Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4135 |
|---|---|
| ensemblid | ENSG00000171533.12 |
| hgncid | 6868 |
| symbol | MAP6 |
| name | microtubule associated protein 6 |
| refseq_nuc | NM_033063.2 |
| refseq_prot | NP_149052.1 |
| ensembl_nuc | ENST00000304771.8 |
| ensembl_prot | ENSP00000307093.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 75586918 |
| end | 75669038 |
| strand | - |
| ver | v1.2 |
| region | chr11:75586918-75669038 |
| region5000 | chr11:75581918-75674038 |
| regionname0 | MAP6_chr11_75586918_75669038 |
| regionname5000 | MAP6_chr11_75581918_75674038 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 813 | 207 | 48 | 31 | 107 | 4 | 17 | 87 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002 | 1/0 | 813 | 172 | 35 | 25 | 82 | 6 | 23 | 65 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0003 | 0/1 | 813 | 4 | 0 | 0 | 2 | 1 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0004 | 0/0 | 813 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0005 | 0/0 | 813 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0006 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0007 | 0/0 | 813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0008 | 0/0 | 813 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0009 | 0/0 | 813 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2442 | 140 | 37 | 8 | 85 | 1 | 9 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0002 | 1/0 | 2442 | 87 | 16 | 12 | 43 | 3 | 12 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0003 | 0/0 | 2442 | 76 | 19 | 12 | 32 | 3 | 10 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0004 | 0/0 | 2442 | 63 | 7 | 23 | 22 | 3 | 8 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0005 | 0/0 | 2442 | 5 | 0 | 0 | 5 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0006 | 0/1 | 2442 | 4 | 0 | 0 | 2 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0007 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0008 | 0/0 | 2442 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0009 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0010 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0011 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0012 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0013 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0014 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0015 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0016 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0017 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0018 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| c0019 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0002 | 0/0 | 7 | 0 | 5 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0003 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0004 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0006 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0010 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2442 | 140 | 37 | 8 | 85 | 1 | 9 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0004 | 0/0 | 2442 | 63 | 7 | 23 | 22 | 3 | 8 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0007 | 0/0 | 2442 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0009 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0012 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0002 | 1/0 | 2442 | 87 | 16 | 12 | 43 | 3 | 12 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0003 | 0/0 | 2442 | 76 | 19 | 12 | 32 | 3 | 10 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0005 | 0/0 | 2442 | 5 | 0 | 0 | 5 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0014 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0015 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0018 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0019 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0003c0006 | 0/1 | 2442 | 4 | 0 | 0 | 2 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0004c0008 | 0/0 | 2442 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0005c0016 | 0/0 | 2442 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0006c0017 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0007c0013 | 0/0 | 2442 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0008c0011 | 0/0 | 2442 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0009c0010 | 0/0 | 2442 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3252 | 139 | 36 | 8 | 85 | 1 | 9 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0001t0002 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0004t0001 | 0/0 | 3252 | 63 | 7 | 23 | 22 | 3 | 8 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0007t0001 | 0/0 | 3252 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0009t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0001c0012t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0002t0001 | 1/0 | 3252 | 87 | 16 | 12 | 43 | 3 | 12 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0003t0001 | 0/0 | 3252 | 76 | 19 | 12 | 32 | 3 | 10 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0005t0001 | 0/0 | 3252 | 5 | 0 | 0 | 5 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0014t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0015t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0018t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0002c0019t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0003c0006t0001 | 0/1 | 3252 | 4 | 0 | 0 | 2 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0004c0008t0001 | 0/0 | 3252 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0005c0016t0001 | 0/0 | 3252 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0006c0017t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0007c0013t0001 | 0/0 | 3252 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0008c0011t0001 | 0/0 | 3252 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| a0009c0010t0001 | 0/0 | 3252 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | copy fasta | chr11 | 75581918 | 75674038 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0002 | 0/0 | 7 | 0 | 5 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0003 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0007t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0007t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0009t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0001c0012t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0010 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0004 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0005t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0014t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0015t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0018t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0002c0019t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0003c0006t0001g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0004c0008t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0004c0008t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0005c0016t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0006c0017t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0007c0013t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0008c0011t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| a0009c0010t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0003 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0245 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0131 | EUR | GBR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00280 | hp1 | a0005 | c0016 | t0001 | g0295 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0310 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | FIN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00408 | hp2 | a0009 | c0010 | t0001 | g0030 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0244 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0023 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0066 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0278 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0158 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00735 | hp2 | a0007 | c0013 | t0001 | g0063 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0132 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01069 | hp1 | a0001 | c0004 | t0001 | g0047 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0234 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0045 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01074 | hp1 | a0002 | c0019 | t0001 | g0336 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01074 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0048 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01167 | hp1 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0299 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0290 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01175 | hp1 | a0001 | c0004 | t0001 | g0097 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0156 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01192 | hp1 | a0001 | c0004 | t0001 | g0127 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0088 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01243 | hp1 | a0006 | c0017 | t0001 | g0309 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0057 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0003 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01258 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01346 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01346 | hp2 | a0002 | c0003 | t0001 | g0294 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0003 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0228 | EUR | IBS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0002 | EUR | IBS | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01928 | hp1 | a0002 | c0003 | t0001 | g0269 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0002 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0291 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0046 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0287 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0121 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02027 | hp1 | a0002 | c0015 | t0001 | g0241 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0122 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02055 | hp1 | a0001 | c0012 | t0001 | g0049 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02056 | hp1 | a0003 | c0006 | t0001 | g0187 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02071 | hp2 | a0004 | c0008 | t0001 | g0031 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0314 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02074 | hp2 | a0002 | c0018 | t0001 | g0237 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0311 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0014 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02129 | hp1 | a0001 | c0004 | t0001 | g0111 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0296 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02148 | hp1 | a0002 | c0003 | t0001 | g0301 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | CDX | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0305 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02273 | hp1 | a0002 | c0003 | t0001 | g0271 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0123 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0329 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0165 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0254 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02622 | hp1 | a0001 | c0004 | t0001 | g0069 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0316 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02717 | hp1 | a0001 | c0007 | t0001 | g0027 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0323 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0125 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0055 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0283 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0203 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02895 | hp1 | a0002 | c0003 | t0001 | g0282 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0304 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02922 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02965 | hp1 | a0002 | c0003 | t0001 | g0026 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0322 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0321 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03139 | hp1 | a0002 | c0003 | t0001 | g0025 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03225 | hp1 | a0001 | c0007 | t0001 | g0029 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03239 | hp1 | a0002 | c0003 | t0001 | g0292 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03453 | hp2 | a0002 | c0003 | t0001 | g0198 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0255 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0308 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03540 | hp1 | a0001 | c0009 | t0001 | g0028 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | GWD | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0199 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0293 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0230 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03669 | hp2 | a0002 | c0003 | t0001 | g0300 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0130 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0022 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0109 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0108 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03710 | hp2 | a0002 | c0003 | t0001 | g0022 | SAS | PJL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0024 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03834 | hp1 | a0002 | c0014 | t0001 | g0224 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0213 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0190 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0248 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04115 | hp1 | a0002 | c0003 | t0001 | g0289 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04115 | hp2 | a0001 | c0004 | t0001 | g0128 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0257 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04184 | hp2 | a0002 | c0003 | t0001 | g0319 | SAS | BEB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04199 | hp2 | a0002 | c0003 | t0001 | g0302 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0024 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0242 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0148 | SAS | STU | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0059 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18522 | hp2 | a0002 | c0003 | t0001 | g0330 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | CHB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0268 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0297 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18950 | hp1 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0113 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18952 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18953 | hp1 | a0001 | c0004 | t0001 | g0110 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0279 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18956 | hp2 | a0002 | c0005 | t0001 | g0335 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0281 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18962 | hp2 | a0002 | c0005 | t0001 | g0332 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18965 | hp1 | a0002 | c0003 | t0001 | g0251 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18965 | hp2 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18975 | hp1 | a0001 | c0004 | t0001 | g0120 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0014 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18977 | hp2 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18982 | hp2 | a0001 | c0004 | t0001 | g0089 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18984 | hp1 | a0002 | c0003 | t0001 | g0274 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0275 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18985 | hp2 | a0001 | c0004 | t0001 | g0112 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18987 | hp2 | a0001 | c0004 | t0001 | g0092 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18989 | hp1 | a0001 | c0004 | t0001 | g0116 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18989 | hp2 | a0004 | c0008 | t0001 | g0032 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0266 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18994 | hp2 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19005 | hp1 | a0002 | c0005 | t0001 | g0333 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0284 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0270 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0119 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19011 | hp2 | a0002 | c0005 | t0001 | g0334 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0324 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19043 | hp1 | a0002 | c0003 | t0001 | g0328 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0023 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19063 | hp2 | a0002 | c0005 | t0001 | g0331 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0288 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19072 | hp2 | a0002 | c0003 | t0001 | g0276 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19076 | hp1 | a0001 | c0004 | t0001 | g0095 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0277 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19078 | hp1 | a0003 | c0006 | t0001 | g0188 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19081 | hp1 | a0001 | c0004 | t0001 | g0114 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19082 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19084 | hp1 | a0001 | c0004 | t0001 | g0181 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19085 | hp2 | a0002 | c0003 | t0001 | g0261 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0280 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0272 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0157 | AFR | ASW | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20129 | hp2 | a0002 | c0003 | t0001 | g0317 | AFR | ASW | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20752 | hp1 | a0003 | c0006 | t0001 | g0115 | EUR | TSI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0318 | EUR | TSI | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20905 | hp1 | a0001 | c0004 | t0001 | g0160 | SAS | GIH | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | CLM | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02109 | hp2 | a0008 | c0011 | t0001 | g0155 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02559 | hp1 | a0002 | c0003 | t0001 | g0315 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | MSL | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0298 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | USA | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0210 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | LWK | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0006 | t0001 | g0189 | REF | REF | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0232 | REF | REF | MAP6_chr11_75581918_75674038 | MAP6 | chr11 | 75581918 | 75674038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75587108
|
A | G | 1 | a0006 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2393T>C | p.Val798Ala | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 3062/3252 | 2393/2442 | 798/813 | chr11 | 75587108 | ||
| chr11:75587282
|
C | T | 1 | a0008 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2219G>A | p.Arg740His | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2888/3252 | 2219/2442 | 740/813 | chr11 | 75587282 | ||
| chr11:75587423
|
A | C | 2 | a0003a0005 | 5 | HG00280.hp1 HG02056.hp1 NA19078.hp1 others(2): Show |
