Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 134526 |
|---|---|
| ensemblid | ENSG00000172497.9 |
| hgncid | 24436 |
| symbol | ACOT12 |
| name | acyl-CoA thioesterase 12 |
| refseq_nuc | NM_130767.3 |
| refseq_prot | NP_570123.1 |
| ensembl_nuc | ENST00000307624.8 |
| ensembl_prot | ENSP00000303246.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 81329996 |
| end | 81394134 |
| strand | - |
| ver | v1.2 |
| region | chr5:81329996-81394134 |
| region5000 | chr5:81324996-81399134 |
| regionname0 | ACOT12_chr5_81329996_81394134 |
| regionname5000 | ACOT12_chr5_81324996_81399134 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 555 | 240 | 72 | 51 | 78 | 11 | 26 | 48 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002 | 0/0 | 555 | 30 | 15 | 10 | 0 | 1 | 4 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0003 | 0/0 | 555 | 5 | 2 | 1 | 0 | 0 | 2 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0004 | 0/0 | 555 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0005 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0006 | 0/0 | 555 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1668 | 238 | 70 | 51 | 78 | 11 | 26 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0002 | 0/0 | 1668 | 29 | 15 | 10 | 0 | 0 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0003 | 0/0 | 1668 | 5 | 2 | 1 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0004 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0005 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0006 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0007 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0008 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| c0009 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 419 | 83 | 9 | 13 | 43 | 4 | 13 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| t0002 | 0/1 | 419 | 78 | 16 | 31 | 17 | 4 | 9 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| t0003 | 0/0 | 419 | 61 | 32 | 13 | 7 | 3 | 6 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| t0004 | 0/0 | 419 | 50 | 28 | 6 | 11 | 1 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| t0005 | 0/0 | 419 | 4 | 4 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| t0006 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| t0007 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0007 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1668 | 238 | 70 | 51 | 78 | 11 | 26 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0005 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0007 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0002 | 0/0 | 1668 | 29 | 15 | 10 | 0 | 0 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0009 | 0/0 | 1668 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0003c0003 | 0/0 | 1668 | 5 | 2 | 1 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0004c0004 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0005c0006 | 0/0 | 1668 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0006c0008 | 0/0 | 1668 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2086 | 74 | 5 | 11 | 43 | 3 | 11 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0001t0002 | 0/1 | 2086 | 61 | 9 | 23 | 17 | 4 | 7 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0001t0003 | 0/0 | 2086 | 55 | 29 | 12 | 7 | 3 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0001t0004 | 0/0 | 2086 | 43 | 23 | 4 | 11 | 1 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0001t0005 | 0/0 | 2086 | 4 | 4 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0001t0006 | 0/0 | 2086 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0005t0003 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0001c0007t0004 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0002t0001 | 0/0 | 2086 | 6 | 4 | 2 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0002t0002 | 0/0 | 2086 | 14 | 6 | 6 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0002t0003 | 0/0 | 2086 | 5 | 2 | 1 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0002t0004 | 0/0 | 2086 | 3 | 2 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0002t0007 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0002c0009t0001 | 0/0 | 2086 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0003c0003t0001 | 0/0 | 2086 | 2 | 0 | 0 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0003c0003t0004 | 0/0 | 2086 | 3 | 2 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0004c0004t0002 | 0/0 | 2086 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0005c0006t0002 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| a0006c0008t0002 | 0/0 | 2086 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | copy fasta | chr5 | 81324996 | 81399134 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0005 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0005t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0007t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0007 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0009t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0003c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0003c0003t0004g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0003c0003t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0004c0004t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0005c0006t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0006c0008t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0028 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0227 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0124 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0199 | EUR | FIN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0231 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01106 | hp2 | a0002 | c0002 | t0004 | g0244 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01243 | hp1 | a0003 | c0003 | t0004 | g0011 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01243 | hp2 | a0006 | c0008 | t0002 | g0134 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01361 | hp2 | a0004 | c0004 | t0002 | g0220 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0161 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0232 | EUR | IBS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0236 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0242 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0099 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0243 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02145 | hp1 | a0003 | c0003 | t0004 | g0198 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CDX | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0107 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0026 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0200 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02886 | hp1 | a0005 | c0006 | t0002 | g0155 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0209 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0023 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0151 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03225 | hp2 | a0001 | c0005 | t0003 | g0202 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0141 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0163 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0249 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0201 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0246 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0007 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0009 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0169 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0247 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18522 | hp2 | a0001 | c0007 | t0004 | g0036 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0037 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ASW | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | ASW | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20805 | hp1 | a0002 | c0009 | t0001 | g0262 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0005 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03471 | hp1 | a0003 | c0003 | t0004 | g0011 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20300 | hp2 | a0002 | c0002 | t0007 | g0211 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0078 | REF | REF | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81330515
|
C | G | 1 | a0003 | 5 | HG01243.hp1 HG02145.hp1 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.1547G>C | p.Ser516Thr | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 1567/2086 | 1547/1668 | 516/555 | chr5 | 81330515 | ||
| chr5:81335823
|
C | T | 1 | a0002 | 30 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(27): Show |
missense_variant | MODERATE | c.1207G>A | p.Ala403Thr | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/15 | 1227/2086 | 1207/1668 | 403/555 | chr5 | 81335823 | ||
| chr5:81343841
|
T | C | 1 | a0005 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1021A>G | p.Ile341Val | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/15 | 1041/2086 | 1021/1668 | 341/555 | chr5 | 81343841 | ||
| chr5:81345970
|
C | T | 1 | a0004 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.688G>A | p.Val230Ile | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/15 | 708/2086 | 688/1668 | 230/555 | chr5 | 81345970 | ||
| chr5:81363805
|
G | A | 1 | a0006 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.343C>T | p.Pro115Ser | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/15 | 363/2086 | 343/1668 | 115/555 | chr5 | 81363805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81335845
|
G | A | 1 | a0001c0005 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1185C>T | p.His395His | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/15 | 1205/2086 | 1185/1668 | 395/555 | chr5 | 81335845 | ||
| chr5:81344993
|
G | A | 1 | a0001c0007 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.822C>T | p.Ala274Ala | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/15 | 842/2086 | 822/1668 | 274/555 | chr5 | 81344993 | ||
| chr5:81394034
|
G | A | 1 | a0002c0009 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.81C>T | p.Ser27Ser | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/15 | 101/2086 | 81/1668 | 27/555 | chr5 | 81394034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81330127
|
C | T | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(8): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 267 | chr5 | 81330127 | |||||
| chr5:81330266
|
C | T | 2 | a0001c0001t0005a0002c0002t0007 | 5 | HG02572.hp2 HG03098.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*128G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 128 | chr5 | 81330266 | |||||
| chr5:81330340
|
G | T | 1 | a0001c0001t0006 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 54 | chr5 | 81330340 | |||||
| chr5:81394134
|
C | A | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(5): Show | 115 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/15 | 20 | chr5 | 81394134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81330678
|
G | C | 2 | a0001c0001t0002g0218a0002c0002t0002g0060 | 2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1519-135C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 14/14 | chr5 | 81330678 | ||||||
| chr5:81331169
|
A | G | 6 | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0001t0001g0081others(3): Show | 6 | NA18965.hp2 NA18971.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392-229T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331169 | ||||||
| chr5:81331259
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1392-319G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331259 | ||||||
| chr5:81331266
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1392-326T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331266 | ||||||
| chr5:81331277
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1392-337G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331277 | ||||||
| chr5:81331298
|
G | A | 2 | a0001c0001t0004g0164a0001c0001t0004g0172 | 2 | HG00673.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1392-358C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331298 | ||||||
| chr5:81331335
|
