t0002a0001c0003t0002a0002c0004t0002others(2): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*579T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 579 | chr12 | 57721488 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694554
|
C | T | 2 | a0001c0001t0001g0281a0001c0001t0001g0282 | 2 | NA18943.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.163-196C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/14 | chr12 | 57694554 | ||||||
| chr12:57694622
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163-128T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/14 | chr12 | 57694622 | ||||||
| chr12:57694728
|
C | A | 2 | a0001c0002t0002g0040a0001c0002t0002g0041 | 2 | NA18959.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.163-22C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/14 | chr12 | 57694728 | ||||||
| chr12:57695048
|
A | T | 1 | a0001c0001t0001g0280 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.339+122A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695048 | ||||||
| chr12:57695228
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.339+302C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695228 | ||||||
| chr12:57695248
|
T | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.339+322T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695248 | ||||||
| chr12:57695460
|
T | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-320T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695460 | ||||||
| chr12:57695513
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.340-267C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695513 | ||||||
| chr12:57695595
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340-185A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695595 | ||||||
| chr12:57695596
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG01168.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.340-184G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695596 | ||||||
| chr12:57695630
|
A | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.340-150A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695630 | ||||||
| chr12:57695906
|
C | T | 10 | a0001c0001t0001g0026a0001c0001t0001g0165a0001c0001t0001g0166others(7): Show | 11 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.404-56C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 3/14 | chr12 | 57695906 | ||||||
| chr12:57695921
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0164a0005c0008t0001g0163 | 5 | NA18983.hp2 NA18997.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-41C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 3/14 | chr12 | 57695921 | ||||||
| chr12:57695946
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.404-16G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 3/14 | chr12 | 57695946 | ||||||
| chr12:57696209
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.481-66G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 4/14 | chr12 | 57696209 | ||||||
| chr12:57696268
|
T | C | 5 | a0001c0002t0002g0011a0001c0002t0002g0174a0001c0002t0002g0175others(2): Show | 7 | HG02056.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.481-7T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 4/14 | chr12 | 57696268 | ||||||
| chr12:57696449
|
AGTCGG | A | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0216others(71): Show | 90 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.579+78_579+82delTC others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57696449 | |||||
| chr12:57696451
|
T | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(56): Show | 76 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.579+78T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696451 | ||||||
| chr12:57696453
|
GGGGC | G | 14 | a0001c0002t0002g0040a0001c0002t0002g0041a0001c0002t0002g0188others(11): Show | 15 | HG00408.hp2 HG00621.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.579+84_579+87delCG others(2): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57696453 | |||||
| chr12:57696456
|
GCGGGGGC | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(32): Show | 51 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.579+84_579+90delCG others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696456 | ||||||
| chr12:57696457
|
C | G | 1 | a0001c0002t0003g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.579+84C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696457 | ||||||
| chr12:57696462
|
GC | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0228others(36): Show | 52 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.579+90delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696462 | ||||||
| chr12:57696463
|
C | A | 2 | a0001c0002t0002g0179a0003c0005t0002g0178 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.579+90C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696463 | ||||||
| chr12:57696463
|
C | G | 53 | a0001c0001t0001g0216a0001c0001t0001g0223a0001c0001t0001g0224others(50): Show | 57 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.579+90C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696463 | ||||||
| chr12:57696464
|
G | A | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+91G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696464 | ||||||
| chr12:57696518
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(53): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.579+145G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696518 | ||||||
| chr12:57696656
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.579+283C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696656 | ||||||
| chr12:57696727
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.579+354C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696727 | ||||||
| chr12:57696819
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0173 | 3 | HG02622.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.579+446C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696819 | ||||||
| chr12:57696939
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(255): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.579+566A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696939 | ||||||
| chr12:57697256
|
T | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0256a0001c0001t0005g0257 | 3 | HG00323.hp1 HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.579+883T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697256 | ||||||
| chr12:57697333
|
A | G | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+960A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697333 | ||||||
| chr12:57697365
|
A | C | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+992A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697365 | ||||||
| chr12:57697489
|
A | T | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1116A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697489 | ||||||
| chr12:57697612
|
T | C | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1239T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697612 | ||||||
| chr12:57697627
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0258 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.579+1254T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697627 | ||||||
| chr12:57697697
|
A | G | 3 | a0001c0001t0001g0255a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | NA18948.hp2 NA18965.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.579+1324A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697697 | ||||||
| chr12:57697862
|
A | AAC | 41 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0026others(38): Show | 46 | HG00558.hp1 HG00597.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.579+1516_579+1517d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACAC | 5 | a0001c0001t0001g0123a0001c0002t0003g0184a0001c0002t0003g0185others(2): Show | 5 | HG00408.hp1 HG01891.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1514_579+1517d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACAC | 23 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 37 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.579+1512_579+1517d others(8): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACACA others(1): Show |