missense_variant | MODERATE | c.2078T>G | p.Val693Gly | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2747/3252 | 2078/2442 | 693/813 | chr11 | 75587423 | ||
| chr11:75587872
|
C | A | 1 | a0007 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1629G>T | p.Met543Ile | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2298/3252 | 1629/2442 | 543/813 | chr11 | 75587872 | ||
| chr11:75667629
|
A | C | 5 | a0001a0003a0004others(2): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
missense_variant | MODERATE | c.741T>G | p.Ile247Met | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1410/3252 | 741/2442 | 247/813 | chr11 | 75667629 | ||
| chr11:75667838
|
C | T | 1 | a0004 | 2 | HG02071.hp2 NA18989.hp2 |
missense_variant | MODERATE | c.532G>A | p.Val178Met | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1201/3252 | 532/2442 | 178/813 | chr11 | 75667838 | ||
| chr11:75667973
|
G | T | 1 | a0009 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.397C>A | p.Pro133Thr | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1066/3252 | 397/2442 | 133/813 | chr11 | 75667973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75587161
|
C | T | 2 | a0001c0012a0002c0019 | 2 | HG01074.hp1 HG02055.hp1 |
synonymous_variant | LOW | c.2340G>A | p.Lys780Lys | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 3009/3252 | 2340/2442 | 780/813 | chr11 | 75587161 | ||
| chr11:75587752
|
A | G | 6 | a0001c0004a0001c0009a0002c0003others(3): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
synonymous_variant | LOW | c.1749T>C | p.Asp583Asp | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2418/3252 | 1749/2442 | 583/813 | chr11 | 75587752 | ||
| chr11:75587971
|
C | T | 1 | a0002c0015 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.1530G>A | p.Thr510Thr | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 4/4 | 2199/3252 | 1530/2442 | 510/813 | chr11 | 75587971 | ||
| chr11:75605927
|
G | A | 1 | a0002c0018 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.1197C>T | p.Asp399Asp | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/4 | 1866/3252 | 1197/2442 | 399/813 | chr11 | 75605927 | ||
| chr11:75605942
|
C | T | 1 | a0002c0014 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.1182G>A | p.Thr394Thr | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/4 | 1851/3252 | 1182/2442 | 394/813 | chr11 | 75605942 | ||
| chr11:75667710
|
G | C | 1 | a0002c0005 | 5 | NA18956.hp2 NA18962.hp2 NA19005.hp1 others(2): Show |
synonymous_variant | LOW | c.660C>G | p.Gly220Gly | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1329/3252 | 660/2442 | 220/813 | chr11 | 75667710 | ||
| chr11:75667977
|
C | T | 2 | a0001c0007a0001c0009 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.393G>A | p.Gln131Gln | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 1062/3252 | 393/2442 | 131/813 | chr11 | 75667977 | ||
| chr11:75668190
|
G | A | 1 | a0002c0019 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.180C>T | p.Pro60Pro | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 849/3252 | 180/2442 | 60/813 | chr11 | 75668190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75668740
|
G | C | 1 | a0001c0001t0002 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-371C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/4 | 371 | chr11 | 75668740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:75588216
|
A | G | 1 | a0003c0006t0001g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1317-32T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588216 | ||||||
| chr11:75588381
|
C | T | 3 | a0002c0003t0001g0198a0002c0003t0001g0199a0002c0003t0001g0298 | 3 | HG03453.hp2 HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1317-197G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588381 | ||||||
| chr11:75588572
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1317-388C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588572 | ||||||
| chr11:75588902
|
C | T | 97 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0038others(94): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1317-718G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588902 | ||||||
| chr11:75588963
|
G | A | 1 | a0003c0006t0001g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1317-779C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588963 | ||||||
| chr11:75588963
|
G | T | 1 | a0002c0003t0001g0296 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1317-779C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588963 | ||||||
| chr11:75588988
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1317-804G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75588988 | ||||||
| chr11:75589003
|
G | A | 97 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(94): Show | 111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1317-819C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589003 | ||||||
| chr11:75589247
|
G | A | 3 | a0002c0003t0001g0294a0002c0003t0001g0301a0005c0016t0001g0295 | 3 | HG00280.hp1 HG01346.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1317-1063C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589247 | ||||||
| chr11:75589333
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1317-1149G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589333 | ||||||
| chr11:75589479
|
A | C | 1 | a0002c0002t0001g0206 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1317-1295T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589479 | ||||||
| chr11:75589552
|
G | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0104 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1317-1368C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589552 | ||||||
| chr11:75589622
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(260): Show | 302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1317-1438A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589622 | ||||||
| chr11:75589710
|
T | G | 8 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.1317-1526A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589710 | ||||||
| chr11:75589847
|
G | T | 1 | a0002c0003t0001g0280 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1317-1663C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75589847 | ||||||
| chr11:75590133
|
T | A | 1 | a0002c0002t0001g0257 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1317-1949A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590133 | ||||||
| chr11:75590234
|
G | A | 1 | a0002c0003t0001g0313 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1317-2050C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590234 | ||||||
| chr11:75590255
|
T | C | 6 | a0001c0001t0001g0077a0002c0002t0001g0218a0002c0002t0001g0222others(3): Show | 6 | NA18956.hp1 NA18986.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317-2071A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590255 | ||||||
| chr11:75590274
|
G | C | 1 | a0002c0002t0001g0257 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1317-2090C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590274 | ||||||
| chr11:75590462
|
G | A | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317-2278C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590462 | ||||||
| chr11:75590570
|
C | T | 1 | a0002c0003t0001g0296 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1317-2386G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590570 | ||||||
| chr11:75590613
|
T | A | 1 | a0001c0001t0002g0337 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1317-2429A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590613 | ||||||
| chr11:75590707
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0053a0001c0001t0001g0054 | 4 | HG02451.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317-2523G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590707 | ||||||
| chr11:75590970
|
GA | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(103): Show | 127 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.1317-2787delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75590970 | ||||||
| chr11:75591022
|
G | A | 3 | a0001c0001t0001g0103a0001c0012t0001g0049a0002c0019t0001g0336 | 3 | HG01074.hp1 HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1317-2838C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591022 | ||||||
| chr11:75591103
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0060 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1317-2919G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591103 | ||||||
| chr11:75591219
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1317-3035T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591219 | ||||||
| chr11:75591230
|
A | G | 27 | a0001c0004t0001g0041a0002c0003t0001g0022a0002c0003t0001g0023others(24): Show | 30 | HG00597.hp1 HG00621.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1317-3046T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591230 | ||||||
| chr11:75591330
|
T | G | 1 | a0002c0002t0001g0212 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1317-3146A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591330 | ||||||
| chr11:75591375
|
T | C | 5 | a0002c0003t0001g0294a0002c0003t0001g0300a0002c0003t0001g0301others(2): Show | 5 | HG00280.hp1 HG01346.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1317-3191A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591375 | ||||||
| chr11:75591380
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1317-3196A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591380 | ||||||
| chr11:75591523
|
C | G | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317-3339G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591523 | ||||||
| chr11:75591657
|
A | G | 3 | a0002c0002t0001g0247a0002c0002t0001g0248a0002c0014t0001g0224 | 3 | HG03831.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1317-3473T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591657 | ||||||
| chr11:75591681
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0103a0001c0001t0001g0192others(5): Show | 10 | HG01074.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1317-3497G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591681 | ||||||
| chr11:75591710
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1317-3526C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591710 | ||||||
| chr11:75591810
|
A | G | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(268): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1317-3626T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75591810 | ||||||
| chr11:75592181
|
G | C | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1317-3997C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592181 | ||||||
| chr11:75592222
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(153): Show | 183 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1317-4038A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592222 | ||||||
| chr11:75592238
|
G | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18946.hp2 NA18964.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1317-4054C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592238 | ||||||
| chr11:75592313
|
C | T | 2 | a0002c0002t0001g0007a0002c0002t0001g0223 | 4 | NA18942.hp2 NA18945.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1317-4129G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592313 | ||||||
| chr11:75592394
|
A | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(260): Show | 302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1317-4210T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592394 | ||||||
| chr11:75592500
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1317-4316G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592500 | ||||||
| chr11:75592578
|
C | G | 2 | a0001c0001t0001g0075a0001c0001t0001g0082 | 2 | NA18957.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1317-4394G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592578 | ||||||
| chr11:75592579
|
C | T | 2 | a0001c0004t0001g0034a0001c0004t0001g0035 | 2 | HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1317-4395G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592579 | ||||||
| chr11:75592629
|
G | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(259): Show | 301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1317-4445C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592629 | ||||||
| chr11:75592680
|
A | C | 1 | a0002c0002t0001g0260 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1317-4496T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592680 | ||||||
| chr11:75592897
|
G | A | 2 | a0001c0001t0001g0078a0002c0002t0001g0273 | 2 | HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1317-4713C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592897 | ||||||
| chr11:75592949
|
G | A | 1 | a0002c0002t0001g0202 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1317-4765C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75592949 | ||||||
| chr11:75593047
|
C | G | 1 | a0001c0001t0001g0018 | 2 | NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1317-4863G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593047 | ||||||
| chr11:75593048
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317-4864T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593048 | ||||||
| chr11:75593306
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1317-5122A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593306 | ||||||
| chr11:75593497
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317-5313T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593497 | ||||||
| chr11:75593601
|
T | C | 1 | a0002c0002t0001g0205 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1317-5417A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593601 | ||||||
| chr11:75593655
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1317-5471C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593655 | ||||||
| chr11:75593786
|
C | T | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0082others(1): Show | 4 | HG01975.hp1 NA18957.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1317-5602G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593786 | ||||||
| chr11:75593787
|
G | A | 1 | a0002c0003t0001g0323 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1317-5603C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593787 | ||||||
| chr11:75593864
|
A | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0103a0001c0001t0001g0192others(6): Show | 11 | HG01074.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1317-5680T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593864 | ||||||
| chr11:75593954
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(267): Show | 311 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.1317-5770G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593954 | ||||||
| chr11:75593970
|
A | T | 21 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028others(18): Show | 22 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(19): Show |
intron_variant | MODIFIER | c.1317-5786T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593970 | ||||||
| chr11:75593986
|
GA | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(125): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1317-5803delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75593986 | ||||||
| chr11:75594062
|
C | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(15): Show | 29 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1317-5878G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594062 | ||||||
| chr11:75594342
|
T | C | 2 | a0002c0002t0001g0020a0002c0002t0001g0260 | 3 | HG01123.hp1 HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1317-6158A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594342 | ||||||
| chr11:75594363
|
C | T | 1 | a0002c0003t0001g0282 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1317-6179G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594363 | ||||||
| chr11:75594486
|
C | T | 48 | a0001c0004t0001g0055a0001c0007t0001g0027a0001c0007t0001g0029others(45): Show | 54 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1317-6302G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594486 | ||||||
| chr11:75594512
|
G | A | 80 | a0001c0004t0001g0041a0001c0004t0001g0055a0001c0004t0001g0059others(77): Show | 89 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.1317-6328C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594512 | ||||||
| chr11:75594820
|
G | A | 48 | a0001c0004t0001g0055a0001c0007t0001g0027a0001c0007t0001g0029others(45): Show | 54 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1317-6636C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594820 | ||||||
| chr11:75594931
|
G | A | 1 | a0001c0004t0001g0046 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1317-6747C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75594931 | ||||||
| chr11:75595172
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(258): Show | 300 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1317-6988G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595172 | ||||||
| chr11:75595184
|
C | T | 1 | a0002c0003t0001g0316 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1317-7000G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595184 | ||||||
| chr11:75595245
|
C | G | 1 | a0001c0001t0001g0178 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1317-7061G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595245 | ||||||
| chr11:75595437
|
C | A | 2 | a0002c0002t0001g0306a0002c0002t0001g0307 | 2 | NA18941.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1317-7253G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595437 | ||||||
| chr11:75595640
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1317-7456G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595640 | ||||||
| chr11:75595702
|
T | C | 20 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(17): Show | 20 | HG02056.hp1 HG02109.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1317-7518A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595702 | ||||||
| chr11:75595934
|
G | T | 129 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(126): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1317-7750C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75595934 | ||||||
| chr11:75596253
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(269): Show | 313 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1317-8069G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596253 | ||||||
| chr11:75596318
|
T | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(264): Show | 308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.1317-8134A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596318 | ||||||
| chr11:75596354
|
T | G | 23 | a0002c0003t0001g0022a0002c0003t0001g0023a0002c0003t0001g0240others(20): Show | 25 | HG00597.hp1 HG00621.hp1 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.1317-8170A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596354 | ||||||
| chr11:75596375
|
C | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 43 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1317-8191G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596375 | ||||||
| chr11:75596481
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1317-8297T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596481 | ||||||
| chr11:75596559
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(169): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1317-8375C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596559 | ||||||
| chr11:75596775
|
C | T | 129 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(126): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1317-8591G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596775 | ||||||
| chr11:75596814
|
T | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(260): Show | 302 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1317-8630A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596814 | ||||||
| chr11:75596831
|
G | C | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1317-8647C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596831 | ||||||
| chr11:75596872
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1317-8688C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596872 | ||||||