C | G | 2 | a0001c0001t0002g0059a0001c0001t0002g0232 | 2 | HG01516.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1392-395G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331335 | ||||||
| chr5:81331341
|
T | C | 110 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0051others(107): Show | 115 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1392-401A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331341 | ||||||
| chr5:81331354
|
A | G | 94 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0057others(91): Show | 100 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1392-414T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331354 | ||||||
| chr5:81331403
|
G | T | 11 | a0001c0001t0001g0121a0001c0001t0001g0196a0001c0001t0002g0197others(8): Show | 11 | HG02258.hp1 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1392-463C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331403 | ||||||
| chr5:81331406
|
G | A | 1 | a0002c0002t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1392-466C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331406 | ||||||
| chr5:81331632
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1392-692C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331632 | ||||||
| chr5:81331635
|
C | T | 2 | a0001c0001t0003g0184a0001c0001t0003g0188 | 2 | HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1392-695G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331635 | ||||||
| chr5:81331658
|
G | T | 1 | a0002c0002t0001g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1392-718C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331658 | ||||||
| chr5:81331848
|
T | C | 6 | a0001c0001t0002g0210a0001c0001t0003g0159a0001c0001t0003g0194others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391+629A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331848 | ||||||
| chr5:81331919
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1391+558A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331919 | ||||||
| chr5:81332065
|
A | G | 6 | a0001c0001t0002g0210a0001c0001t0003g0159a0001c0001t0003g0194others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391+412T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332065 | ||||||
| chr5:81332113
|
T | C | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+364A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332113 | ||||||
| chr5:81332120
|
T | C | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+357A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332120 | ||||||
| chr5:81332228
|
C | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+249G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332228 | ||||||
| chr5:81332298
|
T | A | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0001c0001t0004g0162 | 3 | HG02486.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+179A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332298 | ||||||
| chr5:81332385
|
A | G | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0001c0001t0004g0162 | 3 | HG02486.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+92T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332385 | ||||||
| chr5:81332836
|
G | A | 32 | a0001c0001t0001g0053a0001c0001t0001g0109a0001c0001t0001g0131others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1263-231C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81332836 | ||||||
| chr5:81332908
|
T | A | 1 | a0001c0001t0001g0229 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1263-303A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81332908 | ||||||
| chr5:81333063
|
TA | T | 55 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0096others(52): Show | 57 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1263-459delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333063 | ||||||
| chr5:81333082
|
ACAAC | A | 32 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0096others(29): Show | 32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-481_1263-478d others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333082 | ||||||
| chr5:81333083
|
C | T | 26 | a0001c0001t0001g0195a0001c0001t0002g0118a0001c0001t0003g0149others(23): Show | 28 | HG00642.hp2 HG01070.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1263-478G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333083 | ||||||
| chr5:81333087
|
A | T | 32 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0096others(29): Show | 32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-482T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333087 | ||||||
| chr5:81333100
|
A | C | 2 | a0001c0001t0002g0137a0001c0001t0003g0203 | 2 | HG00741.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1263-495T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333100 | ||||||
| chr5:81333119
|
A | G | 5 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0003g0150others(2): Show | 5 | HG02055.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263-514T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333119 | ||||||
| chr5:81333128
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1263-523T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333128 | ||||||
| chr5:81333156
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0002g0125a0001c0001t0003g0240others(1): Show | 4 | HG01192.hp2 HG02148.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-551G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333156 | ||||||
| chr5:81333220
|
A | C | 60 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0096others(57): Show | 62 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1263-615T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333220 | ||||||
| chr5:81333447
|
C | T | 32 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0096others(29): Show | 32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-842G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333447 | ||||||
| chr5:81333514
|
G | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0110 | 2 | NA18982.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1263-909C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333514 | ||||||
| chr5:81333553
|
A | C | 60 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0096others(57): Show | 62 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1263-948T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333553 | ||||||
| chr5:81333626
|
A | T | 32 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0096others(29): Show | 32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-1021T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333626 | ||||||
| chr5:81333680
|
C | T | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1263-1075G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333680 | ||||||
| chr5:81333747
|
A | G | 33 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0090others(30): Show | 33 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1263-1142T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333747 | ||||||
| chr5:81334110
|
A | G | 6 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(3): Show | 6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263-1505T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334110 | ||||||
| chr5:81334123
|
C | T | 6 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(3): Show | 6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263-1518G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334123 | ||||||
| chr5:81334163
|
T | TA | 6 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(3): Show | 6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263-1559dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334163 | ||||||
| chr5:81334245
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1262+1523G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334245 | ||||||
| chr5:81334345
|
C | T | 6 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(3): Show | 6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+1423G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334345 | ||||||
| chr5:81334469
|
G | C | 37 | a0001c0001t0001g0053a0001c0001t0001g0109a0001c0001t0001g0131others(34): Show | 38 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.1262+1299C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334469 | ||||||
| chr5:81334734
|
G | A | 96 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0001g0109others(93): Show | 99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1262+1034C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334734 | ||||||
| chr5:81334854
|
G | A | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0001c0007t0004g0036 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1262+914C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334854 | ||||||
| chr5:81334866
|
G | C | 2 | a0001c0001t0004g0148a0001c0001t0005g0252 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1262+902C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334866 | ||||||
| chr5:81335013
|
G | A | 6 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(3): Show | 6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+755C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335013 | ||||||
| chr5:81335128
|
T | C | 7 | a0002c0002t0002g0007a0002c0002t0002g0058a0002c0002t0002g0061others(4): Show | 8 | HG01099.hp2 HG01109.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1262+640A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335128 | ||||||
| chr5:81335160
|
G | A | 1 | a0001c0001t0004g0025 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1262+608C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335160 | ||||||
| chr5:81335325
|
T | A | 1 | a0002c0002t0003g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1262+443A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335325 | ||||||
| chr5:81335333
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1262+435A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335333 | ||||||
| chr5:81335440
|
C | T | 6 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(3): Show | 6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+328G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335440 | ||||||
| chr5:81335445
|
G | A | 9 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(6): Show | 9 | HG00741.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1262+323C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335445 | ||||||
| chr5:81335502
|
T | C | 99 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(96): Show | 102 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1262+266A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335502 | ||||||
| chr5:81335656
|
A | G | 1 | a0001c0001t0004g0025 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1262+112T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335656 | ||||||
| chr5:81335692
|
G | A | 86 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(83): Show | 89 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1262+76C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335692 | ||||||
| chr5:81335700
|
T | G | 6 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(3): Show | 6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+68A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335700 | ||||||
| chr5:81335728
|
G | T | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1262+40C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335728 | ||||||
| chr5:81335962
|
A | G | 2 | a0001c0001t0002g0214a0001c0001t0005g0034 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1129-61T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81335962 | ||||||
| chr5:81335987
|
C | A | 5 | a0001c0001t0002g0214a0001c0001t0003g0194a0001c0001t0003g0237others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-86G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81335987 | ||||||
| chr5:81336036
|
CAT | C | 86 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(83): Show | 89 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1129-137_1129-136d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336036 | ||||||
| chr5:81336058
|
C | T | 7 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0003g0150others(4): Show | 8 | HG01167.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129-157G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336058 | ||||||
| chr5:81336096