5 | a0001c0001t0001g0122a0001c0001t0001g0223a0001c0001t0001g0228others(2): Show | 5 | HG00323.hp1 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1510_579+1517d others(10): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACACA others(3): Show |
8 | a0001c0001t0001g0255a0001c0001t0001g0276a0001c0001t0001g0277others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+1508_579+1517d others(12): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACACA others(5): Show |
25 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0216others(22): Show | 26 | HG00408.hp2 HG00733.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.579+1506_579+1517d others(14): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACACA others(7): Show |
15 | a0001c0002t0002g0012a0001c0002t0002g0040a0001c0002t0002g0041others(12): Show | 16 | HG00741.hp1 HG01070.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.579+1504_579+1517d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACACA others(9): Show |
41 | a0001c0002t0002g0003a0001c0002t0002g0011a0001c0002t0002g0013others(38): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.579+1502_579+1517d others(18): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACACA others(11): Show |
14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 19 | HG01081.hp2 HG01346.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+1500_579+1517d others(20): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | AACACACA others(13): Show |
5 | a0001c0001t0001g0044a0001c0002t0002g0199a0001c0002t0002g0230others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1498_579+1517d others(22): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | |||||
| chr12:57697862
|
A | ACACACAC others(8): Show |
1 | a0002c0004t0002g0198 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.579+1489_579+1490i others(17): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697862 | ||||||
| chr12:57697862
|
A | ACACACAC others(10): Show |
1 | a0001c0002t0002g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.579+1489_579+1490i others(19): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697862 | ||||||
| chr12:57697862
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+1489_579+1490i others(21): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697862 | ||||||
| chr12:57697889
|
A | G | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1516A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697889 | ||||||
| chr12:57697908
|
A | C | 1 | a0001c0002t0002g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1535A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697908 | ||||||
| chr12:57697908
|
AACACACA others(9): Show |
A | 8 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(5): Show | 8 | HG02055.hp1 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+1551_579+1566d others(18): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | |||||
| chr12:57697908
|
AACACACA others(11): Show |
A | 12 | a0001c0001t0001g0229a0001c0002t0002g0014a0001c0002t0002g0034others(9): Show | 15 | HG01243.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.579+1551_579+1568d others(20): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | |||||
| chr12:57697908
|
AACACACA others(13): Show |
A | 34 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0122others(31): Show | 39 | HG00621.hp1 HG00733.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.579+1551_579+1570d others(22): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | |||||
| chr12:57697908
|
AACACACA others(15): Show |
A | 83 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.579+1551_579+1572d others(24): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | |||||
| chr12:57697908
|
AACACACA others(17): Show |
A | 1 | a0001c0002t0002g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.579+1551_579+1574d others(26): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | |||||
| chr12:57697910
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+1551_579+1564d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697910 | |||||
| chr12:57697911
|
ACACACAC others(14): Show |
A | 1 | a0001c0001t0001g0275 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.579+1539_579+1559d others(23): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697911 | ||||||
| chr12:57697912
|
C | A | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1539C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697912 | ||||||
| chr12:57697924
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.579+1551T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697924 | ||||||
| chr12:57697924
|
T | TAC | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(38): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.579+1592_579+1593d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697924
|
T | TACAC | 27 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(24): Show | 30 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.579+1590_579+1593d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697924
|
T | TACACAC | 13 | a0001c0001t0001g0022a0001c0001t0001g0051a0001c0001t0001g0097others(10): Show | 14 | HG00642.hp1 HG01934.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+1588_579+1593d others(8): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697924
|
T | TACACACA others(1): Show |
7 | a0001c0001t0001g0039a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG02257.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+1586_579+1593d others(10): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697924
|
T | TACACACA others(3): Show |
1 | a0001c0001t0001g0057 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.579+1584_579+1593d others(12): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697924
|
TAC | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0018a0001c0001t0001g0086others(14): Show | 21 | HG00438.hp2 HG00558.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+1592_579+1593d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697924
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0094 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.579+1584_579+1593d others(12): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697924
|
TACACACA others(7): Show |
T | 11 | a0001c0001t0001g0020a0001c0001t0001g0114a0001c0001t0001g0115others(8): Show | 13 | HG00544.hp2 HG01496.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+1580_579+1593d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | |||||
| chr12:57697926
|
C | A | 1 | a0001c0002t0002g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1553C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697926 | ||||||
| chr12:57697927
|
A | G | 1 | a0001c0002t0002g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1554A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697927 | ||||||
| chr12:57697928
|
C | A | 3 | a0001c0003t0002g0193a0001c0003t0002g0196a0001c0003t0002g0214 | 3 | HG02809.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.579+1555C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697928 | ||||||
| chr12:57697930
|
C | A | 12 | a0001c0001t0001g0229a0001c0002t0002g0014a0001c0002t0002g0180others(9): Show | 14 | HG01243.hp1 HG01361.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+1557C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697930 | ||||||
| chr12:57697932
|
C | A | 33 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0216others(30): Show | 38 | HG00621.hp1 HG00733.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.579+1559C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697932 | ||||||