| chr11:75596886
|
G | A | 129 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(126): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1317-8702C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596886 | ||||||
| chr11:75596953
|
T | A | 30 | a0001c0004t0001g0041a0002c0003t0001g0022a0002c0003t0001g0023others(27): Show | 33 | HG00597.hp1 HG00621.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1317-8769A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75596953 | ||||||
| chr11:75597072
|
C | T | 1 | a0002c0003t0001g0240 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1316+8736G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597072 | ||||||
| chr11:75597128
|
C | T | 129 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(126): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1316+8680G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597128 | ||||||
| chr11:75597138
|
A | T | 52 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(49): Show | 65 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1316+8670T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597138 | ||||||
| chr11:75597272
|
T | G | 2 | a0002c0003t0001g0240a0002c0003t0001g0261 | 2 | NA19063.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1316+8536A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597272 | ||||||
| chr11:75597402
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(257): Show | 299 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1316+8406C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597402 | ||||||
| chr11:75597602
|
C | T | 6 | a0002c0003t0001g0004a0002c0003t0001g0275a0002c0003t0001g0279others(3): Show | 10 | HG00738.hp2 HG01081.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1316+8206G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597602 | ||||||
| chr11:75597646
|
T | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0060 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1316+8162A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597646 | ||||||
| chr11:75597717
|
A | G | 2 | a0002c0003t0001g0026a0002c0003t0001g0315 | 3 | HG02559.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1316+8091T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75597717 | ||||||
| chr11:75598100
|
A | G | 262 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(259): Show | 301 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1316+7708T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598100 | ||||||
| chr11:75598179
|
C | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0179 | 2 | NA18970.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1316+7629G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598179 | ||||||
| chr11:75598241
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1316+7567G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598241 | ||||||
| chr11:75598291
|
G | C | 1 | a0001c0004t0001g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1316+7517C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598291 | ||||||
| chr11:75598526
|
T | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(258): Show | 300 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1316+7282A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598526 | ||||||
| chr11:75598675
|
A | T | 1 | a0003c0006t0001g0188 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1316+7133T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75598675 | ||||||
| chr11:75599092
|
C | T | 1 | a0001c0004t0001g0088 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1316+6716G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599092 | ||||||
| chr11:75599250
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1316+6558A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599250 | ||||||
| chr11:75599703
|
T | C | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1316+6105A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599703 | ||||||
| chr11:75599710
|
G | A | 1 | a0002c0003t0001g0323 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1316+6098C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599710 | ||||||
| chr11:75599782
|
G | T | 31 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 43 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1316+6026C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599782 | ||||||
| chr11:75599878
|
C | T | 1 | a0002c0003t0001g0304 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1316+5930G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75599878 | ||||||
| chr11:75600034
|
T | C | 4 | a0002c0002t0001g0204a0002c0002t0001g0209a0002c0002t0001g0211others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1316+5774A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600034 | ||||||
| chr11:75600056
|
T | A | 1 | a0001c0004t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1316+5752A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600056 | ||||||
| chr11:75600155
|
G | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(7): Show | 10 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1316+5653C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600155 | ||||||
| chr11:75600398
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | NA18957.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1316+5410T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600398 | ||||||
| chr11:75600635
|
A | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(7): Show | 10 | HG02622.hp1 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1316+5173T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600635 | ||||||
| chr11:75600650
|
G | A | 2 | a0002c0002t0001g0247a0002c0002t0001g0248 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1316+5158C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600650 | ||||||
| chr11:75600659
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(182): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1316+5149A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75600659 | ||||||
| chr11:75601114
|
A | G | 1 | a0002c0003t0001g0289 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1316+4694T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601114 | ||||||
| chr11:75601381
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+4427A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601381 | ||||||
| chr11:75601502
|
C | T | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1316+4306G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601502 | ||||||
| chr11:75601619
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1316+4189G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601619 | ||||||
| chr11:75601741
|
G | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+4067C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601741 | ||||||
| chr11:75601858
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1316+3950A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601858 | ||||||
| chr11:75601965
|
G | A | 2 | a0002c0002t0001g0021a0002c0002t0001g0264 | 3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1316+3843C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601965 | ||||||
| chr11:75601986
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1316+3822G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75601986 | ||||||
| chr11:75602045
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+3763A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602045 | ||||||
| chr11:75602328
|
G | T | 1 | a0002c0003t0001g0267 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1316+3480C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602328 | ||||||
| chr11:75602346
|
T | C | 5 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035others(2): Show | 6 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316+3462A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602346 | ||||||
| chr11:75602972
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1316+2836A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75602972 | ||||||
| chr11:75603077
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(25): Show | 40 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1316+2731C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603077 | ||||||
| chr11:75603211
|
C | T | 5 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035others(2): Show | 6 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316+2597G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603211 | ||||||
| chr11:75603251
|
G | A | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316+2557C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603251 | ||||||
| chr11:75603549
|
C | T | 2 | a0001c0004t0001g0059a0001c0004t0001g0069 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1316+2259G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603549 | ||||||
| chr11:75603741
|
C | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+2067G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603741 | ||||||
| chr11:75603742
|
G | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(169): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1316+2066C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603742 | ||||||
| chr11:75603743
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(169): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1316+2065G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603743 | ||||||
| chr11:75603924
|
C | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+1884G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75603924 | ||||||
| chr11:75604017
|
A | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+1791T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604017 | ||||||
| chr11:75604071
|
C | A | 1 | a0001c0007t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1316+1737G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604071 | ||||||
| chr11:75604126
|
T | C | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+1682A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604126 | ||||||
| chr11:75604458
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1316+1350C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604458 | ||||||
| chr11:75604501
|
G | GT | 31 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(28): Show | 43 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1316+1306_1316+130 others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604501 | ||||||
| chr11:75604507
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1316+1301C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604507 | ||||||
| chr11:75604597
|
G | GT | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316+1210dupA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604597 | ||||||
| chr11:75604597
|
GT | G | 9 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0074others(6): Show | 9 | HG00558.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1316+1210delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604597 | ||||||
| chr11:75604598
|
T | A | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1316+1210A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604598 | ||||||
| chr11:75604687
|
C | CCA | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1316+1119_1316+112 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604687 | ||||||
| chr11:75604744
|
C | T | 1 | a0007c0013t0001g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1316+1064G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604744 | ||||||
| chr11:75604830
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1316+978G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604830 | ||||||
| chr11:75604985
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1316+823A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604985 | ||||||
| chr11:75604997
|
C | T | 1 | a0002c0003t0001g0275 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1316+811G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75604997 | ||||||
| chr11:75605004
|
C | T | 1 | a0002c0002t0001g0235 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1316+804G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605004 | ||||||
| chr11:75605133
|
C | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1316+675G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605133 | ||||||
| chr11:75605154
|
G | A | 2 | a0001c0001t0001g0078a0002c0002t0001g0273 | 2 | HG01433.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1316+654C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605154 | ||||||
| chr11:75605155
|
T | C | 1 | a0002c0003t0001g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1316+653A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605155 | ||||||
| chr11:75605486
|
C | T | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1316+322G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605486 | ||||||
| chr11:75605487
|
G | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1316+321C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605487 | ||||||
| chr11:75605501
|
G | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1316+307C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605501 | ||||||
| chr11:75605549
|
A | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 7 | HG02622.hp2 HG02809.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+259T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605549 | ||||||
| chr11:75605554
|
A | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0149a0001c0001t0001g0150others(4): Show | 7 | HG02622.hp2 HG02809.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1316+254T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 3/3 | chr11 | 75605554 | ||||||
| chr11:75606128
|
G | A | 11 | a0001c0001t0001g0043a0001c0001t0001g0050a0001c0001t0001g0058others(8): Show | 11 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1120-124C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606128 | ||||||
| chr11:75606227
|
T | G | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120-223A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606227 | ||||||
| chr11:75606332
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1120-328C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606332 | ||||||
| chr11:75606418
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(179): Show | 212 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1120-414A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606418 | ||||||
| chr11:75606557
|
C | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.1120-553G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606557 | ||||||
| chr11:75606717
|
A | G | 186 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(183): Show | 216 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1120-713T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606717 | ||||||
| chr11:75606777
|
A | T | 271 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(268): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1120-773T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606777 | ||||||
| chr11:75606997
|
G | A | 1 | a0002c0002t0001g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1120-993C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75606997 | ||||||
| chr11:75607252
|
G | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 52 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1119+857C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607252 | ||||||
| chr11:75607392
|
T | C | 1 | a0002c0003t0001g0310 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1119+717A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607392 | ||||||
| chr11:75607574
|
T | C | 5 | a0002c0002t0001g0312a0002c0002t0001g0320a0002c0002t0001g0321others(2): Show | 5 | HG02451.hp2 HG02723.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+535A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607574 | ||||||
| chr11:75607619
|
G | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1119+490C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607619 | ||||||
| chr11:75607619
|
GAGA | G | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1119+487_1119+489d others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607619 | ||||||
| chr11:75607733
|
G | A | 29 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(26): Show | 41 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1119+376C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 2/3 | chr11 | 75607733 | ||||||
| chr11:75608344
|
T | C | 1 | a0002c0018t0001g0237 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.906-22A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75608344 | ||||||
| chr11:75608737
|
T | C | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-415A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75608737 | ||||||
| chr11:75608923
|
G | A | 1 | a0004c0008t0001g0031 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.906-601C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75608923 | ||||||
| chr11:75609032
|
G | A | 8 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(5): Show | 8 | HG02622.hp2 HG02809.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.906-710C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609032 | ||||||
| chr11:75609060
|
C | T | 5 | a0002c0003t0001g0294a0002c0003t0001g0300a0002c0003t0001g0301others(2): Show | 5 | HG00280.hp1 HG01346.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-738G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609060 | ||||||
| chr11:75609161
|
T | A | 7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.906-839A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609161 | ||||||
| chr11:75609330
|
C | A | 1 | a0002c0002t0001g0219 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.906-1008G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609330 | ||||||
| chr11:75609366
|
G | C | 2 | a0001c0004t0001g0059a0001c0004t0001g0069 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.906-1044C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609366 | ||||||
| chr11:75609434
|
G | A | 254 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(251): Show | 293 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.906-1112C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609434 | ||||||
| chr11:75609452
|
C | T | 249 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(246): Show | 288 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.906-1130G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609452 | ||||||
| chr11:75609552
|
C | T | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(4): Show | 7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-1230G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609552 | ||||||
| chr11:75609623
|
C | T | 75 | a0001c0004t0001g0041a0002c0002t0001g0286a0002c0002t0001g0308others(72): Show | 84 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.906-1301G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609623 | ||||||
| chr11:75609806
|
G | T | 1 | a0001c0001t0001g0018 | 2 | NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.906-1484C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609806 | ||||||
| chr11:75609846
|
G | T | 1 | a0002c0002t0001g0303 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.906-1524C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75609846 | ||||||
| chr11:75610339
|
A | T | 1 | a0002c0002t0001g0325 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.906-2017T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610339 | ||||||
| chr11:75610765
|
G | C | 1 | a0007c0013t0001g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.906-2443C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610765 | ||||||
| chr11:75610832
|
C | T | 2 | a0002c0003t0001g0290a0002c0003t0001g0299 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.906-2510G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610832 | ||||||
| chr11:75610843
|
T | C | 1 | a0002c0014t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.906-2521A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610843 | ||||||
| chr11:75610917
|
T | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0044others(20): Show | 25 | HG00558.hp1 HG00597.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.906-2595A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75610917 | ||||||