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1129-195G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336096 | ||||||
| chr5:81336097
|
G | A | 1 | a0001c0001t0004g0025 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1129-196C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336097 | ||||||
| chr5:81336152
|
G | GT | 6 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0002g0002others(3): Show | 8 | HG00408.hp2 HG02027.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129-252dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336152 | ||||||
| chr5:81336163
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0002g0046others(1): Show | 4 | HG00438.hp2 NA18612.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-262A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336163 | ||||||
| chr5:81336244
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1129-343T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336244 | ||||||
| chr5:81336258
|
C | T | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-357G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336258 | ||||||
| chr5:81336360
|
G | C | 1 | a0001c0001t0002g0114 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1129-459C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336360 | ||||||
| chr5:81336394
|
C | G | 2 | a0002c0002t0001g0006a0002c0002t0003g0037 | 3 | HG01167.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1129-493G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336394 | ||||||
| chr5:81336430
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1129-529A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336430 | ||||||
| chr5:81336444
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0004g0148a0001c0001t0004g0161others(2): Show | 5 | HG01496.hp1 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-543C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336444 | ||||||
| chr5:81336474
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1129-573C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336474 | ||||||
| chr5:81336586
|
A | G | 1 | a0001c0001t0004g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1129-685T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336586 | ||||||
| chr5:81336714
|
T | C | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1129-813A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336714 | ||||||
| chr5:81336731
|
A | G | 5 | a0001c0001t0001g0042a0001c0001t0004g0148a0001c0001t0004g0161others(2): Show | 5 | HG01496.hp1 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-830T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336731 | ||||||
| chr5:81336849
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1129-948G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336849 | ||||||
| chr5:81336903
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1129-1002G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336903 | ||||||
| chr5:81336936
|
A | G | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1129-1035T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336936 | ||||||
| chr5:81337042
|
G | C | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-1141C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337042 | ||||||
| chr5:81337053
|
C | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1129-1152G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337053 | ||||||
| chr5:81337082
|
A | G | 7 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(4): Show | 7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-1181T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337082 | ||||||
| chr5:81337154
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0131 | 2 | HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1129-1253C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337154 | ||||||
| chr5:81337181
|
C | T | 61 | a0001c0001t0001g0109a0001c0001t0001g0131a0001c0001t0001g0195others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1129-1280G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337181 | ||||||
| chr5:81337218
|
T | G | 7 | a0002c0002t0001g0076a0002c0002t0002g0060a0002c0002t0002g0075others(4): Show | 7 | HG01106.hp2 HG01346.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129-1317A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337218 | ||||||
| chr5:81337255
|
G | A | 7 | a0001c0001t0002g0137a0001c0001t0003g0159a0001c0001t0003g0203others(4): Show | 7 | HG00741.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129-1354C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337255 | ||||||
| chr5:81337322
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1129-1421T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337322 | ||||||
| chr5:81337350
|
C | T | 1 | a0001c0001t0004g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1129-1449G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337350 | ||||||
| chr5:81337354
|
G | A | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1129-1453C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337354 | ||||||
| chr5:81337377
|
T | G | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-1476A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337377 | ||||||
| chr5:81337619
|
A | G | 5 | a0001c0001t0002g0214a0001c0001t0003g0194a0001c0001t0003g0237others(2): Show | 5 | HG02258.hp1 HG02486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-1718T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337619 | ||||||
| chr5:81337848
|
T | G | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-1947A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337848 | ||||||
| chr5:81337962
|
T | C | 7 | a0001c0001t0002g0137a0001c0001t0003g0159a0001c0001t0003g0203others(4): Show | 7 | HG00741.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129-2061A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337962 | ||||||
| chr5:81337977
|
A | G | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-2076T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337977 | ||||||
| chr5:81338043
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0004g0148a0001c0001t0005g0252 | 3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1129-2142G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338043 | ||||||
| chr5:81338150
|
T | C | 1 | a0001c0001t0002g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1129-2249A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338150 | ||||||
| chr5:81338161
|
A | G | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-2260T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338161 | ||||||
| chr5:81338293
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1129-2392G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338293 | ||||||
| chr5:81338496
|
G | A | 20 | a0002c0002t0001g0076a0002c0002t0001g0154a0002c0002t0002g0007others(17): Show | 21 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1129-2595C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338496 | ||||||
| chr5:81338644
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1129-2743G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338644 | ||||||
| chr5:81338893
|
A | C | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-2992T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338893 | ||||||
| chr5:81338946
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0002g0052a0001c0001t0002g0054 | 3 | HG02735.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1129-3045A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338946 | ||||||
| chr5:81339201
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-3300A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339201 | ||||||
| chr5:81339221
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-3320G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339221 | ||||||
| chr5:81339240
|
A | C | 61 | a0001c0001t0001g0109a0001c0001t0001g0131a0001c0001t0001g0195others(58): Show | 64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1129-3339T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339240 | ||||||
| chr5:81339300
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1128+3372G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339300 | ||||||
| chr5:81339683
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1128+2989G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339683 | ||||||
| chr5:81339716
|
A | G | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+2956T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339716 | ||||||
| chr5:81339800
|
C | T | 99 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(96): Show | 102 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1128+2872G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339800 | ||||||
| chr5:81339896
|
AT | A | 62 | a0001c0001t0001g0109a0001c0001t0001g0131a0001c0001t0001g0217others(59): Show | 64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1128+2775delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339896 | ||||||
| chr5:81339970
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1128+2702G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339970 | ||||||
| chr5:81340042
|
C | CT | 9 | a0001c0001t0001g0042a0001c0001t0002g0087a0001c0001t0002g0232others(6): Show | 9 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1128+2629dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340042 | ||||||
| chr5:81340042
|
C | CTT | 6 | a0001c0001t0002g0137a0001c0001t0003g0159a0001c0001t0003g0203others(3): Show | 6 | HG00741.hp2 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+2628_1128+262 others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340042 | ||||||
| chr5:81340060
|
T | A | 1 | a0001c0001t0004g0191 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1128+2612A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340060 | ||||||
| chr5:81340183
|
G | A | 16 | a0001c0001t0001g0196a0001c0001t0002g0041a0001c0001t0002g0197others(13): Show | 16 | HG02055.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1128+2489C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340183 | ||||||
| chr5:81340435
|
C | T | 4 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128+2237G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340435 | ||||||
| chr5:81340450
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+2222G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340450 | ||||||
| chr5:81340507
|
G | A | 4 | a0002c0002t0001g0154a0002c0002t0002g0040a0002c0002t0002g0209others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+2165C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340507 | ||||||
| chr5:81340508
|
C | T | 1 | a0001c0001t0004g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1128+2164G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340508 | ||||||
| chr5:81340653
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1128+2019G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340653 | ||||||
| chr5:81340717
|
G | A | 99 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(96): Show | 102 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1128+1955C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340717 | ||||||
| chr5:81340733
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1128+1939C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340733 | ||||||
| chr5:81340900
|
T | G | 1 | a0001c0001t0005g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1128+1772A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340900 | ||||||
| chr5:81341141
|
T | C | 4 | a0001c0001t0002g0214a0001c0001t0004g0161a0001c0001t0004g0162others(1): Show | 4 | HG01496.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+1531A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341141 | ||||||
| chr5:81341203
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1128+1469A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341203 | ||||||
| chr5:81341616
|
G | A | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+1056C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341616 | ||||||
| chr5:81341617
|
C | A | 2 | a0001c0001t0001g0081a0001c0001t0002g0093 | 2 | NA19081.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1128+1055G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341617 | ||||||
| chr5:81341652
|