| chr12:57697934
|
C | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.579+1561C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697934 | ||||||
| chr12:57697936
|
C | A | 1 | a0001c0002t0002g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.579+1563C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697936 | ||||||
| chr12:57698071
|
A | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.579+1698A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698071 | ||||||
| chr12:57698175
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.579+1802T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698175 | ||||||
| chr12:57698216
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+1843C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698216 | ||||||
| chr12:57698230
|
C | A | 1 | a0001c0002t0002g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1857C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698230 | ||||||
| chr12:57698233
|
G | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG00140.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.579+1860G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698233 | ||||||
| chr12:57698305
|
C | CACTT | 145 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.579+1933_579+1936d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57698305 | |||||
| chr12:57698363
|
T | A | 1 | a0001c0002t0002g0180 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.579+1990T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698363 | ||||||
| chr12:57698673
|
C | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+2300C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698673 | ||||||
| chr12:57698734
|
G | T | 1 | a0001c0002t0002g0175 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.579+2361G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698734 | ||||||
| chr12:57698771
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.579+2398A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698771 | ||||||
| chr12:57699168
|
A | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+2795A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699168 | ||||||
| chr12:57699317
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.579+2944T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699317 | ||||||
| chr12:57699365
|
C | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0069 | 3 | HG03490.hp1 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.579+2992C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699365 | ||||||
| chr12:57699393
|
G | C | 1 | a0001c0001t0001g0114 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.579+3020G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699393 | ||||||
| chr12:57699710
|
T | G | 1 | a0001c0001t0001g0060 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.579+3337T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699710 | ||||||
| chr12:57699824
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.579+3451G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699824 | ||||||
| chr12:57699952
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 169 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.579+3579G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699952 | ||||||
| chr12:57700026
|
C | T | 1 | a0001c0001t0001g0258 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.579+3653C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700026 | ||||||
| chr12:57700034
|
G | A | 4 | a0001c0002t0002g0011a0001c0002t0002g0174a0001c0002t0002g0176others(1): Show | 6 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+3661G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700034 | ||||||
| chr12:57700037
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+3664G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700037 | ||||||
| chr12:57700052
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.579+3679A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700052 | ||||||
| chr12:57700279
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0159 | 2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.579+3906A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700279 | ||||||
| chr12:57700315
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+3942A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700315 | ||||||
| chr12:57700491
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0270a0001c0002t0002g0183 | 3 | HG01167.hp1 HG01175.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.579+4118G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700491 | ||||||
| chr12:57700714
|
C | T | 13 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0216others(10): Show | 14 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+4341C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700714 | ||||||
| chr12:57700939
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.579+4566C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700939 | ||||||
| chr12:57701026
|
T | A | 3 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0002t0002g0183 | 3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.579+4653T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701026 | ||||||
| chr12:57701081
|
C | CT | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.579+4708_579+4709i others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701081 | ||||||
| chr12:57701245
|
G | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+4872G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701245 | ||||||
| chr12:57701262
|
A | AT | 10 | a0001c0001t0001g0019a0001c0001t0001g0081a0001c0001t0001g0099others(7): Show | 11 | HG00621.hp2 HG00738.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.579+4920dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | |||||
| chr12:57701262
|
AT | A | 36 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0018others(33): Show | 42 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.579+4920delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | |||||
| chr12:57701262
|
ATT | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 87 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.579+4919_579+4920d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | |||||
| chr12:57701262
|
ATTT | A | 9 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0058others(6): Show | 9 | HG01168.hp2 HG02055.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+4918_579+4920d others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | |||||
| chr12:57701262
|
ATTTTTTT | A | 28 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0229others(25): Show | 30 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+4914_579+4920d others(9): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | |||||
| chr12:57701262
|
ATTTTTTT others(1): Show |
A | 102 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.579+4913_579+4920d others(10): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | |||||
| chr12:57701303
|
T | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+4930T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701303 | ||||||
| chr12:57701432
|
C | T | 1 | a0001c0002t0002g0259 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.579+5059C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701432 | ||||||
| chr12:57701439
|
T | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+5066T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701439 | ||||||
| chr12:57701468
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+5095G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701468 | ||||||
| chr12:57701627
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.579+5254T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701627 | ||||||
| chr12:57701658
|
C | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+5285C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701658 | ||||||
| chr12:57701788