| chr11:75611162
|
G | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(4): Show | 7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-2840C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611162 | ||||||
| chr11:75611187
|
C | G | 2 | a0002c0002t0001g0021a0002c0002t0001g0264 | 3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.906-2865G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611187 | ||||||
| chr11:75611546
|
C | T | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(4): Show | 7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-3224G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611546 | ||||||
| chr11:75611574
|
A | T | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(4): Show | 7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-3252T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611574 | ||||||
| chr11:75611628
|
A | C | 1 | a0001c0004t0001g0181 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.906-3306T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611628 | ||||||
| chr11:75611787
|
C | T | 1 | a0002c0003t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.906-3465G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611787 | ||||||
| chr11:75611793
|
T | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(4): Show | 7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-3471A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611793 | ||||||
| chr11:75611923
|
A | G | 1 | a0002c0003t0001g0210 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.906-3601T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611923 | ||||||
| chr11:75611958
|
C | T | 2 | a0002c0002t0001g0021a0002c0002t0001g0264 | 3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.906-3636G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611958 | ||||||
| chr11:75611995
|
G | A | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-3673C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75611995 | ||||||
| chr11:75612204
|
C | G | 1 | a0002c0003t0001g0282 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.906-3882G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612204 | ||||||
| chr11:75612338
|
G | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0104others(1): Show | 4 | HG02976.hp2 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-4016C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612338 | ||||||
| chr11:75612596
|
C | G | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(4): Show | 7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-4274G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612596 | ||||||
| chr11:75612755
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-4433G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75612755 | ||||||
| chr11:75613067
|
T | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0149others(4): Show | 7 | HG02809.hp1 HG03209.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-4745A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613067 | ||||||
| chr11:75613135
|
C | T | 75 | a0002c0002t0001g0286a0002c0002t0001g0303a0002c0002t0001g0308others(72): Show | 84 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.906-4813G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613135 | ||||||
| chr11:75613353
|
C | T | 2 | a0001c0004t0001g0059a0001c0004t0001g0069 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.906-5031G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613353 | ||||||
| chr11:75613442
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.906-5120C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613442 | ||||||
| chr11:75613499
|
C | T | 70 | a0001c0001t0001g0036a0001c0001t0001g0043a0001c0001t0001g0050others(67): Show | 74 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.906-5177G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613499 | ||||||
| chr11:75613554
|
G | A | 41 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0058others(38): Show | 43 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.906-5232C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613554 | ||||||
| chr11:75613564
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.906-5242C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613564 | ||||||
| chr11:75613703
|
T | A | 2 | a0001c0001t0001g0042a0001c0004t0001g0041 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.906-5381A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613703 | ||||||
| chr11:75613704
|
C | G | 2 | a0001c0001t0001g0042a0001c0004t0001g0041 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.906-5382G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613704 | ||||||
| chr11:75613733
|
A | G | 263 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(260): Show | 298 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.906-5411T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613733 | ||||||
| chr11:75613837
|
C | T | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-5515G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75613837 | ||||||
| chr11:75614057
|
C | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 5 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-5735G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614057 | ||||||
| chr11:75614139
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(203): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.906-5817A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614139 | ||||||
| chr11:75614241
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0050others(9): Show | 12 | HG00280.hp2 HG00639.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.906-5919G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614241 | ||||||
| chr11:75614354
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.906-6032G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614354 | ||||||
| chr11:75614524
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.906-6202G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614524 | ||||||
| chr11:75614545
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.906-6223G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75614545 | ||||||
| chr11:75615120
|
G | A | 6 | a0001c0001t0001g0062a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-6798C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615120 | ||||||
| chr11:75615223
|
T | G | 1 | a0001c0001t0001g0087 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.906-6901A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615223 | ||||||
| chr11:75615312
|
T | C | 1 | a0002c0002t0001g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.906-6990A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615312 | ||||||
| chr11:75615328
|
G | A | 2 | a0001c0001t0001g0105a0002c0003t0001g0284 | 2 | HG02129.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.906-7006C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615328 | ||||||
| chr11:75615418
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-7096C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615418 | ||||||
| chr11:75615541
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.906-7219G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615541 | ||||||
| chr11:75615578
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0192others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-7256G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615578 | ||||||
| chr11:75615626
|
G | C | 19 | a0002c0002t0001g0312a0002c0002t0001g0320a0002c0002t0001g0321others(16): Show | 20 | HG00323.hp1 HG00639.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.906-7304C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615626 | ||||||
| chr11:75615686
|
C | A | 6 | a0001c0001t0001g0062a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-7364G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615686 | ||||||
| chr11:75615691
|
G | C | 74 | a0001c0001t0001g0146a0002c0002t0001g0286a0002c0002t0001g0303others(71): Show | 83 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.906-7369C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615691 | ||||||
| chr11:75615967
|
C | T | 1 | a0002c0002t0001g0250 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.906-7645G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75615967 | ||||||
| chr11:75616029
|
T | C | 1 | a0002c0003t0001g0281 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.906-7707A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616029 | ||||||
| chr11:75616307
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-7985G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616307 | ||||||
| chr11:75616404
|
T | C | 3 | a0002c0003t0001g0282a0002c0003t0001g0283a0002c0003t0001g0305 | 3 | HG02257.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.906-8082A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616404 | ||||||
| chr11:75616425
|
A | G | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-8103T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616425 | ||||||
| chr11:75616667
|
G | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0044others(33): Show | 40 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.906-8345C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616667 | ||||||
| chr11:75616829
|
A | G | 1 | a0001c0004t0001g0156 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.906-8507T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616829 | ||||||
| chr11:75616845
|
G | A | 4 | a0001c0001t0001g0071a0001c0001t0001g0079a0001c0001t0001g0081others(1): Show | 4 | NA18981.hp1 NA19003.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-8523C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616845 | ||||||
| chr11:75616975
|
A | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0176a0001c0001t0001g0180 | 3 | NA18964.hp2 NA18993.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.906-8653T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75616975 | ||||||
| chr11:75617342
|
C | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(1): Show | 5 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-9020G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617342 | ||||||
| chr11:75617514
|
C | CA | 116 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0040others(113): Show | 130 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.906-9193dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | ||||||
| chr11:75617514
|
C | CAA | 20 | a0001c0001t0001g0038a0001c0004t0001g0035a0002c0002t0001g0242others(17): Show | 20 | HG01167.hp2 HG01346.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.906-9194_906-9193d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | ||||||
| chr11:75617514
|
CA | C | 10 | a0001c0001t0001g0192a0001c0004t0001g0048a0001c0007t0001g0027others(7): Show | 10 | HG01099.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.906-9193delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | ||||||
| chr11:75617514
|
CAA | C | 11 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0037others(8): Show | 13 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.906-9194_906-9193d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | ||||||
| chr11:75617514
|
CAAA | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(22): Show | 36 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.906-9195_906-9193d others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617514 | ||||||
| chr11:75617519
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-9197T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617519 | ||||||
| chr11:75617802
|
G | A | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-9480C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75617802 | ||||||
| chr11:75618107
|
CT | C | 268 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(265): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.906-9786delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618107 | ||||||
| chr11:75618107
|
CTT | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(44): Show | 59 | HG00280.hp1 HG00558.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.906-9787_906-9786d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618107 | ||||||
| chr11:75618245
|
C | A | 1 | a0002c0002t0001g0248 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.906-9923G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618245 | ||||||
| chr11:75618376
|
G | A | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-10054C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618376 | ||||||
| chr11:75618396
|
C | T | 9 | a0002c0003t0001g0310a0002c0003t0001g0311a0002c0003t0001g0313others(6): Show | 9 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-10074G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618396 | ||||||
| chr11:75618489
|
C | A | 1 | a0002c0002t0001g0303 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.906-10167G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618489 | ||||||
| chr11:75618599
|
TA | T | 13 | a0001c0001t0001g0136a0001c0001t0001g0146a0001c0001t0001g0184others(10): Show | 13 | HG01099.hp2 HG02056.hp1 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.906-10278delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618599 | ||||||
| chr11:75618692
|
G | A | 2 | a0001c0004t0001g0113a0001c0004t0001g0120 | 2 | NA18950.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.906-10370C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618692 | ||||||
| chr11:75618744
|
T | C | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-10422A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618744 | ||||||
| chr11:75618771
|
A | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.906-10449T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618771 | ||||||
| chr11:75618800
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.906-10478C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618800 | ||||||
| chr11:75618803
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-10481C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618803 | ||||||
| chr11:75618890
|
C | G | 2 | a0002c0002t0001g0221a0002c0002t0001g0228 | 2 | HG01258.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.906-10568G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618890 | ||||||
| chr11:75618923
|
G | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-10601C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618923 | ||||||
| chr11:75618976
|
G | T | 4 | a0002c0003t0001g0265a0002c0003t0001g0266a0002c0003t0001g0268others(1): Show | 4 | NA18942.hp1 NA18975.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-10654C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618976 | ||||||
| chr11:75618998
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0193a0001c0001t0001g0195 | 4 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-10676C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75618998 | ||||||
| chr11:75619098
|
T | G | 1 | a0002c0005t0001g0335 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.906-10776A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619098 | ||||||
| chr11:75619152
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 48 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.906-10830C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619152 | ||||||
| chr11:75619307
|
C | T | 5 | a0002c0002t0001g0306a0002c0002t0001g0307a0002c0003t0001g0004others(2): Show | 9 | HG00738.hp2 HG01081.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.906-10985G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619307 | ||||||
| chr11:75619308
|
A | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-10986T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619308 | ||||||
| chr11:75619380
|
TTTTTAAC | T | 9 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(6): Show | 9 | HG02056.hp1 HG02717.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-11065_906-1105 others(11): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619380 | ||||||
| chr11:75619453
|
C | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0192others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-11131G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619453 | ||||||
| chr11:75619507
|
C | T | 4 | a0002c0002t0001g0303a0002c0003t0001g0298a0002c0003t0001g0317others(1): Show | 4 | HG02970.hp2 HG06807.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-11185G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619507 | ||||||
| chr11:75619662
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-11340G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619662 | ||||||
| chr11:75619757
|
T | C | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0096 | 3 | NA18972.hp2 NA18991.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.906-11435A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75619757 | ||||||
| chr11:75620176
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-11854A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620176 | ||||||
| chr11:75620235
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(33): Show | 48 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.906-11913G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620235 | ||||||
| chr11:75620278
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0068 | 2 | HG02895.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.906-11956G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620278 | ||||||
| chr11:75620326
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-12004G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620326 | ||||||
| chr11:75620483
|
G | GA | 41 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 54 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.906-12162dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620483 | ||||||
| chr11:75620483
|
GA | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0037others(8): Show | 12 | HG01515.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.906-12162delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620483 | ||||||
| chr11:75620514
|
G | T | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-12192C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620514 | ||||||
| chr11:75620522
|
A | C | 5 | a0001c0004t0001g0045a0001c0004t0001g0046a0001c0004t0001g0047others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.906-12200T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620522 | ||||||
| chr11:75620543
|
A | G | 1 | a0001c0001t0002g0337 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.906-12221T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620543 | ||||||
| chr11:75620709
|
C | T | 4 | a0002c0002t0001g0303a0002c0003t0001g0298a0002c0003t0001g0317others(1): Show | 4 | HG02970.hp2 HG06807.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-12387G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620709 | ||||||
| chr11:75620902
|
G | A | 1 | a0002c0014t0001g0224 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.906-12580C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620902 | ||||||
| chr11:75620987
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.906-12665G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620987 | ||||||
| chr11:75620992
|
G | A | 1 | a0002c0003t0001g0304 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.906-12670C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620992 | ||||||
| chr11:75620997
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-12675C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75620997 | ||||||
| chr11:75621060
|
G | A | 1 | a0001c0004t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.906-12738C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621060 | ||||||
| chr11:75621304
|
T | A | 2 | a0002c0003t0001g0304a0006c0017t0001g0309 | 2 | HG01243.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.906-12982A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621304 | ||||||
| chr11:75621315
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-12993T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621315 | ||||||
| chr11:75621515
|
C | T | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-13193G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621515 | ||||||