T | C | 6 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(3): Show | 7 | HG01167.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+1020A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341652 | ||||||
| chr5:81341653
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0123 | 2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1128+1019C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341653 | ||||||
| chr5:81341710
|
G | A | 54 | a0001c0001t0001g0109a0001c0001t0001g0131a0001c0001t0001g0217others(51): Show | 56 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1128+962C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341710 | ||||||
| chr5:81341712
|
T | C | 9 | a0001c0001t0002g0041a0001c0001t0003g0017a0001c0001t0003g0145others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1128+960A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341712 | ||||||
| chr5:81341894
|
T | C | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+778A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341894 | ||||||
| chr5:81341999
|
A | AT | 7 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(4): Show | 7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+672dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341999 | ||||||
| chr5:81341999
|
A | T | 2 | a0001c0001t0002g0137a0001c0001t0003g0203 | 2 | HG00741.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1128+673T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341999 | ||||||
| chr5:81342002
|
T | TATTA | 7 | a0001c0001t0001g0042a0001c0001t0002g0232a0001c0001t0003g0018others(4): Show | 7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+669_1128+670i others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342002 | ||||||
| chr5:81342037
|
C | A | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+635G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342037 | ||||||
| chr5:81342286
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1128+386G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342286 | ||||||
| chr5:81342439
|
C | T | 4 | a0001c0001t0002g0232a0001c0001t0003g0018a0001c0001t0003g0022others(1): Show | 4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+233G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342439 | ||||||
| chr5:81342474
|
T | C | 1 | a0001c0007t0004g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1128+198A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342474 | ||||||
| chr5:81342772
|
A | G | 1 | a0001c0001t0003g0240 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1045-17T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81342772 | ||||||
| chr5:81342790
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1045-35C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81342790 | ||||||
| chr5:81342934
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1045-179G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81342934 | ||||||
| chr5:81343143
|
C | T | 1 | a0005c0006t0002g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1045-388G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343143 | ||||||
| chr5:81343144
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 6 | HG00609.hp2 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-389C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343144 | ||||||
| chr5:81343197
|
C | CA | 6 | a0001c0001t0001g0066a0001c0001t0001g0106a0001c0001t0003g0145others(3): Show | 6 | HG00621.hp2 HG01175.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-443dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343197 | ||||||
| chr5:81343207
|
C | A | 1 | a0001c0001t0003g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1045-452G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343207 | ||||||
| chr5:81343209
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1045-454G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343209 | ||||||
| chr5:81343246
|
A | C | 3 | a0001c0001t0001g0042a0001c0001t0004g0148a0001c0001t0005g0252 | 3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1045-491T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343246 | ||||||
| chr5:81343533
|
G | A | 6 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(3): Show | 7 | HG01167.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044+285C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343533 | ||||||
| chr5:81343682
|
T | C | 56 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0086others(53): Show | 60 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1044+136A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343682 | ||||||
| chr5:81343687
|
A | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1044+131T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343687 | ||||||
| chr5:81343691
|
C | T | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0001c0007t0004g0036 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1044+127G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343691 | ||||||
| chr5:81344314
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0004g0025 | 2 | HG02895.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.925-99C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344314 | ||||||
| chr5:81344406
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.925-191C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344406 | ||||||
| chr5:81344580
|
C | T | 8 | a0001c0001t0002g0041a0001c0001t0003g0017a0001c0001t0003g0150others(5): Show | 8 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.924+311G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344580 | ||||||
| chr5:81344727
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0004g0148a0001c0001t0005g0252 | 3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.924+164G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344727 | ||||||
| chr5:81344803
|
A | C | 7 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(4): Show | 7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+88T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344803 | ||||||
| chr5:81344817
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.924+74G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344817 | ||||||
| chr5:81345064
|
G | T | 29 | a0001c0001t0001g0042a0001c0001t0001g0196a0001c0001t0002g0041others(26): Show | 30 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.774-23C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345064 | ||||||
| chr5:81345093
|
CCCTCCTT others(14): Show |
C | 1 | a0001c0007t0004g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.774-73_774-53delTG others(19): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345093 | ||||||
| chr5:81345100
|
TGCACACC others(14): Show |
T | 96 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(93): Show | 99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.774-80_774-60delGA others(19): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345100 | ||||||
| chr5:81345103
|
ACACCGCT others(14): Show |
A | 1 | a0001c0001t0003g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774-83_774-63delGG others(19): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345103 | ||||||
| chr5:81345111
|
GCCACCTC others(5): Show |
G | 2 | a0001c0001t0003g0250a0001c0001t0004g0253 | 2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.774-82_774-71delGC others(10): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345111 | ||||||
| chr5:81345128
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0002g0214a0001c0001t0004g0148others(2): Show | 5 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-87G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345128 | ||||||
| chr5:81345129
|
G | A | 3 | a0001c0001t0003g0147a0001c0001t0004g0161a0001c0001t0004g0162 | 3 | HG01496.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.774-88C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345129 | ||||||
| chr5:81345153
|
G | T | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0001c0007t0004g0036 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.774-112C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345153 | ||||||
| chr5:81345347
|
G | A | 4 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.774-306C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345347 | ||||||
| chr5:81345362
|
A | T | 9 | a0001c0001t0003g0145a0001c0001t0003g0159a0001c0001t0003g0194others(6): Show | 9 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.774-321T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345362 | ||||||
| chr5:81345526
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.773+359A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345526 | ||||||
| chr5:81345652
|
A | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0102others(1): Show | 4 | NA18965.hp2 NA18971.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+233T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345652 | ||||||
| chr5:81345663
|
C | T | 3 | a0001c0001t0002g0214a0001c0001t0005g0034a0001c0005t0003g0202 | 3 | HG02258.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.773+222G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345663 | ||||||
| chr5:81345790
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0004g0148a0001c0001t0005g0252 | 3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.773+95G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345790 | ||||||
| chr5:81346039
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.654-35C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346039 | ||||||
| chr5:81346101
|
T | G | 5 | a0001c0001t0001g0195a0001c0001t0003g0020a0001c0001t0003g0149others(2): Show | 5 | HG02572.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-97A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346101 | ||||||
| chr5:81346396
|
T | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0195a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-392A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346396 | ||||||
| chr5:81346424
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.654-420G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346424 | ||||||
| chr5:81346438
|
G | A | 1 | a0001c0001t0004g0185 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.654-434C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346438 | ||||||
| chr5:81346475
|
A | G | 2 | a0001c0001t0002g0085a0001c0001t0002g0094 | 2 | NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.654-471T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346475 | ||||||
| chr5:81346506
|
A | G | 8 | a0001c0001t0001g0042a0001c0001t0001g0195a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-502T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346506 | ||||||
| chr5:81346694
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.654-690G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346694 | ||||||
| chr5:81346785
|
CTA | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0195a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-783_654-782del others(2): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346785 | ||||||
| chr5:81346874
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.654-870A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346874 | ||||||
| chr5:81346903
|
A | G | 7 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(4): Show | 7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+871T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346903 | ||||||
| chr5:81346917
|
G | C | 3 | a0001c0001t0001g0063a0001c0001t0004g0164a0001c0001t0004g0172 | 3 | HG00673.hp2 NA18950.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.653+857C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346917 | ||||||
| chr5:81347019
|
C | T | 5 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+755G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347019 | ||||||
| chr5:81347020
|
T | C | 1 | a0001c0001t0004g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.653+754A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347020 | ||||||
| chr5:81347401
|
C | A | 98 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(95): Show | 101 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.653+373G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347401 | ||||||
| chr5:81347510
|