|
G | GTTTGT | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.579+5434_579+5438d others(7): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701788 | |||||
| chr12:57701793
|
T | TTTTGC | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 14 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.579+5424_579+5425i others(7): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701793 | |||||
| chr12:57701817
|
A | G | 1 | a0001c0002t0002g0041 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.579+5444A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701817 | ||||||
| chr12:57701986
|
G | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5613G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701986 | ||||||
| chr12:57702028
|
A | G | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+5655A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702028 | ||||||
| chr12:57702038
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.579+5665G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702038 | ||||||
| chr12:57702134
|
AG | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5762delG | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702134 | ||||||
| chr12:57702206
|
T | C | 80 | a0001c0002t0002g0003a0001c0002t0002g0011a0001c0002t0002g0012others(77): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.579+5833T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702206 | ||||||
| chr12:57702210
|
C | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+5837C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702210 | ||||||
| chr12:57702270
|
G | T | 1 | a0001c0002t0002g0180 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.579+5897G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702270 | ||||||
| chr12:57702302
|
C | G | 1 | a0001c0002t0002g0208 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.579+5929C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702302 | ||||||
| chr12:57702364
|
T | C | 1 | a0001c0002t0002g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.579+5991T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702364 | ||||||
| chr12:57702606
|
G | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+6233G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702606 | ||||||
| chr12:57703741
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.579+7368A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703741 | ||||||
| chr12:57703762
|
AT | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 156 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.579+7400delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57703762 | |||||
| chr12:57703762
|
ATT | A | 17 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0216others(14): Show | 18 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.579+7399_579+7400d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57703762 | |||||
| chr12:57703832
|
C | T | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+7459C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703832 | ||||||
| chr12:57703903
|
G | A | 3 | a0001c0002t0002g0217a0001c0002t0002g0220a0001c0002t0002g0250 | 3 | HG03710.hp1 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.579+7530G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703903 | ||||||
| chr12:57703967
|
A | G | 25 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0123others(22): Show | 29 | HG00408.hp1 HG00558.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.579+7594A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703967 | ||||||
| chr12:57704079
|
T | C | 108 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0216others(105): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.579+7706T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704079 | ||||||
| chr12:57704100
|
A | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG00140.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.579+7727A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704100 | ||||||
| chr12:57704334
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.579+7961C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704334 | ||||||
| chr12:57704406
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0095a0001c0001t0001g0096others(13): Show | 17 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.579+8033G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704406 | ||||||
| chr12:57704429
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.579+8056C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704429 | ||||||
| chr12:57704437
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.579+8064C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704437 | ||||||
| chr12:57704537
|
C | CA | 79 | a0001c0002t0002g0003a0001c0002t0002g0011a0001c0002t0002g0012others(76): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.579+8175dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57704537 | |||||
| chr12:57704619
|
A | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | NA18948.hp2 NA18965.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.579+8246A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704619 | ||||||
| chr12:57704620
|
G | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | NA18948.hp2 NA18965.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.579+8247G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704620 | ||||||
| chr12:57704631
|
T | C | 4 | a0001c0002t0002g0011a0001c0002t0002g0174a0001c0002t0002g0176others(1): Show | 6 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+8258T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704631 | ||||||
| chr12:57704642
|
A | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.579+8269A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704642 | ||||||
| chr12:57704643
|
G | A | 1 | a0001c0002t0002g0204 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.579+8270G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704643 | ||||||
| chr12:57704643
|
G | T | 1 | a0001c0002t0002g0175 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.579+8270G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704643 | ||||||
| chr12:57704963
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 41 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.579+8590C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704963 | ||||||
| chr12:57705315
|
C | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+8942C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705315 | ||||||
| chr12:57705445
|
CTT | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+9073_579+9074d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705445 | ||||||
| chr12:57705581
|
C | G | 2 | a0001c0002t0002g0033a0001c0002t0002g0261 | 3 | HG02451.hp1 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.579+9208C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705581 | ||||||
| chr12:57705600
|
C | T | 1 | a0001c0002t0002g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.579+9227C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705600 | ||||||
| chr12:57705617
|
C | T | 1 | a0001c0002t0002g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579+9244C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705617 | ||||||
| chr12:57705673
|
G | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+9300G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705673 | ||||||
| chr12:57705878
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.579+9505T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705878 | ||||||
| chr12:57705926
|
T | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+9553T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705926 | ||||||
| chr12:57705953
|
G | A | 80 | a0001c0002t0002g0003a0001c0002t0002g0011a0001c0002t0002g0012others(77): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.579+9580G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705953 | ||||||