| chr11:75621595
|
T | C | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-13273A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621595 | ||||||
| chr11:75621702
|
C | CA | 336 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(333): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.906-13381dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621702 | ||||||
| chr11:75621720
|
A | C | 1 | a0001c0004t0001g0110 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.906-13398T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75621720 | ||||||
| chr11:75622060
|
A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | NA18955.hp1 NA18968.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-13738T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622060 | ||||||
| chr11:75622108
|
G | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0192others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-13786C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622108 | ||||||
| chr11:75622236
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-13914C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622236 | ||||||
| chr11:75622320
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.906-13998A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622320 | ||||||
| chr11:75622394
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-14072C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622394 | ||||||
| chr11:75622431
|
AGTGCAAT others(4): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-14120_906-1411 others(15): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622431 | ||||||
| chr11:75622529
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-14207C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622529 | ||||||
| chr11:75622549
|
A | G | 5 | a0002c0002t0001g0306a0002c0002t0001g0307a0002c0003t0001g0004others(2): Show | 9 | HG00738.hp2 HG01081.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.906-14227T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622549 | ||||||
| chr11:75622740
|
C | T | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-14418G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622740 | ||||||
| chr11:75622977
|
T | C | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-14655A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75622977 | ||||||
| chr11:75623023
|
A | G | 1 | a0002c0002t0001g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.906-14701T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623023 | ||||||
| chr11:75623096
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-14774A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623096 | ||||||
| chr11:75623119
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.906-14797A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623119 | ||||||
| chr11:75623331
|
G | A | 3 | a0002c0003t0001g0026a0002c0003t0001g0315a0002c0003t0001g0316 | 4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-15009C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623331 | ||||||
| chr11:75623364
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-15042G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623364 | ||||||
| chr11:75623697
|
C | T | 1 | a0002c0002t0001g0231 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.906-15375G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623697 | ||||||
| chr11:75623735
|
A | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0192others(3): Show | 7 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-15413T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623735 | ||||||
| chr11:75623740
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.906-15418G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623740 | ||||||
| chr11:75623771
|
G | A | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.906-15449C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623771 | ||||||
| chr11:75623802
|
C | T | 2 | a0002c0002t0001g0312a0002c0002t0001g0320 | 2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.906-15480G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623802 | ||||||
| chr11:75623936
|
C | T | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-15614G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75623936 | ||||||
| chr11:75624455
|
C | T | 1 | a0001c0004t0001g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.906-16133G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624455 | ||||||
| chr11:75624754
|
C | T | 70 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(67): Show | 83 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.906-16432G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624754 | ||||||
| chr11:75624760
|
G | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-16438C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624760 | ||||||
| chr11:75624776
|
A | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0037a0001c0001t0001g0192others(3): Show | 7 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.906-16454T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75624776 | ||||||
| chr11:75625009
|
C | A | 1 | a0002c0003t0001g0301 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.906-16687G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625009 | ||||||
| chr11:75625211
|
G | A | 1 | a0002c0002t0001g0249 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.906-16889C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625211 | ||||||
| chr11:75625226
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-16904A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625226 | ||||||
| chr11:75625364
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.906-17042T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625364 | ||||||
| chr11:75625443
|
A | G | 1 | a0007c0013t0001g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.906-17121T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625443 | ||||||
| chr11:75625559
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.906-17237T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625559 | ||||||
| chr11:75625578
|
A | C | 1 | a0003c0006t0001g0188 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906-17256T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625578 | ||||||
| chr11:75625667
|
C | A | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-17345G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625667 | ||||||
| chr11:75625708
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-17386T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625708 | ||||||
| chr11:75625885
|
C | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0044a0001c0001t0001g0072others(7): Show | 11 | HG00597.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.906-17563G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75625885 | ||||||
| chr11:75626158
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-17836G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626158 | ||||||
| chr11:75626190
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.906-17868G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626190 | ||||||
| chr11:75626481
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-18159T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626481 | ||||||
| chr11:75626499
|
G | A | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-18177C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626499 | ||||||
| chr11:75626507
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.906-18185C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626507 | ||||||
| chr11:75626689
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-18367G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626689 | ||||||
| chr11:75626863
|
G | A | 1 | a0002c0002t0001g0273 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.906-18541C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626863 | ||||||
| chr11:75626872
|
A | G | 8 | a0001c0001t0001g0154a0001c0004t0001g0014a0001c0004t0001g0111others(5): Show | 9 | HG02027.hp2 HG02083.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-18550T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626872 | ||||||
| chr11:75626904
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-18582A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626904 | ||||||
| chr11:75626962
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-18640T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75626962 | ||||||
| chr11:75627046
|
T | C | 1 | a0002c0003t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.906-18724A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627046 | ||||||
| chr11:75627159
|
G | C | 1 | a0003c0006t0001g0187 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.906-18837C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627159 | ||||||
| chr11:75627214
|
G | T | 1 | a0001c0004t0001g0110 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.906-18892C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627214 | ||||||
| chr11:75627423
|
C | T | 1 | a0002c0002t0001g0230 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.906-19101G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627423 | ||||||
| chr11:75627424
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-19102C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627424 | ||||||
| chr11:75627697
|
T | G | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-19375A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627697 | ||||||
| chr11:75627730
|
G | A | 1 | a0002c0003t0001g0311 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.906-19408C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627730 | ||||||
| chr11:75627852
|
T | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0037others(6): Show | 10 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.906-19530A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627852 | ||||||
| chr11:75627953
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-19631A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627953 | ||||||
| chr11:75627972
|
C | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.906-19650G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75627972 | ||||||
| chr11:75628029
|
C | T | 3 | a0002c0003t0001g0328a0002c0003t0001g0329a0002c0003t0001g0330 | 3 | HG02280.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.906-19707G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628029 | ||||||
| chr11:75628148
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.906-19826G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628148 | ||||||
| chr11:75628210
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906-19888T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628210 | ||||||
| chr11:75628449
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-20127A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628449 | ||||||
| chr11:75628583
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-20261G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628583 | ||||||
| chr11:75628600
|
T | A | 1 | a0002c0003t0001g0302 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.906-20278A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628600 | ||||||
| chr11:75628761
|
A | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG03516.hp1 HG06807.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-20439T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628761 | ||||||
| chr11:75628793
|
T | C | 20 | a0002c0002t0001g0286a0002c0003t0001g0022a0002c0003t0001g0023others(17): Show | 22 | HG00621.hp1 HG01928.hp1 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.906-20471A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75628793 | ||||||
| chr11:75629067
|
C | T | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.906-20745G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629067 | ||||||
| chr11:75629101
|
T | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.906-20779A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629101 | ||||||
| chr11:75629142
|
C | T | 2 | a0002c0003t0001g0290a0002c0003t0001g0299 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.906-20820G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629142 | ||||||
| chr11:75629235
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.906-20913C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629235 | ||||||
| chr11:75629365
|
G | GC | 3 | a0001c0001t0001g0134a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01261.hp2 HG02602.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.906-21044_906-2104 others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629365 | ||||||
| chr11:75629725
|
G | C | 1 | a0001c0004t0001g0119 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.906-21403C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629725 | ||||||
| chr11:75629769
|
G | T | 1 | a0002c0003t0001g0276 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-21447C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629769 | ||||||
| chr11:75629770
|
T | A | 1 | a0002c0003t0001g0276 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-21448A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629770 | ||||||
| chr11:75629771
|
A | T | 1 | a0002c0003t0001g0276 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-21449T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75629771 | ||||||
| chr11:75630017
|
A | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.906-21695T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630017 | ||||||
| chr11:75630141
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.906-21819G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630141 | ||||||
| chr11:75630142
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-21820C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630142 | ||||||
| chr11:75630180
|
G | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-21858C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630180 | ||||||
| chr11:75630272
|
T | C | 1 | a0001c0009t0001g0028 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.906-21950A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630272 | ||||||
| chr11:75630376
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0169a0002c0003t0001g0276others(1): Show | 4 | HG03209.hp1 NA19072.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-22054G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630376 | ||||||
| chr11:75630377
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(261): Show | 305 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.906-22055T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630377 | ||||||
| chr11:75630619
|
C | T | 2 | a0002c0003t0001g0282a0002c0003t0001g0283 | 2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.906-22297G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630619 | ||||||
| chr11:75630716
|
T | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 52 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.906-22394A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630716 | ||||||
| chr11:75630795
|
C | T | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.906-22473G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630795 | ||||||
| chr11:75630808
|
T | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-22486A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630808 | ||||||
| chr11:75630901
|
C | T | 9 | a0002c0003t0001g0310a0002c0003t0001g0311a0002c0003t0001g0313others(6): Show | 9 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-22579G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75630901 | ||||||
| chr11:75631069
|
G | A | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.906-22747C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631069 | ||||||
| chr11:75631283
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.906-22961A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631283 | ||||||
| chr11:75631482
|
T | C | 1 | a0002c0003t0001g0298 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.906-23160A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631482 | ||||||
| chr11:75631807
|
C | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(134): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.906-23485G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631807 | ||||||
| chr11:75631820
|
CACTGGGT others(8): Show |
C | 1 | a0002c0003t0001g0319 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.906-23513_906-2349 others(19): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75631820 | ||||||
| chr11:75632106
|
A | G | 1 | a0002c0002t0001g0322 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.906-23784T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632106 | ||||||
| chr11:75632126
|
C | T | 1 | a0002c0003t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.906-23804G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632126 | ||||||
| chr11:75632413
|
C | G | 8 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0192others(5): Show | 9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.906-24091G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632413 | ||||||
| chr11:75632484
|
G | A | 73 | a0002c0002t0001g0286a0002c0002t0001g0303a0002c0002t0001g0306others(70): Show | 82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.906-24162C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632484 | ||||||
| chr11:75632492
|
A | T | 1 | a0002c0003t0001g0276 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-24170T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632492 | ||||||
| chr11:75632737
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.906-24415C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75632737 | ||||||
| chr11:75633010
|
CT | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 62 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.906-24689delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633010 | ||||||
| chr11:75633031
|
GAAGAGAC others(5): Show |
G | 1 | a0002c0003t0001g0276 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.906-24721_906-2471 others(16): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633031 | ||||||
| chr11:75633117
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.906-24795T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633117 | ||||||
| chr11:75633409
|
T | C | 4 | a0001c0004t0001g0045a0001c0004t0001g0046a0001c0004t0001g0047others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-25087A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633409 | ||||||
| chr11:75633596
|
A | T | 1 | a0002c0002t0001g0303 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.906-25274T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633596 | ||||||
| chr11:75633819
|
G | A | 9 | a0002c0003t0001g0310a0002c0003t0001g0311a0002c0003t0001g0313others(6): Show | 9 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-25497C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633819 | ||||||
| chr11:75633861
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(125): Show | 150 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.906-25539T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633861 | ||||||
| chr11:75633903
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.906-25581G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75633903 | ||||||
| chr11:75634363
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.906-26041C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75634363 | ||||||
| chr11:75634395
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.906-26073C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75634395 | ||||||
| chr11:75634750
|
C | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.906-26428G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75634750 | ||||||
| chr11:75635027
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.906-26705A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635027 | ||||||
| chr11:75635061
|
C | T | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.906-26739G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635061 | ||||||
| chr11:75635062
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.906-26740C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635062 | ||||||