C | G | 20 | a0001c0001t0002g0232a0002c0002t0001g0076a0002c0002t0001g0154others(17): Show | 21 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.653+264G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347510 | ||||||
| chr5:81347729
|
C | G | 1 | a0001c0001t0001g0043 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.653+45G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347729 | ||||||
| chr5:81348003
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0001g0119a0001c0001t0001g0122others(6): Show | 9 | HG00597.hp2 HG01346.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-73C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348003 | ||||||
| chr5:81348019
|
C | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0195a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-89G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348019 | ||||||
| chr5:81348288
|
A | T | 1 | a0002c0002t0003g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.497-358T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348288 | ||||||
| chr5:81348355
|
A | G | 101 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0131others(98): Show | 104 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.497-425T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348355 | ||||||
| chr5:81348403
|
A | G | 2 | a0001c0001t0002g0214a0001c0001t0005g0034 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497-473T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348403 | ||||||
| chr5:81348456
|
A | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0195a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-526T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348456 | ||||||
| chr5:81348629
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0004g0148a0001c0001t0005g0252 | 3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.497-699T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348629 | ||||||
| chr5:81348689
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-759G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348689 | ||||||
| chr5:81348746
|
G | T | 1 | a0001c0001t0004g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.497-816C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348746 | ||||||
| chr5:81348764
|
A | G | 9 | a0001c0001t0002g0041a0001c0001t0003g0017a0001c0001t0003g0150others(6): Show | 9 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-834T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348764 | ||||||
| chr5:81348775
|
G | T | 7 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(4): Show | 7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-845C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348775 | ||||||
| chr5:81348815
|
C | T | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-885G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348815 | ||||||
| chr5:81348842
|
G | A | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0001c0007t0004g0036 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.497-912C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348842 | ||||||
| chr5:81348889
|
C | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0195a0001c0001t0003g0020others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-959G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348889 | ||||||
| chr5:81348900
|
A | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.497-970T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348900 | ||||||
| chr5:81349005
|
C | T | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-1075G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349005 | ||||||
| chr5:81349273
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1343C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349273 | ||||||
| chr5:81349317
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0002g0138 | 2 | NA18612.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.497-1387G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349317 | ||||||
| chr5:81349319
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0003g0246others(3): Show | 6 | HG01361.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-1389G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349319 | ||||||
| chr5:81349405
|
C | T | 9 | a0001c0001t0001g0195a0001c0001t0003g0020a0001c0001t0003g0149others(6): Show | 9 | HG01361.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-1475G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349405 | ||||||
| chr5:81349486
|
T | A | 3 | a0001c0001t0004g0148a0001c0001t0005g0252a0001c0005t0003g0202 | 3 | HG02451.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-1556A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349486 | ||||||
| chr5:81349528
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1598G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349528 | ||||||
| chr5:81349537
|
C | T | 8 | a0002c0002t0001g0141a0002c0002t0001g0154a0002c0002t0001g0180others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-1607G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349537 | ||||||
| chr5:81349541
|
C | A | 2 | a0001c0001t0002g0214a0001c0001t0005g0034 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497-1611G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349541 | ||||||
| chr5:81349642
|
T | C | 3 | a0001c0001t0002g0137a0001c0001t0003g0018a0001c0001t0003g0022 | 3 | HG00741.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.497-1712A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349642 | ||||||
| chr5:81349745
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.497-1815C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349745 | ||||||
| chr5:81349828
|
C | T | 5 | a0001c0001t0003g0020a0001c0001t0003g0239a0001c0001t0003g0248others(2): Show | 6 | HG01167.hp2 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-1898G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349828 | ||||||
| chr5:81350005
|
G | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-2075C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350005 | ||||||
| chr5:81350127
|
C | T | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-2197G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350127 | ||||||
| chr5:81350192
|
G | T | 11 | a0001c0001t0001g0057a0001c0001t0001g0086a0001c0001t0002g0087others(8): Show | 13 | HG00099.hp1 HG01123.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-2262C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350192 | ||||||
| chr5:81350257
|
A | G | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0001c0007t0004g0036 | 3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.497-2327T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350257 | ||||||
| chr5:81350291
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.497-2361A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350291 | ||||||
| chr5:81350306
|
T | C | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-2376A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350306 | ||||||
| chr5:81350567
|
G | A | 25 | a0001c0001t0001g0071a0001c0001t0001g0123a0001c0001t0001g0166others(22): Show | 27 | HG00408.hp1 HG00673.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-2637C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350567 | ||||||
| chr5:81350699
|
G | C | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-2769C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350699 | ||||||
| chr5:81350736
|
A | G | 2 | a0001c0001t0003g0022a0002c0002t0007g0211 | 2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497-2806T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350736 | ||||||
| chr5:81350839
|
G | A | 6 | a0001c0001t0002g0041a0001c0001t0003g0017a0001c0001t0003g0018others(3): Show | 6 | HG02055.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-2909C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350839 | ||||||
| chr5:81350846
|
C | A | 1 | a0001c0001t0003g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.497-2916G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350846 | ||||||
| chr5:81350957
|
G | C | 4 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-3027C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350957 | ||||||
| chr5:81351062
|
T | G | 1 | a0001c0001t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-3132A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351062 | ||||||
| chr5:81351305
|
C | T | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-3375G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351305 | ||||||
| chr5:81351326
|
A | G | 7 | a0001c0001t0004g0004a0001c0001t0004g0016a0001c0001t0004g0019others(4): Show | 8 | HG01109.hp2 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-3396T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351326 | ||||||
| chr5:81351365
|
T | C | 91 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(88): Show | 97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.497-3435A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351365 | ||||||
| chr5:81351678
|
C | T | 77 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(74): Show | 82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.497-3748G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351678 | ||||||
| chr5:81351864
|
C | T | 7 | a0001c0001t0001g0039a0001c0001t0001g0065a0001c0001t0001g0080others(4): Show | 7 | HG01074.hp1 HG01106.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-3934G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351864 | ||||||
| chr5:81351994
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.497-4064G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351994 | ||||||
| chr5:81352009
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.497-4079G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352009 | ||||||
| chr5:81352022
|
C | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-4092G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352022 | ||||||
| chr5:81352080
|
C | T | 2 | a0001c0001t0002g0214a0001c0001t0005g0034 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497-4150G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352080 | ||||||
| chr5:81352295
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0123 | 2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.497-4365A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352295 | ||||||
| chr5:81352297
|
T | C | 1 | a0001c0001t0004g0029 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.497-4367A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352297 | ||||||
| chr5:81352696
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-4766C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352696 | ||||||
| chr5:81352795
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.497-4865T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352795 | ||||||
| chr5:81352844
|
C | T | 54 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(51): Show | 57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.497-4914G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352844 | ||||||
| chr5:81352876
|
G | A | 113 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(110): Show | 119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-4946C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352876 | ||||||
| chr5:81352961
|
T | C | 4 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-5031A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352961 | ||||||
| chr5:81353054
|
T | C | 22 | a0001c0001t0002g0077a0001c0001t0002g0108a0001c0001t0002g0206others(19): Show | 24 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-5124A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353054 | ||||||
| chr5:81353091
|
C | T | 17 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(14): Show | 17 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-5161G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353091 | ||||||
| chr5:81353186
|
G | A | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-5256C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353186 | ||||||
| chr5:81353255
|
G | A | 22 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(19): Show | 22 | HG00741.hp2 HG01884.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-5325C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353255 | ||||||
| chr5:81353293
|