| chr12:57706028
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.579+9655C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706028 | ||||||
| chr12:57706057
|
A | G | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+9684A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706057 | ||||||
| chr12:57706193
|
G | A | 8 | a0001c0003t0002g0027a0001c0003t0002g0193a0001c0003t0002g0194others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-9567G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706193 | ||||||
| chr12:57706275
|
T | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 167 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.580-9485T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706275 | ||||||
| chr12:57706528
|
G | A | 5 | a0001c0002t0002g0190a0001c0002t0002g0208a0001c0002t0002g0233others(2): Show | 5 | HG00140.hp2 HG01070.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-9232G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706528 | ||||||
| chr12:57706720
|
A | G | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-9040A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706720 | ||||||
| chr12:57706737
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.580-9023T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706737 | ||||||
| chr12:57706768
|
T | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.580-8992T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706768 | ||||||
| chr12:57706846
|
G | GA | 91 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 113 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.580-8891dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | |||||
| chr12:57706846
|
G | GAA | 91 | a0001c0001t0001g0043a0001c0001t0001g0153a0001c0001t0001g0168others(88): Show | 110 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.580-8892_580-8891d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | |||||
| chr12:57706846
|
G | GAAAAAAA others(9): Show |
2 | a0001c0002t0002g0025a0001c0002t0002g0161 | 3 | HG02683.hp1 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.580-8906_580-8891d others(18): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | |||||
| chr12:57706846
|
G | GAAAAAAA others(10): Show |
1 | a0001c0002t0002g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.580-8907_580-8891d others(19): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | |||||
| chr12:57706846
|
GA | G | 12 | a0001c0001t0001g0009a0001c0001t0001g0075a0001c0001t0001g0080others(9): Show | 13 | HG01167.hp2 HG02615.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-8891delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | |||||
| chr12:57706864
|
AAAAAAG | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-8895_580-8890d others(8): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706864 | ||||||
| chr12:57706870
|
G | A | 4 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161others(1): Show | 5 | HG00544.hp2 HG02572.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-8890G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706870 | ||||||
| chr12:57706900
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.580-8860A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706900 | ||||||
| chr12:57706927
|
G | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.580-8833G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706927 | ||||||
| chr12:57707074
|
A | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(271): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.580-8686A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707074 | ||||||
| chr12:57707186
|
G | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-8574G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707186 | ||||||
| chr12:57707516
|
C | T | 1 | a0001c0002t0002g0219 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.580-8244C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707516 | ||||||
| chr12:57707527
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-8233C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707527 | ||||||
| chr12:57707571
|
T | G | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-8189T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707571 | ||||||
| chr12:57707638
|
A | G | 1 | a0001c0002t0002g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.580-8122A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707638 | ||||||
| chr12:57707689
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0128others(8): Show | 15 | HG01358.hp2 HG01928.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.580-8071G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707689 | ||||||
| chr12:57707783
|
A | AT | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-7969dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57707783 | |||||
| chr12:57707802
|
A | C | 12 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0216others(9): Show | 13 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-7958A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707802 | ||||||
| chr12:57707929
|
G | GA | 83 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(80): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.580-7817dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57707929 | |||||
| chr12:57707936
|
A | G | 1 | a0001c0002t0002g0242 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.580-7824A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707936 | ||||||
| chr12:57707944
|
T | A | 1 | a0001c0002t0002g0240 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.580-7816T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707944 | ||||||
| chr12:57707964
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.580-7796G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707964 | ||||||
| chr12:57708009
|
C | G | 1 | a0001c0001t0001g0225 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.580-7751C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708009 | ||||||
| chr12:57708031
|
T | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0118 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.580-7729T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708031 | ||||||
| chr12:57708049
|
C | T | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-7711C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708049 | ||||||
| chr12:57708060
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.580-7700T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708060 | ||||||
| chr12:57708083
|
C | T | 8 | a0001c0001t0001g0135a0001c0001t0001g0137a0001c0001t0001g0151others(5): Show | 8 | HG01255.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-7677C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708083 | ||||||
| chr12:57708090
|
T | A | 2 | a0001c0002t0002g0199a0001c0002t0002g0230 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.580-7670T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708090 | ||||||
| chr12:57708276
|
A | AT | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.580-7477dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57708276 | |||||
| chr12:57708283
|
T | A | 1 | a0001c0002t0002g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.580-7477T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708283 | ||||||
| chr12:57708625
|
CA | C | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-7120delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57708625 | |||||
| chr12:57708767
|
C | T | 1 | a0001c0002t0002g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.580-6993C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708767 | ||||||
| chr12:57708956
|
T | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-6804T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708956 | ||||||
| chr12:57709264
|
T | G | 4 | a0001c0001t0001g0036a0001c0001t0001g0266a0001c0001t0001g0267others(1): Show | 5 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-6496T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709264 | ||||||