| chr11:75635270
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(52): Show | 68 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.906-26948A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635270 | ||||||
| chr11:75635303
|
T | C | 3 | a0002c0003t0001g0023a0002c0003t0001g0287a0002c0003t0001g0288 | 4 | HG00621.hp1 HG02015.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-26981A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635303 | ||||||
| chr11:75635304
|
TA | T | 3 | a0002c0003t0001g0023a0002c0003t0001g0287a0002c0003t0001g0288 | 4 | HG00621.hp1 HG02015.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-26983delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635304 | ||||||
| chr11:75635335
|
A | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.906-27013T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635335 | ||||||
| chr11:75635477
|
CA | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-27156delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635477 | ||||||
| chr11:75635515
|
T | C | 1 | a0002c0002t0001g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.906-27193A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635515 | ||||||
| chr11:75635652
|
C | T | 7 | a0002c0002t0001g0020a0002c0002t0001g0221a0002c0002t0001g0228others(4): Show | 8 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.906-27330G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635652 | ||||||
| chr11:75635722
|
T | C | 2 | a0001c0001t0001g0137a0001c0004t0001g0138 | 2 | HG02523.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.906-27400A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75635722 | ||||||
| chr11:75636065
|
C | A | 1 | a0002c0003t0001g0278 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.906-27743G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636065 | ||||||
| chr11:75636210
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-27888T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636210 | ||||||
| chr11:75636357
|
CT | C | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-28036delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636357 | ||||||
| chr11:75636386
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.906-28064A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636386 | ||||||
| chr11:75636408
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.906-28086T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636408 | ||||||
| chr11:75636797
|
A | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.906-28475T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636797 | ||||||
| chr11:75636909
|
T | C | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-28587A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75636909 | ||||||
| chr11:75637118
|
T | G | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.906-28796A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637118 | ||||||
| chr11:75637165
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.906-28843A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637165 | ||||||
| chr11:75637293
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.906-28971G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637293 | ||||||
| chr11:75637405
|
T | G | 3 | a0002c0003t0001g0025a0002c0003t0001g0304a0006c0017t0001g0309 | 4 | HG01243.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-29083A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637405 | ||||||
| chr11:75637504
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.906-29182A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637504 | ||||||
| chr11:75637580
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.906-29258T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637580 | ||||||
| chr11:75637866
|
GGGAAGGA others(1): Show |
G | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.906-29552_906-2954 others(12): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75637866 | ||||||
| chr11:75638011
|
T | C | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+29454A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638011 | ||||||
| chr11:75638157
|
T | TGCTCTGC others(3): Show |
8 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0192others(5): Show | 9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+29307_905+2930 others(14): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638157 | ||||||
| chr11:75638205
|
C | G | 23 | a0002c0002t0001g0286a0002c0003t0001g0022a0002c0003t0001g0023others(20): Show | 26 | HG00621.hp1 HG01243.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.905+29260G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638205 | ||||||
| chr11:75638243
|
A | G | 1 | a0002c0003t0001g0025 | 2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.905+29222T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638243 | ||||||
| chr11:75638438
|
C | T | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+29027G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638438 | ||||||
| chr11:75638458
|
A | C | 1 | a0002c0002t0001g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.905+29007T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638458 | ||||||
| chr11:75638781
|
C | A | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+28684G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638781 | ||||||
| chr11:75638968
|
C | T | 266 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(263): Show | 307 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.905+28497G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638968 | ||||||
| chr11:75638984
|
C | A | 40 | a0001c0001t0001g0117a0001c0001t0001g0129a0001c0001t0001g0154others(37): Show | 52 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.905+28481G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638984 | ||||||
| chr11:75638986
|
T | C | 2 | a0002c0003t0001g0276a0002c0003t0001g0277 | 2 | NA19072.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.905+28479A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75638986 | ||||||
| chr11:75639094
|
A | G | 3 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0004t0001g0138 | 3 | HG02523.hp2 NA18952.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.905+28371T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639094 | ||||||
| chr11:75639122
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+28343T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639122 | ||||||
| chr11:75639358
|
G | A | 1 | a0002c0002t0001g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28107C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639358 | ||||||
| chr11:75639359
|
G | A | 1 | a0002c0002t0001g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28106C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639359 | ||||||
| chr11:75639360
|
A | C | 1 | a0002c0002t0001g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28105T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639360 | ||||||
| chr11:75639361
|
A | T | 1 | a0002c0002t0001g0226 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.905+28104T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639361 | ||||||
| chr11:75639805
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.905+27660C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639805 | ||||||
| chr11:75639826
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 62 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.905+27639A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75639826 | ||||||
| chr11:75640018
|
C | T | 1 | a0001c0004t0001g0110 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.905+27447G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640018 | ||||||
| chr11:75640189
|
A | AC | 43 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(40): Show | 55 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.905+27275dupG | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640189 | ||||||
| chr11:75640195
|
C | A | 1 | a0001c0001t0001g0070 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.905+27270G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640195 | ||||||
| chr11:75640195
|
C | CA | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+27269_905+2727 others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640195 | ||||||
| chr11:75640197
|
A | C | 1 | a0001c0004t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.905+27268T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640197 | ||||||
| chr11:75640213
|
AC | A | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+27251delG | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640213 | ||||||
| chr11:75640469
|
T | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+26996A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640469 | ||||||
| chr11:75640611
|
T | C | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+26854A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640611 | ||||||
| chr11:75640654
|
A | C | 1 | a0002c0002t0001g0321 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.905+26811T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640654 | ||||||
| chr11:75640687
|
G | A | 1 | a0001c0004t0001g0132 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.905+26778C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640687 | ||||||
| chr11:75640744
|
C | T | 1 | a0001c0004t0001g0059 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.905+26721G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640744 | ||||||
| chr11:75640851
|
T | G | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+26614A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640851 | ||||||
| chr11:75640867
|
C | T | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+26598G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640867 | ||||||
| chr11:75640868
|
A | G | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+26597T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75640868 | ||||||
| chr11:75641035
|
G | A | 1 | a0002c0002t0001g0257 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.905+26430C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641035 | ||||||
| chr11:75641147
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.905+26318A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641147 | ||||||
| chr11:75641339
|
T | TG | 13 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0106others(10): Show | 13 | HG00609.hp1 HG01169.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+26125dupC | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641339 | ||||||
| chr11:75641376
|
T | C | 1 | a0001c0004t0001g0157 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.905+26089A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641376 | ||||||
| chr11:75641433
|
T | C | 2 | a0002c0003t0001g0198a0002c0003t0001g0199 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.905+26032A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641433 | ||||||
| chr11:75641483
|
T | TA | 69 | a0001c0001t0001g0011a0001c0001t0001g0038a0001c0001t0001g0039others(66): Show | 82 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+25981dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641483 | ||||||
| chr11:75641484
|
A | T | 1 | a0002c0002t0001g0225 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.905+25981T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641484 | ||||||
| chr11:75641540
|
T | G | 2 | a0002c0003t0001g0280a0002c0003t0001g0281 | 2 | NA18959.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.905+25925A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641540 | ||||||
| chr11:75641588
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+25877C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75641588 | ||||||
| chr11:75642069
|
C | G | 8 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0192others(5): Show | 9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+25396G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642069 | ||||||
| chr11:75642095
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+25370G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642095 | ||||||
| chr11:75642245
|
T | C | 1 | a0001c0004t0001g0124 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.905+25220A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642245 | ||||||
| chr11:75642424
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.905+25041G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642424 | ||||||
| chr11:75642623
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+24842T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642623 | ||||||
| chr11:75642644
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+24821T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642644 | ||||||
| chr11:75642721
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+24744G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642721 | ||||||
| chr11:75642817
|
C | T | 1 | a0002c0019t0001g0336 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.905+24648G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642817 | ||||||
| chr11:75642846
|
C | A | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+24619G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642846 | ||||||
| chr11:75642899
|
C | T | 1 | a0001c0007t0001g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.905+24566G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75642899 | ||||||
| chr11:75643068
|
C | A | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+24397G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643068 | ||||||
| chr11:75643213
|
G | C | 1 | a0002c0003t0001g0271 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.905+24252C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643213 | ||||||
| chr11:75643218
|
T | TTA | 4 | a0002c0002t0001g0255a0002c0003t0001g0275a0002c0003t0001g0279others(1): Show | 4 | HG02132.hp1 HG03491.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+24245_905+2424 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643218 | ||||||
| chr11:75643220
|
A | T | 6 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035others(3): Show | 7 | HG02559.hp1 HG02647.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.905+24245T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643220 | ||||||
| chr11:75643241
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.905+24224A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643241 | ||||||
| chr11:75643410
|
C | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+24055G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643410 | ||||||
| chr11:75643531
|
T | C | 3 | a0002c0003t0001g0023a0002c0003t0001g0287a0002c0003t0001g0288 | 4 | HG00621.hp1 HG02015.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+23934A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643531 | ||||||
| chr11:75643638
|
G | C | 1 | a0001c0001t0001g0151 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.905+23827C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643638 | ||||||
| chr11:75643773
|
C | T | 1 | a0002c0002t0001g0216 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.905+23692G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75643773 | ||||||
| chr11:75644045
|
T | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0192others(5): Show | 9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+23420A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644045 | ||||||
| chr11:75644168
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+23297G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644168 | ||||||
| chr11:75644307
|
A | T | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+23158T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644307 | ||||||
| chr11:75644491
|
A | C | 3 | a0002c0002t0001g0247a0002c0002t0001g0248a0002c0014t0001g0224 | 3 | HG03831.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.905+22974T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644491 | ||||||
| chr11:75644590
|
T | C | 1 | a0002c0003t0001g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.905+22875A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644590 | ||||||
| chr11:75644750
|
T | G | 1 | a0002c0003t0001g0302 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.905+22715A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644750 | ||||||
| chr11:75644769
|
T | C | 1 | a0002c0003t0001g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.905+22696A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644769 | ||||||
| chr11:75644829
|
C | A | 2 | a0001c0004t0001g0131a0001c0004t0001g0132 | 2 | HG00140.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.905+22636G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644829 | ||||||
| chr11:75644835
|
G | A | 1 | a0002c0003t0001g0304 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.905+22630C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644835 | ||||||
| chr11:75644934
|
T | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 58 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.905+22531A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644934 | ||||||
| chr11:75644962
|
G | A | 3 | a0002c0003t0001g0275a0002c0003t0001g0279a0002c0003t0001g0296 | 3 | HG02132.hp1 NA18954.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.905+22503C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75644962 | ||||||
| chr11:75645061
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+22404C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645061 | ||||||
| chr11:75645107
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.905+22358C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645107 | ||||||
| chr11:75645132
|
G | C | 3 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA19072.hp1 NA19081.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.905+22333C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645132 | ||||||
| chr11:75645283
|
G | A | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+22182C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645283 | ||||||
| chr11:75645290
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+22175A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645290 | ||||||
| chr11:75645669
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+21796G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645669 | ||||||
| chr11:75645875
|
G | C | 7 | a0002c0002t0001g0303a0002c0003t0001g0298a0002c0003t0001g0317others(4): Show | 7 | HG02280.hp1 HG02970.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+21590C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75645875 | ||||||
| chr11:75646214
|
C | T | 4 | a0001c0004t0001g0108a0001c0004t0001g0109a0001c0004t0001g0121others(1): Show | 4 | HG02015.hp2 HG03704.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+21251G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646214 | ||||||
| chr11:75646239
|
A | C | 1 | a0002c0002t0001g0320 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.905+21226T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646239 | ||||||
| chr11:75646305
|
G | C | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+21160C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646305 | ||||||
| chr11:75646412
|
AGCACTTT others(2): Show |
A | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+21044_905+2105 others(13): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646412 | ||||||
| chr11:75646460
|
A | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+21005T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646460 | ||||||
| chr11:75646486
|
A | C | 73 | a0002c0002t0001g0286a0002c0002t0001g0303a0002c0002t0001g0306others(70): Show | 82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+20979T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646486 | ||||||
| chr11:75646499
|
T | TA | 27 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0001g0070others(24): Show | 28 | HG00140.hp1 HG00423.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.905+20965dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | ||||||
| chr11:75646499
|
T | TAA | 35 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0017others(32): Show | 46 | HG00558.hp2 HG02056.hp1 HG02145.hp1 others(43): Show |