GA | G | 3 | a0001c0001t0003g0022a0002c0002t0007g0211a0004c0004t0002g0220 | 3 | HG01361.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497-5364delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353293 | ||||||
| chr5:81353306
|
T | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5376A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353306 | ||||||
| chr5:81353307
|
T | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5377A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353307 | ||||||
| chr5:81353308
|
T | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5378A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353308 | ||||||
| chr5:81353309
|
T | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5379A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353309 | ||||||
| chr5:81353444
|
C | T | 39 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0001g0086others(36): Show | 42 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.497-5514G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353444 | ||||||
| chr5:81353579
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0123 | 2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.497-5649A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353579 | ||||||
| chr5:81353625
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0139 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.497-5695G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353625 | ||||||
| chr5:81353677
|
C | T | 8 | a0001c0001t0003g0020a0001c0001t0003g0147a0001c0001t0003g0239others(5): Show | 9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-5747G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353677 | ||||||
| chr5:81353802
|
A | G | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-5872T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353802 | ||||||
| chr5:81353996
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+5907G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353996 | ||||||
| chr5:81354047
|
T | A | 27 | a0001c0001t0001g0109a0001c0001t0001g0217a0001c0001t0001g0219others(24): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+5856A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354047 | ||||||
| chr5:81354062
|
C | A | 8 | a0001c0001t0003g0020a0001c0001t0003g0147a0001c0001t0003g0239others(5): Show | 9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+5841G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354062 | ||||||
| chr5:81354099
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.496+5804G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354099 | ||||||
| chr5:81354198
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.496+5705A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354198 | ||||||
| chr5:81354229
|
T | A | 90 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(87): Show | 96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.496+5674A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354229 | ||||||
| chr5:81354283
|
A | C | 1 | a0001c0001t0003g0240 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.496+5620T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354283 | ||||||
| chr5:81354328
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.496+5575C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354328 | ||||||
| chr5:81354367
|
T | C | 114 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(111): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.496+5536A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354367 | ||||||
| chr5:81354378
|
G | A | 89 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(86): Show | 95 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.496+5525C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354378 | ||||||
| chr5:81354595
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.496+5308T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354595 | ||||||
| chr5:81354643
|
C | T | 92 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(89): Show | 98 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.496+5260G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354643 | ||||||
| chr5:81354704
|
C | CT | 74 | a0001c0001t0001g0042a0001c0001t0001g0109a0001c0001t0001g0195others(71): Show | 79 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.496+5198dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354704 | ||||||
| chr5:81354825
|
T | A | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+5078A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354825 | ||||||
| chr5:81354912
|
G | A | 2 | a0001c0001t0004g0148a0001c0001t0005g0252 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.496+4991C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354912 | ||||||
| chr5:81354943
|
C | T | 1 | a0001c0001t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+4960G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354943 | ||||||
| chr5:81355071
|
G | T | 114 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(111): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.496+4832C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355071 | ||||||
| chr5:81355183
|
T | C | 8 | a0001c0001t0003g0020a0001c0001t0003g0147a0001c0001t0003g0239others(5): Show | 9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+4720A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355183 | ||||||
| chr5:81355264
|
C | T | 5 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+4639G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355264 | ||||||
| chr5:81355368
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.496+4535C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355368 | ||||||
| chr5:81355490
|
A | G | 84 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(81): Show | 90 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.496+4413T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355490 | ||||||
| chr5:81355515
|
A | G | 19 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(16): Show | 19 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+4388T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355515 | ||||||
| chr5:81355556
|
C | A | 19 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(16): Show | 19 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+4347G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355556 | ||||||
| chr5:81355751
|
T | G | 26 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(23): Show | 26 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+4152A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355751 | ||||||
| chr5:81355896
|
A | C | 19 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(16): Show | 19 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+4007T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355896 | ||||||
| chr5:81356010
|
C | T | 54 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(51): Show | 57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.496+3893G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356010 | ||||||
| chr5:81356034
|
G | A | 20 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(17): Show | 20 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.496+3869C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356034 | ||||||
| chr5:81356124
|
A | G | 5 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+3779T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356124 | ||||||
| chr5:81356225
|
C | T | 1 | a0001c0001t0003g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.496+3678G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356225 | ||||||
| chr5:81356272
|
A | G | 28 | a0001c0001t0001g0196a0001c0001t0002g0137a0001c0001t0002g0197others(25): Show | 29 | HG00741.hp2 HG01167.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+3631T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356272 | ||||||
| chr5:81356331
|
C | T | 27 | a0001c0001t0001g0195a0001c0001t0002g0077a0001c0001t0002g0108others(24): Show | 29 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+3572G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356331 | ||||||
| chr5:81356336
|
C | T | 53 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(50): Show | 56 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.496+3567G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356336 | ||||||
| chr5:81356511
|
C | T | 50 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(47): Show | 53 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.496+3392G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356511 | ||||||
| chr5:81356512
|
A | G | 50 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(47): Show | 53 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.496+3391T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356512 | ||||||
| chr5:81356596
|
C | G | 2 | a0001c0001t0002g0214a0001c0001t0005g0034 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.496+3307G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356596 | ||||||
| chr5:81356628
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.496+3275C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356628 | ||||||
| chr5:81356644
|
A | T | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+3259T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356644 | ||||||
| chr5:81356645
|
T | C | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+3258A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356645 | ||||||
| chr5:81356648
|
A | G | 1 | a0001c0001t0004g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.496+3255T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356648 | ||||||
| chr5:81356661
|
A | G | 5 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+3242T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356661 | ||||||
| chr5:81356749
|
C | T | 5 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(2): Show | 5 | HG01361.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+3154G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356749 | ||||||
| chr5:81356854
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.496+3049G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356854 | ||||||
| chr5:81356937
|
C | T | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.496+2966G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356937 | ||||||
| chr5:81356973
|
A | G | 50 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(47): Show | 53 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.496+2930T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356973 | ||||||
| chr5:81357137
|
C | T | 5 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(2): Show | 5 | HG01361.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+2766G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357137 | ||||||
| chr5:81357195
|
A | G | 8 | a0001c0001t0003g0020a0001c0001t0003g0147a0001c0001t0003g0239others(5): Show | 9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+2708T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357195 | ||||||
| chr5:81357380
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.496+2523C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357380 | ||||||
| chr5:81357413
|
T | A | 1 | a0001c0001t0002g0216 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.496+2490A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357413 | ||||||
| chr5:81357503
|
C | T | 52 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(49): Show | 55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+2400G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357503 | ||||||
| chr5:81357522
|
C | T | 1 | a0001c0001t0004g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.496+2381G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357522 | ||||||
| chr5:81357641
|
C | T | 52 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(49): Show | 55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+2262G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357641 | ||||||
| chr5:81357734
|
G | A | 41 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(38): Show | 44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.496+2169C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357734 | ||||||
| chr5:81357775
|
G | A | 4 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+2128C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357775 | ||||||