| chr12:57709352
|
T | C | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-6408T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709352 | ||||||
| chr12:57709541
|
A | T | 1 | a0001c0002t0002g0177 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.580-6219A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709541 | ||||||
| chr12:57709574
|
T | C | 2 | a0001c0003t0002g0193a0001c0003t0002g0214 | 2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.580-6186T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709574 | ||||||
| chr12:57709640
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.580-6120G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709640 | ||||||
| chr12:57709809
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.580-5951A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709809 | ||||||
| chr12:57709861
|
C | CT | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-5890dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57709861 | |||||
| chr12:57709906
|
G | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-5854G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709906 | ||||||
| chr12:57710015
|
G | C | 8 | a0001c0003t0002g0027a0001c0003t0002g0193a0001c0003t0002g0194others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-5745G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710015 | ||||||
| chr12:57710031
|
C | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-5729C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710031 | ||||||
| chr12:57710133
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-5627G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710133 | ||||||
| chr12:57710237
|
T | TA | 10 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 13 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-5521dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57710237 | |||||
| chr12:57710311
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.580-5449T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710311 | ||||||
| chr12:57710321
|
C | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.580-5439C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710321 | ||||||
| chr12:57710374
|
G | C | 1 | a0001c0002t0002g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.580-5386G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710374 | ||||||
| chr12:57710694
|
A | G | 23 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(20): Show | 27 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-5066A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710694 | ||||||
| chr12:57710715
|
C | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-5045C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710715 | ||||||
| chr12:57710853
|
C | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.580-4907C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710853 | ||||||
| chr12:57710996
|
A | G | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-4764A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710996 | ||||||
| chr12:57711038
|
C | CA | 80 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(77): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.580-4699dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | |||||
| chr12:57711038
|
C | CAA | 9 | a0001c0001t0001g0048a0001c0001t0001g0057a0001c0001t0001g0064others(6): Show | 9 | HG01433.hp1 HG02074.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-4700_580-4699d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | |||||
| chr12:57711038
|
CA | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0252a0001c0001t0001g0254others(5): Show | 8 | HG00597.hp2 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-4699delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | |||||
| chr12:57711038
|
CAA | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(125): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.580-4700_580-4699d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | |||||
| chr12:57711038
|
CAAA | C | 9 | a0001c0001t0001g0122a0001c0001t0001g0270a0001c0002t0002g0025others(6): Show | 10 | HG00544.hp2 HG01167.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-4701_580-4699d others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | |||||
| chr12:57711101
|
C | A | 13 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0216others(10): Show | 14 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-4659C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711101 | ||||||
| chr12:57711208
|
G | A | 4 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(1): Show | 4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4552G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711208 | ||||||
| chr12:57711292
|
T | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4468T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711292 | ||||||
| chr12:57711311
|
TAG | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(141): Show | 178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.580-4443_580-4442d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711311 | |||||
| chr12:57711338
|
C | CT | 8 | a0001c0001t0001g0114a0001c0001t0001g0151a0001c0001t0001g0153others(5): Show | 9 | HG01255.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-4396dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | |||||
| chr12:57711338
|
CT | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(110): Show | 140 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.580-4396delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | |||||
| chr12:57711338
|
CTTT | C | 10 | a0001c0001t0001g0265a0001c0001t0001g0274a0001c0002t0002g0179others(7): Show | 10 | HG00140.hp2 HG01192.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-4398_580-4396d others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | |||||
| chr12:57711338
|
CTTTT | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.580-4399_580-4396d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | |||||
| chr12:57711408
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0099 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.580-4352G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711408 | ||||||
| chr12:57711439
|
C | T | 1 | a0001c0002t0002g0211 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.580-4321C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711439 | ||||||
| chr12:57711472
|
G | A | 3 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0002t0002g0183 | 3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.580-4288G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711472 | ||||||
| chr12:57711481
|
G | GGACT | 4 | a0001c0001t0001g0009a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 5 | HG01167.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-4278_580-4275d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711481 | |||||
| chr12:57711512
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4248A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711512 | ||||||
| chr12:57711592
|
T | A | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4168T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711592 | ||||||
| chr12:57711592
|
T | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(252): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.580-4168T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711592 | ||||||
| chr12:57711665
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580-4095C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711665 | ||||||
| chr12:57711804
|
T | TTGGGCTG others(7): Show |
1 | a0001c0001t0001g0079 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.580-3952_580-3939d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711804 | |||||
| chr12:57711916
|