intron_variant | MODIFIER | c.905+20964_905+2096 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | ||||||
| chr11:75646499
|
T | TAAA | 6 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(3): Show | 7 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+20963_905+2096 others(7): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | ||||||
| chr11:75646499
|
TA | T | 18 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0068others(15): Show | 19 | HG01168.hp1 HG02895.hp2 HG02965.hp2 others(16): Show |
intron_variant | MODIFIER | c.905+20965delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646499 | ||||||
| chr11:75646525
|
G | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(52): Show | 68 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.905+20940C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646525 | ||||||
| chr11:75646559
|
C | T | 73 | a0002c0002t0001g0286a0002c0002t0001g0303a0002c0002t0001g0306others(70): Show | 82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+20906G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646559 | ||||||
| chr11:75646603
|
G | A | 3 | a0002c0003t0001g0298a0002c0003t0001g0317a0002c0003t0001g0318 | 3 | HG06807.hp2 NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.905+20862C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646603 | ||||||
| chr11:75646708
|
G | C | 3 | a0002c0003t0001g0282a0002c0003t0001g0283a0002c0003t0001g0305 | 3 | HG02257.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.905+20757C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646708 | ||||||
| chr11:75646776
|
C | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 61 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.905+20689G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646776 | ||||||
| chr11:75646840
|
T | G | 1 | a0002c0002t0001g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.905+20625A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646840 | ||||||
| chr11:75646948
|
T | G | 2 | a0002c0002t0001g0247a0002c0002t0001g0248 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.905+20517A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646948 | ||||||
| chr11:75646955
|
T | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.905+20510A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646955 | ||||||
| chr11:75646985
|
C | CT | 237 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(234): Show | 273 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.905+20479dupA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646985 | ||||||
| chr11:75646985
|
C | CTT | 26 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028others(23): Show | 31 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.905+20478_905+2047 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75646985 | ||||||
| chr11:75647083
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+20382A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647083 | ||||||
| chr11:75647171
|
A | AT | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+20293dupA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647171 | ||||||
| chr11:75647272
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+20193A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647272 | ||||||
| chr11:75647298
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18946.hp2 NA18964.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.905+20167T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647298 | ||||||
| chr11:75647326
|
T | TA | 7 | a0001c0001t0001g0147a0002c0002t0001g0303a0002c0003t0001g0288others(4): Show | 7 | HG01496.hp2 HG02970.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+20138dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647326 | ||||||
| chr11:75647347
|
C | CA | 80 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(77): Show | 86 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.905+20117dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | ||||||
| chr11:75647347
|
C | CAA | 12 | a0001c0001t0001g0033a0001c0001t0001g0043a0001c0001t0001g0068others(9): Show | 12 | HG02055.hp1 HG02257.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.905+20116_905+2011 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | ||||||
| chr11:75647347
|
CA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(74): Show | 95 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.905+20117delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | ||||||
| chr11:75647347
|
CAA | C | 24 | a0001c0001t0001g0037a0002c0002t0001g0286a0002c0003t0001g0022others(21): Show | 27 | HG00621.hp1 HG01243.hp1 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.905+20116_905+2011 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | ||||||
| chr11:75647347
|
CAAA | C | 9 | a0001c0001t0001g0197a0002c0002t0001g0200a0002c0002t0001g0201others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+20115_905+2011 others(7): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647347 | ||||||
| chr11:75647402
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+20063C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647402 | ||||||
| chr11:75647529
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+19936G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647529 | ||||||
| chr11:75647561
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG03516.hp1 HG06807.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+19904T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647561 | ||||||
| chr11:75647574
|
A | C | 1 | a0009c0010t0001g0030 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.905+19891T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647574 | ||||||
| chr11:75647612
|
G | A | 1 | a0001c0004t0001g0126 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.905+19853C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647612 | ||||||
| chr11:75647975
|
A | T | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+19490T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75647975 | ||||||
| chr11:75648006
|
G | A | 1 | a0002c0002t0001g0308 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.905+19459C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648006 | ||||||
| chr11:75648074
|
T | C | 2 | a0002c0002t0001g0254a0002c0002t0001g0255 | 2 | HG02602.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.905+19391A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648074 | ||||||
| chr11:75648130
|
T | C | 44 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0013others(41): Show | 49 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.905+19335A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648130 | ||||||
| chr11:75648137
|
C | T | 2 | a0002c0002t0001g0021a0002c0002t0001g0264 | 3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.905+19328G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648137 | ||||||
| chr11:75648282
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+19183G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648282 | ||||||
| chr11:75648411
|
T | C | 3 | a0002c0003t0001g0026a0002c0003t0001g0315a0002c0003t0001g0316 | 4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+19054A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648411 | ||||||
| chr11:75648454
|
A | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+19011T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648454 | ||||||
| chr11:75648484
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+18981A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648484 | ||||||
| chr11:75648486
|
A | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+18979T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648486 | ||||||
| chr11:75648489
|
C | A | 73 | a0002c0002t0001g0286a0002c0002t0001g0303a0002c0002t0001g0306others(70): Show | 82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+18976G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648489 | ||||||
| chr11:75648498
|
A | AAAAC | 14 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(11): Show | 15 | HG01928.hp1 HG02273.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+18963_905+1896 others(8): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648498 | ||||||
| chr11:75648498
|
AAAAC | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(42): Show | 57 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.905+18963_905+1896 others(8): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648498 | ||||||
| chr11:75648564
|
T | A | 3 | a0002c0003t0001g0025a0002c0003t0001g0304a0006c0017t0001g0309 | 4 | HG01243.hp1 HG02896.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+18901A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648564 | ||||||
| chr11:75648575
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+18890T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75648575 | ||||||
| chr11:75649190
|
AT | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+18274delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649190 | ||||||
| chr11:75649461
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+18004C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649461 | ||||||
| chr11:75649464
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+18001C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649464 | ||||||
| chr11:75649473
|
T | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+17992A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649473 | ||||||
| chr11:75649502
|
A | G | 3 | a0002c0003t0001g0282a0002c0003t0001g0283a0002c0003t0001g0305 | 3 | HG02257.hp1 HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.905+17963T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649502 | ||||||
| chr11:75649505
|
A | G | 1 | a0002c0003t0001g0315 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.905+17960T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649505 | ||||||
| chr11:75649687
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905+17778G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649687 | ||||||
| chr11:75649827
|
C | T | 2 | a0001c0001t0001g0058a0001c0004t0001g0057 | 2 | HG01255.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.905+17638G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649827 | ||||||
| chr11:75649855
|
G | A | 1 | a0001c0004t0001g0181 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.905+17610C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649855 | ||||||
| chr11:75649966
|
G | C | 2 | a0002c0002t0001g0021a0002c0002t0001g0264 | 3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.905+17499C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649966 | ||||||
| chr11:75649983
|
C | T | 3 | a0002c0003t0001g0026a0002c0003t0001g0315a0002c0003t0001g0316 | 4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+17482G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75649983 | ||||||
| chr11:75650080
|
C | T | 15 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0037others(12): Show | 16 | HG02109.hp1 HG02486.hp2 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.905+17385G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650080 | ||||||
| chr11:75650108
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.905+17357T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650108 | ||||||
| chr11:75650525
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905+16940A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650525 | ||||||
| chr11:75650563
|
G | C | 1 | a0002c0003t0001g0305 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.905+16902C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650563 | ||||||
| chr11:75650996
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(264): Show | 308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.905+16469A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75650996 | ||||||
| chr11:75651060
|
A | G | 1 | a0002c0003t0001g0311 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.905+16405T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651060 | ||||||
| chr11:75651244
|
G | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0192a0001c0004t0001g0034others(1): Show | 4 | HG02886.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+16221C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651244 | ||||||
| chr11:75651483
|
G | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(52): Show | 68 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.905+15982C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651483 | ||||||
| chr11:75651530
|
T | TA | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+15934dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651530 | ||||||
| chr11:75651759
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.905+15706C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651759 | ||||||
| chr11:75651788
|
C | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0192others(5): Show | 9 | HG02630.hp2 HG02886.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.905+15677G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651788 | ||||||
| chr11:75651938
|
G | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+15527C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75651938 | ||||||
| chr11:75652024
|
C | T | 1 | a0001c0012t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+15441G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652024 | ||||||
| chr11:75652056
|
T | A | 6 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(3): Show | 6 | HG02056.hp1 NA18946.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.905+15409A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652056 | ||||||
| chr11:75652074
|
C | T | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0152 | 3 | HG03516.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.905+15391G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652074 | ||||||
| chr11:75652167
|
T | G | 1 | a0002c0003t0001g0278 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.905+15298A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652167 | ||||||
| chr11:75652273
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+15192C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652273 | ||||||
| chr11:75652365
|
T | C | 1 | a0001c0004t0001g0127 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.905+15100A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652365 | ||||||
| chr11:75652408
|
C | A | 1 | a0002c0002t0001g0215 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.905+15057G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652408 | ||||||
| chr11:75652580
|
G | A | 7 | a0001c0001t0001g0037a0002c0002t0001g0200a0002c0002t0001g0201others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+14885C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652580 | ||||||
| chr11:75652632
|
T | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+14833A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652632 | ||||||
| chr11:75652836
|
G | GA | 40 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(37): Show | 52 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.905+14628dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652836 | ||||||
| chr11:75652849
|
A | G | 2 | a0002c0003t0001g0280a0002c0003t0001g0281 | 2 | NA18959.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.905+14616T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652849 | ||||||
| chr11:75652973
|
A | G | 2 | a0002c0002t0001g0214a0002c0002t0001g0215 | 2 | NA19054.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.905+14492T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75652973 | ||||||
| chr11:75653026
|
C | A | 2 | a0001c0001t0001g0042a0001c0004t0001g0041 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.905+14439G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653026 | ||||||
| chr11:75653168
|
C | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+14297G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653168 | ||||||
| chr11:75653264
|
C | A | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+14201G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653264 | ||||||
| chr11:75653269
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+14196A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653269 | ||||||
| chr11:75653290
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.905+14175G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653290 | ||||||
| chr11:75653312
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0104 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.905+14153A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653312 | ||||||
| chr11:75653567
|
T | C | 2 | a0001c0001t0001g0159a0001c0004t0001g0160 | 2 | HG01255.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.905+13898A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653567 | ||||||
| chr11:75653729
|
T | C | 1 | a0002c0002t0001g0257 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.905+13736A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653729 | ||||||
| chr11:75653962
|
C | T | 2 | a0002c0002t0001g0212a0002c0002t0001g0213 | 2 | HG03927.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.905+13503G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653962 | ||||||
| chr11:75653994
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.905+13471A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75653994 | ||||||
| chr11:75654377
|
T | A | 1 | a0001c0001t0001g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.905+13088A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654377 | ||||||
| chr11:75654489
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+12976A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654489 | ||||||
| chr11:75654728
|
G | A | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+12737C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654728 | ||||||
| chr11:75654755
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.905+12710G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654755 | ||||||
| chr11:75654864
|
G | A | 1 | a0001c0004t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.905+12601C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75654864 | ||||||
| chr11:75655165
|
T | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+12300A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655165 | ||||||
| chr11:75655240
|
C | T | 1 | a0002c0003t0001g0279 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.905+12225G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655240 | ||||||
| chr11:75655344
|
A | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 5 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.905+12121T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655344 | ||||||
| chr11:75655517
|
C | T | 35 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 47 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.905+11948G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655517 | ||||||
| chr11:75655556
|
C | A | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+11909G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655556 | ||||||
| chr11:75655606
|
G | C | 2 | a0002c0002t0001g0306a0002c0002t0001g0307 | 2 | NA18941.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.905+11859C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655606 | ||||||
| chr11:75655621
|
G | T | 1 | a0002c0003t0001g0310 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.905+11844C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655621 | ||||||
| chr11:75655653
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.905+11812C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655653 | ||||||
| chr11:75655976
|
T | C | 1 | a0001c0012t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+11489A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75655976 | ||||||
| chr11:75656184
|
G | T | 7 | a0001c0001t0001g0037a0002c0002t0001g0200a0002c0002t0001g0201others(4): Show | 7 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+11281C>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75656184 | ||||||
| chr11:75656244
|
C | G | 9 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0192others(6): Show | 10 | HG00639.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.905+11221G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75656244 | ||||||