| chr5:81357780
|
C | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+2123G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357780 | ||||||
| chr5:81357781
|
G | A | 40 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(37): Show | 43 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.496+2122C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357781 | ||||||
| chr5:81357827
|
G | A | 1 | a0001c0001t0003g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+2076C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357827 | ||||||
| chr5:81357839
|
C | A | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+2064G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357839 | ||||||
| chr5:81357971
|
A | C | 1 | a0001c0001t0003g0203 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.496+1932T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357971 | ||||||
| chr5:81358007
|
C | CA | 25 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0106others(22): Show | 25 | HG00140.hp2 HG00438.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.496+1895dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358007 | ||||||
| chr5:81358007
|
CA | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0123a0001c0001t0001g0136others(3): Show | 6 | HG01069.hp2 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+1895delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358007 | ||||||
| chr5:81358007
|
CAAAAA | C | 47 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(44): Show | 50 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.496+1891_496+1895d others(7): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358007 | ||||||
| chr5:81358043
|
A | G | 52 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(49): Show | 55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+1860T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358043 | ||||||
| chr5:81358046
|
C | G | 52 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(49): Show | 55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+1857G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358046 | ||||||
| chr5:81358049
|
C | G | 52 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(49): Show | 55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+1854G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358049 | ||||||
| chr5:81358050
|
T | C | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+1853A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358050 | ||||||
| chr5:81358136
|
T | A | 41 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(38): Show | 44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.496+1767A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358136 | ||||||
| chr5:81358357
|
G | C | 8 | a0001c0001t0003g0020a0001c0001t0003g0147a0001c0001t0003g0239others(5): Show | 9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+1546C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358357 | ||||||
| chr5:81358388
|
T | C | 1 | a0001c0001t0003g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.496+1515A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358388 | ||||||
| chr5:81358453
|
C | A | 41 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(38): Show | 44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.496+1450G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358453 | ||||||
| chr5:81358693
|
T | C | 5 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+1210A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358693 | ||||||
| chr5:81358709
|
C | T | 5 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+1194G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358709 | ||||||
| chr5:81358782
|
T | C | 15 | a0001c0001t0001g0195a0001c0001t0002g0137a0001c0001t0002g0210others(12): Show | 15 | HG00741.hp2 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+1121A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358782 | ||||||
| chr5:81358798
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.496+1105C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358798 | ||||||
| chr5:81358838
|
A | G | 1 | a0001c0001t0004g0167 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496+1065T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358838 | ||||||
| chr5:81358853
|
G | GA | 18 | a0001c0001t0001g0195a0001c0001t0002g0137a0001c0001t0002g0210others(15): Show | 18 | HG00741.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.496+1049dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358853 | ||||||
| chr5:81358853
|
GA | G | 7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0117others(4): Show | 7 | HG01943.hp2 HG01975.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+1049delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358853 | ||||||
| chr5:81358853
|
GAA | G | 42 | a0001c0001t0001g0196a0001c0001t0002g0077a0001c0001t0002g0108others(39): Show | 45 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.496+1048_496+1049d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358853 | ||||||
| chr5:81359051
|
A | C | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+852T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359051 | ||||||
| chr5:81359147
|
T | G | 217 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0042others(214): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.496+756A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359147 | ||||||
| chr5:81359242
|
C | T | 2 | a0001c0001t0004g0016a0001c0001t0004g0021 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.496+661G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359242 | ||||||
| chr5:81359304
|
C | T | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+599G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359304 | ||||||
| chr5:81359317
|
T | C | 4 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(1): Show | 4 | HG01884.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+586A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359317 | ||||||
| chr5:81359325
|
C | A | 8 | a0001c0001t0003g0020a0001c0001t0003g0181a0001c0001t0003g0182others(5): Show | 9 | HG01167.hp2 HG01168.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+578G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359325 | ||||||
| chr5:81359369
|
C | T | 1 | a0002c0002t0003g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496+534G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359369 | ||||||
| chr5:81359443
|
T | C | 2 | a0001c0001t0004g0016a0001c0001t0004g0021 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.496+460A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359443 | ||||||
| chr5:81359447
|
T | C | 116 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0109others(113): Show | 122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.496+456A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359447 | ||||||
| chr5:81359687
|
T | G | 1 | a0001c0001t0002g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.496+216A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359687 | ||||||
| chr5:81359798
|
A | G | 1 | a0002c0002t0002g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.496+105T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359798 | ||||||
| chr5:81359890
|
T | C | 27 | a0001c0001t0001g0109a0001c0001t0001g0217a0001c0001t0001g0219others(24): Show | 29 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+13A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359890 | ||||||
| chr5:81360147
|
T | C | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.361-109A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360147 | ||||||
| chr5:81360225
|
A | T | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-187T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360225 | ||||||
| chr5:81360345
|
G | T | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-307C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360345 | ||||||
| chr5:81360393
|
C | CTTTGCAA others(29): Show |
1 | a0001c0001t0003g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.361-391_361-356dup others(36): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360393 | ||||||
| chr5:81360393
|
CTTTGCAA others(29): Show |
C | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-391_361-356del others(36): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360393 | ||||||
| chr5:81360525
|
G | C | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.361-487C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360525 | ||||||
| chr5:81360550
|
A | G | 1 | a0001c0001t0002g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-512T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360550 | ||||||
| chr5:81360595
|
A | C | 1 | a0002c0002t0003g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.361-557T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360595 | ||||||
| chr5:81360827
|
G | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0239a0001c0001t0003g0248others(1): Show | 5 | HG01167.hp2 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-789C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360827 | ||||||
| chr5:81360911
|
G | C | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-873C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360911 | ||||||
| chr5:81360934
|
C | T | 3 | a0002c0002t0001g0154a0002c0002t0002g0040a0002c0002t0004g0247 | 3 | HG01891.hp1 HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.361-896G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360934 | ||||||
| chr5:81360949
|
AC | A | 7 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(4): Show | 7 | HG02486.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-912delG | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360949 | ||||||
| chr5:81360992
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-954G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360992 | ||||||
| chr5:81360993
|
G | T | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-955C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360993 | ||||||
| chr5:81361077
|
C | CA | 82 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0083others(79): Show | 89 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.361-1040dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361077 | ||||||
| chr5:81361077
|
C | CAAAAAAA others(6): Show |
1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-1052_361-1040d others(15): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361077 | ||||||
| chr5:81361077
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0081a0001c0001t0001g0127a0001c0001t0002g0093others(1): Show | 4 | NA18612.hp1 NA18944.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-1053_361-1040d others(16): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361077 | ||||||
| chr5:81361103
|
A | G | 4 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-1065T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361103 | ||||||
| chr5:81361124
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.361-1086A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361124 | ||||||
| chr5:81361218
|
C | CTT | 22 | a0001c0001t0002g0077a0001c0001t0002g0108a0001c0001t0002g0206others(19): Show | 24 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.361-1182_361-1181d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361218 | ||||||
| chr5:81361258
|
G | C | 4 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(1): Show | 4 | HG01884.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-1220C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361258 | ||||||
| chr5:81361315
|
G | T | 28 | a0001c0001t0002g0077a0001c0001t0002g0108a0001c0001t0002g0206others(25): Show | 30 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.361-1277C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361315 | ||||||
| chr5:81361343
|
C | T | 1 | a0001c0001t0003g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.361-1305G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361343 | ||||||
| chr5:81361366
|
T | C | 2 | a0001c0001t0002g0214a0001c0001t0005g0034 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.361-1328A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361366 | ||||||
| chr5:81361417
|
T | G | 1 | a0001c0001t0004g0233 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.361-1379A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361417 | ||||||