C | G | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-3844C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711916 | ||||||
| chr12:57711917
|
T | G | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-3843T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711917 | ||||||
| chr12:57711974
|
G | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0165 | 2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.580-3786G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711974 | ||||||
| chr12:57712066
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.580-3694G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712066 | ||||||
| chr12:57712286
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.580-3474C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712286 | ||||||
| chr12:57712333
|
G | A | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3427G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712333 | ||||||
| chr12:57712430
|
T | G | 1 | a0001c0002t0002g0217 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.580-3330T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712430 | ||||||
| chr12:57712495
|
TC | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.580-3264delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712495 | ||||||
| chr12:57712607
|
TATGTTTC others(18): Show |
T | 1 | a0001c0001t0001g0046 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.580-3142_580-3118d others(27): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57712607 | |||||
| chr12:57712710
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.580-3050C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712710 | ||||||
| chr12:57712768
|
T | C | 4 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(1): Show | 4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-2992T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712768 | ||||||
| chr12:57712851
|
G | A | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-2909G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712851 | ||||||
| chr12:57712976
|
G | A | 4 | a0001c0002t0003g0184a0001c0002t0003g0185a0001c0002t0003g0186others(1): Show | 4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-2784G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712976 | ||||||
| chr12:57713027
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.580-2733G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713027 | ||||||
| chr12:57713053
|
A | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.580-2707A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713053 | ||||||
| chr12:57713275
|
C | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-2485C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713275 | ||||||
| chr12:57713287
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.580-2473C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713287 | ||||||
| chr12:57713441
|
T | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0114a0001c0001t0001g0117others(3): Show | 7 | HG01496.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-2319T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713441 | ||||||
| chr12:57713493
|
C | T | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-2267C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713493 | ||||||
| chr12:57713526
|
CCT | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-2231_580-2230d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57713526 | |||||
| chr12:57713698
|
C | CT | 23 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0043others(20): Show | 26 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.580-2043dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57713698 | |||||
| chr12:57713698
|
CT | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0061a0001c0001t0001g0067others(7): Show | 11 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-2043delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57713698 | |||||
| chr12:57713706
|
T | TC | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-2054_580-2053i others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713706 | ||||||
| chr12:57713817
|
C | A | 1 | a0001c0001t0001g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.580-1943C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713817 | ||||||
| chr12:57713942
|
AC | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-1817delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713942 | ||||||
| chr12:57714269
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.580-1491C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714269 | ||||||
| chr12:57714270
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580-1490G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714270 | ||||||
| chr12:57714311
|
A | G | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-1449A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714311 | ||||||
| chr12:57714419
|
T | G | 140 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.580-1341T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714419 | ||||||
| chr12:57714636
|
C | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-1124C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714636 | ||||||
| chr12:57714660
|
A | T | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-1100A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714660 | ||||||
| chr12:57714736
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 41 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.580-1024C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714736 | ||||||
| chr12:57714757
|
C | T | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 14 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.580-1003C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714757 | ||||||
| chr12:57714828
|
A | G | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-932A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714828 | ||||||
| chr12:57715018
|
A | G | 1 | a0001c0002t0002g0237 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.580-742A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715018 | ||||||
| chr12:57715069
|
TA | T | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-683delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57715069 | |||||
| chr12:57715252
|
C | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-508C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715252 | ||||||
| chr12:57715269
|
C | T | 7 | a0001c0002t0002g0222a0001c0003t0002g0027a0001c0003t0002g0193others(4): Show | 8 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-491C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715269 | ||||||
| chr12:57715596
|
A | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0067a0001c0001t0001g0068 | 3 | HG00140.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.580-164A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715596 | ||||||
| chr12:57715654
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-106C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715654 | ||||||
| chr12:57716019
|
G | C | 8 | a0001c0002t0002g0013a0001c0002t0002g0029a0001c0002t0002g0195others(5): Show | 11 | HG00408.hp2 HG00544.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.790+49G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 6/14 | chr12 | 57716019 | ||||||
| chr12:57716020
|
G | T | 8 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.790+50G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 6/14 | chr12 | 57716020 | ||||||
| chr12:57716279
|
T | TG | 106 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0044others(103): Show | 130 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.892+95dupG | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 57716279 | |||||
| chr12:57716279
|
T | TGG | 21 | a0001c0001t0001g0008a0001c0001t0001g0038a0001c0001t0001g0224others(18): Show | 26 | HG00438.hp1 HG00738.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.892+94_892+95dupGG | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 57716279 | |||||