| chr11:75656694
|
T | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+10771A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75656694 | ||||||
| chr11:75657108
|
CTAT | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(31): Show | 45 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.905+10354_905+1035 others(7): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657108 | ||||||
| chr11:75657110
|
AT | A | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0197others(6): Show | 10 | HG02055.hp2 HG02630.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.905+10354delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657110 | ||||||
| chr11:75657110
|
ATT | A | 9 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035others(6): Show | 9 | HG02109.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.905+10353_905+1035 others(6): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657110 | ||||||
| chr11:75657110
|
ATTTT | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+10351_905+1035 others(8): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657110 | ||||||
| chr11:75657300
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+10165G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657300 | ||||||
| chr11:75657311
|
C | T | 4 | a0002c0002t0001g0204a0002c0002t0001g0209a0002c0002t0001g0211others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+10154G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657311 | ||||||
| chr11:75657366
|
G | A | 1 | a0002c0002t0001g0258 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.905+10099C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657366 | ||||||
| chr11:75657959
|
A | G | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+9506T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75657959 | ||||||
| chr11:75658308
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(33): Show | 48 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.905+9157G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658308 | ||||||
| chr11:75658397
|
C | CA | 73 | a0002c0002t0001g0286a0002c0002t0001g0303a0002c0002t0001g0306others(70): Show | 82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+9067_905+9068i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658397 | ||||||
| chr11:75658399
|
C | CA | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0153 | 3 | HG00423.hp1 HG00609.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.905+9065_905+9066i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658399 | ||||||
| chr11:75658399
|
C | CT | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+9065_905+9066i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658399 | ||||||
| chr11:75658399
|
C | T | 2 | a0002c0003t0001g0276a0002c0003t0001g0277 | 2 | NA19072.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.905+9066G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658399 | ||||||
| chr11:75658400
|
C | CG | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+9064_905+9065i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658400 | ||||||
| chr11:75658404
|
C | CT | 175 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(172): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.905+9060_905+9061i others(3): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658404 | ||||||
| chr11:75658404
|
C | G | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+9061G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658404 | ||||||
| chr11:75658404
|
C | T | 89 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(86): Show | 99 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.905+9061G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658404 | ||||||
| chr11:75658405
|
G | A | 1 | a0006c0017t0001g0309 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.905+9060C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658405 | ||||||
| chr11:75658406
|
C | T | 1 | a0002c0003t0001g0275 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.905+9059G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658406 | ||||||
| chr11:75658411
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.905+9054C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658411 | ||||||
| chr11:75658830
|
C | A | 3 | a0002c0003t0001g0026a0002c0003t0001g0315a0002c0003t0001g0316 | 4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+8635G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658830 | ||||||
| chr11:75658900
|
A | C | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+8565T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658900 | ||||||
| chr11:75658938
|
T | C | 1 | a0001c0004t0001g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.905+8527A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75658938 | ||||||
| chr11:75659003
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.905+8462T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659003 | ||||||
| chr11:75659264
|
C | A | 1 | a0002c0002t0001g0259 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.905+8201G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659264 | ||||||
| chr11:75659274
|
G | A | 4 | a0001c0001t0001g0129a0001c0004t0001g0130a0001c0004t0001g0131others(1): Show | 4 | HG00140.hp2 HG00738.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+8191C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659274 | ||||||
| chr11:75659352
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.905+8113G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659352 | ||||||
| chr11:75659475
|
A | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(51): Show | 67 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.905+7990T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659475 | ||||||
| chr11:75659883
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.905+7582A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659883 | ||||||
| chr11:75659943
|
C | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(264): Show | 308 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.905+7522G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659943 | ||||||
| chr11:75659991
|
T | C | 4 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(1): Show | 4 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+7474A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659991 | ||||||
| chr11:75659996
|
C | T | 3 | a0001c0001t0001g0036a0001c0004t0001g0034a0001c0004t0001g0035 | 3 | HG02886.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.905+7469G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75659996 | ||||||
| chr11:75660137
|
T | C | 40 | a0001c0001t0001g0117a0001c0001t0001g0129a0001c0001t0001g0154others(37): Show | 52 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.905+7328A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660137 | ||||||
| chr11:75660142
|
T | C | 1 | a0002c0002t0001g0260 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.905+7323A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660142 | ||||||
| chr11:75660309
|
C | G | 18 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(15): Show | 29 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.905+7156G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660309 | ||||||
| chr11:75660312
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+7153G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660312 | ||||||
| chr11:75660412
|
A | G | 1 | a0001c0012t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+7053T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660412 | ||||||
| chr11:75660534
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+6931A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660534 | ||||||
| chr11:75660659
|
C | T | 4 | a0001c0004t0001g0045a0001c0004t0001g0046a0001c0004t0001g0047others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+6806G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660659 | ||||||
| chr11:75660809
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+6656G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660809 | ||||||
| chr11:75660882
|
T | G | 3 | a0002c0003t0001g0026a0002c0003t0001g0315a0002c0003t0001g0316 | 4 | HG02559.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+6583A>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660882 | ||||||
| chr11:75660966
|
T | C | 18 | a0002c0002t0001g0312a0002c0002t0001g0320a0002c0002t0001g0321others(15): Show | 19 | HG00323.hp1 HG02074.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.905+6499A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75660966 | ||||||
| chr11:75661009
|
T | C | 15 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01099.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+6456A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661009 | ||||||
| chr11:75661019
|
GA | G | 5 | a0002c0003t0001g0265a0002c0003t0001g0266a0002c0003t0001g0267others(2): Show | 5 | NA18942.hp1 NA18975.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.905+6445delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661019 | ||||||
| chr11:75661178
|
G | C | 2 | a0002c0003t0001g0317a0002c0003t0001g0318 | 2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.905+6287C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661178 | ||||||
| chr11:75661212
|
T | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 62 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.905+6253A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661212 | ||||||
| chr11:75661421
|
A | G | 73 | a0002c0002t0001g0286a0002c0002t0001g0303a0002c0002t0001g0306others(70): Show | 82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.905+6044T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661421 | ||||||
| chr11:75661512
|
A | C | 4 | a0002c0002t0001g0204a0002c0002t0001g0209a0002c0002t0001g0211others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+5953T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661512 | ||||||
| chr11:75661669
|
A | G | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 42 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.905+5796T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661669 | ||||||
| chr11:75661730
|
T | A | 1 | a0001c0004t0001g0148 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.905+5735A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661730 | ||||||
| chr11:75661779
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.905+5686T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661779 | ||||||
| chr11:75661833
|
CA | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+5631delT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661833 | ||||||
| chr11:75661835
|
A | C | 1 | a0001c0001t0001g0043 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.905+5630T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75661835 | ||||||
| chr11:75662071
|
A | C | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+5394T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662071 | ||||||
| chr11:75662174
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+5291A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662174 | ||||||
| chr11:75662391
|
C | T | 1 | a0002c0002t0001g0325 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905+5074G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662391 | ||||||
| chr11:75662571
|
G | C | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.905+4894C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662571 | ||||||
| chr11:75662646
|
G | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG03516.hp1 HG06807.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.905+4819C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662646 | ||||||
| chr11:75662962
|
CT | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(119): Show | 144 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.905+4502delA | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75662962 | ||||||
| chr11:75663001
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 62 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.905+4464T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663001 | ||||||
| chr11:75663120
|
C | T | 4 | a0002c0002t0001g0205a0002c0002t0001g0206a0002c0002t0001g0207others(1): Show | 4 | NA18955.hp2 NA18962.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+4345G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663120 | ||||||
| chr11:75663394
|
A | ATTTTCTG others(39): Show |
1 | a0001c0001t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.905+4025_905+4070d others(48): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663394 | ||||||
| chr11:75663531
|
C | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(44): Show | 60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.905+3934G>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663531 | ||||||
| chr11:75663688
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 51 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.905+3777C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75663688 | ||||||
| chr11:75664081
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(44): Show | 60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.905+3384T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664081 | ||||||
| chr11:75664097
|
C | T | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+3368G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664097 | ||||||
| chr11:75664134
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(120): Show | 145 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.905+3331G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664134 | ||||||
| chr11:75664185
|
A | G | 4 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0196others(1): Show | 4 | HG02717.hp2 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.905+3280T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664185 | ||||||
| chr11:75664256
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 62 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.905+3209G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664256 | ||||||
| chr11:75664261
|
T | C | 2 | a0002c0002t0001g0262a0002c0002t0001g0263 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.905+3204A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664261 | ||||||
| chr11:75664711
|
A | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(44): Show | 60 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.905+2754T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664711 | ||||||
| chr11:75664865
|
T | A | 1 | a0001c0001t0001g0154 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.905+2600A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664865 | ||||||
| chr11:75664889
|
C | CA | 10 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0191others(7): Show | 11 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.905+2575dupT | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664889 | ||||||
| chr11:75664903
|
G | A | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+2562C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75664903 | ||||||
| chr11:75665093
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+2372C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665093 | ||||||
| chr11:75665286
|
G | C | 5 | a0002c0002t0001g0320a0002c0002t0001g0321a0002c0002t0001g0322others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.905+2179C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665286 | ||||||
| chr11:75665288
|
A | C | 1 | a0001c0001t0001g0039 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.905+2177T>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665288 | ||||||
| chr11:75665590
|
G | C | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+1875C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665590 | ||||||
| chr11:75665702
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+1763A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665702 | ||||||
| chr11:75665825
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.905+1640C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75665825 | ||||||
| chr11:75666115
|
G | A | 2 | a0002c0002t0001g0021a0002c0002t0001g0264 | 3 | HG02055.hp2 HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.905+1350C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666115 | ||||||
| chr11:75666181
|
T | A | 74 | a0002c0002t0001g0273a0002c0002t0001g0286a0002c0002t0001g0303others(71): Show | 83 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.905+1284A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666181 | ||||||
| chr11:75666358
|
AGCT | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02630.hp2 HG03130.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+1104_905+1106d others(5): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666358 | ||||||
| chr11:75666388
|
AAG | A | 3 | a0001c0007t0001g0027a0001c0007t0001g0029a0001c0009t0001g0028 | 3 | HG02717.hp1 HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.905+1075_905+1076d others(4): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666388 | ||||||
| chr11:75666396
|
G | A | 1 | a0002c0002t0001g0325 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905+1069C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666396 | ||||||
| chr11:75666472
|
G | A | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+993C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666472 | ||||||
| chr11:75666490
|
GAACATGT others(40): Show |
G | 1 | a0001c0001t0001g0038 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.905+928_905+974del others(47): Show |
MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666490 | ||||||
| chr11:75666495
|
T | A | 7 | a0001c0001t0001g0159a0001c0004t0001g0003a0001c0004t0001g0156others(4): Show | 12 | HG00099.hp2 HG00735.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.905+970A>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666495 | ||||||
| chr11:75666632
|
G | C | 2 | a0002c0002t0001g0326a0002c0002t0001g0327 | 2 | NA18983.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.905+833C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666632 | ||||||
| chr11:75666684
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(46): Show | 62 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.905+781G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666684 | ||||||
| chr11:75666708
|
A | G | 1 | a0002c0003t0001g0328 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905+757T>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666708 | ||||||
| chr11:75666725
|
T | C | 1 | a0002c0002t0001g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.905+740A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666725 | ||||||
| chr11:75666793
|
C | G | 1 | a0002c0002t0001g0204 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.905+672G>C | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666793 | ||||||
| chr11:75666891
|
A | T | 6 | a0002c0002t0001g0200a0002c0002t0001g0201a0002c0002t0001g0202others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.905+574T>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666891 | ||||||
| chr11:75666958
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+507C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75666958 | ||||||
| chr11:75667101
|
T | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(38): Show | 54 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.905+364A>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667101 | ||||||
| chr11:75667134
|
G | A | 3 | a0002c0003t0001g0328a0002c0003t0001g0329a0002c0003t0001g0330 | 3 | HG02280.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.905+331C>T | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667134 | ||||||
| chr11:75667278
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905+187G>A | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667278 | ||||||
| chr11:75667308
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.905+157C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667308 | ||||||
| chr11:75667403
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.905+62C>G | MAP6 | ENSG00000171533.12 | transcript | ENST00000304771.8 | protein_coding | 1/3 | chr11 | 75667403 |