| chr12:57716281
|
G | GC | 4 | a0001c0002t0002g0014a0001c0002t0002g0033a0001c0002t0002g0034others(1): Show | 8 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.892+88_892+89insC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | chr12 | 57716281 | ||||||
| chr12:57716284
|
G | C | 1 | a0001c0001t0001g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.892+91G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | chr12 | 57716284 | ||||||
| chr12:57716315
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.893-97C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | chr12 | 57716315 | ||||||
| chr12:57717018
|
A | G | 1 | a0001c0002t0002g0243 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1045+274A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717018 | ||||||
| chr12:57717432
|
T | C | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1046-438T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717432 | ||||||
| chr12:57717602
|
G | A | 13 | a0001c0002t0002g0222a0001c0002t0003g0184a0001c0002t0003g0185others(10): Show | 14 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1046-268G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717602 | ||||||
| chr12:57717638
|
C | T | 8 | a0001c0003t0002g0027a0001c0003t0002g0193a0001c0003t0002g0194others(5): Show | 9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1046-232C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717638 | ||||||
| chr12:57717792
|
C | CA | 122 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1046-51dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | |||||
| chr12:57717792
|
C | CAA | 14 | a0001c0001t0001g0023a0001c0001t0001g0057a0001c0001t0001g0059others(11): Show | 15 | HG01358.hp1 HG01358.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046-52_1046-51dup others(2): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | |||||
| chr12:57717792
|
CAAA | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 38 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1046-53_1046-51del others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | |||||
| chr12:57717792
|
CAAAAAA | C | 7 | a0001c0002t0002g0226a0001c0002t0002g0236a0001c0002t0002g0246others(4): Show | 7 | HG00741.hp1 HG01168.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1046-56_1046-51del others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | |||||
| chr12:57717792
|
CAAAAAAA | C | 83 | a0001c0002t0002g0003a0001c0002t0002g0011a0001c0002t0002g0012others(80): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1046-57_1046-51del others(7): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | |||||
| chr12:57717988
|
AC | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0010t0001g0112 | 3 | HG01891.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1134+33delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 57717988 | |||||
| chr12:57718088
|
G | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1135-58G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 10/14 | chr12 | 57718088 | ||||||
| chr12:57718510
|
C | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0066a0001c0001t0001g0094 | 3 | HG00558.hp2 HG02523.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1410+89C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718510 | ||||||
| chr12:57718654
|
C | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 43 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1410+233C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718654 | ||||||
| chr12:57718794
|
CTTTGGAA others(25): Show |
C | 2 | a0001c0001t0001g0095a0001c0001t0001g0099 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1411-198_1411-167d others(34): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718794 | ||||||
| chr12:57718820
|
G | A | 2 | a0001c0002t0002g0181a0001c0002t0002g0182 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1411-173G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718820 | ||||||
| chr12:57718935
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1411-58C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718935 | ||||||
| chr12:57719342
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(277): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1600+160A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719342 | ||||||
| chr12:57719375
|
C | T | 92 | a0001c0002t0002g0003a0001c0002t0002g0011a0001c0002t0002g0012others(89): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1600+193C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719375 | ||||||
| chr12:57719484
|
T | C | 1 | a0001c0002t0002g0180 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1600+302T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719484 | ||||||
| chr12:57719633
|
C | A | 80 | a0001c0002t0002g0003a0001c0002t0002g0011a0001c0002t0002g0012others(77): Show | 94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1600+451C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719633 | ||||||
| chr12:57719776
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0165 | 2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1601-323C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719776 | ||||||
| chr12:57719847
|
T | C | 3 | a0001c0002t0002g0025a0001c0002t0002g0160a0001c0002t0002g0161 | 4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601-252T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719847 | ||||||
| chr12:57719886
|
C | T | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1601-213C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719886 | ||||||
| chr12:57720050
|
T | C | 1 | a0004c0014t0004g0052 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1601-49T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57720050 | ||||||
| chr12:57720092
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG00741.hp2 | splice_region_variant&intron_variant | LOW | c.1601-7C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57720092 | ||||||
| chr12:57720349
|
G | A | 1 | a0001c0001t0005g0257 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1766-57G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 13/14 | chr12 | 57720349 | ||||||
| chr12:57720522
|
A | G | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | splice_region_variant&intron_variant | LOW | c.1878+4A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720522 | ||||||
| chr12:57720531
|
T | G | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+13T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720531 | ||||||
| chr12:57720532
|
A | C | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+14A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720532 | ||||||
| chr12:57720537
|
C | T | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+19C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720537 | ||||||
| chr12:57720539
|
A | C | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+21A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720539 | ||||||
| chr12:57720540
|
G | C | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+22G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720540 | ||||||
| chr12:57720541
|
T | C | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+23T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720541 | ||||||
| chr12:57720547
|
C | T | 1 | a0005c0008t0001g0163 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+29C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720547 | ||||||
| chr12:57720570
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0159 | 3 | HG02055.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1878+52G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720570 | ||||||
| chr12:57720582
|
C | T | 1 | a0001c0002t0002g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1878+64C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720582 |