| chr5:81361481
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.361-1443C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361481 | ||||||
| chr5:81361497
|
A | G | 1 | a0004c0004t0002g0220 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-1459T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361497 | ||||||
| chr5:81361511
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0004g0015a0002c0002t0007g0211 | 3 | HG02055.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.361-1473T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361511 | ||||||
| chr5:81361573
|
G | C | 1 | a0002c0002t0003g0037 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.361-1535C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361573 | ||||||
| chr5:81361580
|
G | C | 1 | a0001c0001t0004g0236 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.361-1542C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361580 | ||||||
| chr5:81361650
|
T | G | 3 | a0001c0001t0004g0148a0001c0001t0005g0252a0004c0004t0002g0220 | 3 | HG01361.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.361-1612A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361650 | ||||||
| chr5:81361740
|
T | C | 1 | a0001c0001t0001g0112 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.361-1702A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361740 | ||||||
| chr5:81361761
|
A | C | 6 | a0001c0001t0002g0041a0001c0001t0003g0017a0001c0001t0003g0018others(3): Show | 6 | HG02055.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-1723T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361761 | ||||||
| chr5:81361870
|
G | C | 129 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0086others(126): Show | 137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.361-1832C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361870 | ||||||
| chr5:81361910
|
T | C | 30 | a0001c0001t0001g0086a0001c0001t0001g0109a0001c0001t0001g0217others(27): Show | 32 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.361-1872A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361910 | ||||||
| chr5:81362163
|
CT | C | 40 | a0001c0001t0001g0071a0001c0001t0001g0086a0001c0001t0001g0121others(37): Show | 42 | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.360+1624delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362163 | ||||||
| chr5:81362163
|
CTT | C | 66 | a0001c0001t0001g0042a0001c0001t0001g0069a0001c0001t0001g0109others(63): Show | 70 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.360+1623_360+1624d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362163 | ||||||
| chr5:81362166
|
T | C | 14 | a0001c0001t0001g0039a0001c0001t0001g0057a0001c0001t0001g0110others(11): Show | 16 | HG00099.hp1 HG01069.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.360+1622A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362166 | ||||||
| chr5:81362172
|
T | C | 1 | a0001c0001t0004g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360+1616A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362172 | ||||||
| chr5:81362187
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.360+1601G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362187 | ||||||
| chr5:81362293
|
G | A | 1 | a0001c0001t0004g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360+1495C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362293 | ||||||
| chr5:81362306
|
T | C | 3 | a0001c0001t0002g0137a0001c0001t0003g0159a0001c0001t0004g0251 | 3 | HG00741.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.360+1482A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362306 | ||||||
| chr5:81362354
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.360+1434C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362354 | ||||||
| chr5:81362376
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.360+1412C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362376 | ||||||
| chr5:81362525
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.360+1263C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362525 | ||||||
| chr5:81362529
|
G | A | 4 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0144others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1259C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362529 | ||||||
| chr5:81362850
|
G | A | 2 | a0001c0001t0002g0210a0001c0001t0003g0145 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.360+938C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362850 | ||||||
| chr5:81362958
|
C | T | 7 | a0001c0001t0003g0254a0001c0001t0003g0256a0001c0001t0003g0257others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+830G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362958 | ||||||
| chr5:81363020
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.360+768T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363020 | ||||||
| chr5:81363078
|
T | G | 1 | a0001c0001t0002g0111 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.360+710A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363078 | ||||||
| chr5:81363247
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.360+541G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363247 | ||||||
| chr5:81363413
|
T | C | 1 | a0002c0002t0003g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.360+375A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363413 | ||||||
| chr5:81363429
|
G | T | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.360+359C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363429 | ||||||
| chr5:81363757
|
T | C | 5 | a0001c0001t0003g0157a0001c0001t0003g0234a0001c0001t0004g0161others(2): Show | 5 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+31A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363757 | ||||||
| chr5:81363919
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.259-30G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81363919 | ||||||
| chr5:81364158
|
C | T | 1 | a0001c0001t0004g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.259-269G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364158 | ||||||
| chr5:81364199
|
G | C | 1 | a0001c0001t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259-310C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364199 | ||||||
| chr5:81364239
|
A | C | 2 | a0001c0001t0004g0148a0001c0005t0003g0202 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-350T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364239 | ||||||
| chr5:81364287
|
C | T | 60 | a0001c0001t0001g0042a0001c0001t0001g0074a0001c0001t0001g0196others(57): Show | 63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.259-398G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364287 | ||||||
| chr5:81364581
|
C | T | 2 | a0001c0001t0003g0159a0001c0001t0004g0160 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.259-692G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364581 | ||||||
| chr5:81364621
|
A | C | 1 | a0001c0001t0003g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-732T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364621 | ||||||
| chr5:81364852
|
CT | C | 67 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0074others(64): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.259-964delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364852 | ||||||
| chr5:81364870
|
C | A | 14 | a0001c0001t0003g0003a0001c0001t0003g0239a0001c0001t0003g0240others(11): Show | 16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-981G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364870 | ||||||
| chr5:81364872
|
C | G | 19 | a0001c0001t0001g0166a0001c0001t0003g0165a0001c0001t0003g0168others(16): Show | 20 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.259-983G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364872 | ||||||
| chr5:81365126
|
T | C | 90 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0057others(87): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.259-1237A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365126 | ||||||
| chr5:81365149
|
A | G | 7 | a0001c0001t0003g0157a0001c0001t0003g0234a0001c0001t0004g0148others(4): Show | 7 | HG01496.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-1260T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365149 | ||||||
| chr5:81365215
|
A | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-1326T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365215 | ||||||
| chr5:81365231
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 6 | HG03098.hp2 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1342T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365231 | ||||||
| chr5:81365299
|
T | A | 7 | a0001c0001t0003g0157a0001c0001t0003g0234a0001c0001t0004g0148others(4): Show | 7 | HG01496.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-1410A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365299 | ||||||
| chr5:81365518
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.259-1629T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365518 | ||||||
| chr5:81365721
|
C | T | 5 | a0001c0001t0003g0157a0001c0001t0003g0234a0001c0001t0004g0161others(2): Show | 5 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1832G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365721 | ||||||
| chr5:81365742
|
G | A | 1 | a0001c0001t0003g0187 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-1853C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365742 | ||||||
| chr5:81365877
|
A | G | 162 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0057others(159): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.259-1988T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365877 | ||||||
| chr5:81365927
|
T | A | 1 | a0001c0001t0003g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.259-2038A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365927 | ||||||
| chr5:81366205
|
A | C | 1 | a0001c0001t0002g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.259-2316T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366205 | ||||||
| chr5:81366265
|
T | C | 1 | a0001c0001t0004g0015 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.259-2376A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366265 | ||||||
| chr5:81366324
|
A | C | 20 | a0001c0001t0001g0195a0001c0001t0002g0146a0001c0001t0003g0003others(17): Show | 22 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.259-2435T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366324 | ||||||
| chr5:81366435
|
A | G | 21 | a0001c0001t0001g0166a0001c0001t0003g0165a0001c0001t0003g0168others(18): Show | 22 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.259-2546T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366435 | ||||||
| chr5:81366582
|
C | A | 2 | a0001c0001t0003g0250a0001c0001t0004g0251 | 2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.259-2693G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366582 | ||||||
| chr5:81366609
|
A | C | 2 | a0001c0001t0003g0022a0001c0001t0005g0034 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.259-2720T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366609 | ||||||
| chr5:81366673
|
T | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0123 | 2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.259-2784A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366673 | ||||||
| chr5:81366742
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.259-2853T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366742 | ||||||
| chr5:81366770
|
A | T | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-2881T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366770 | ||||||
| chr5:81366827
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-2938T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366827 | ||||||
| chr5:81366869
|
G | A | 12 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0176others(9): Show | 13 | HG00609.hp1 HG01074.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-2980C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366869 | ||||||
| chr5:81366882
|
C | A | 5 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0004g0015others(2): Show | 5 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-2993G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366882 | ||||||
| chr5:81366895
|
T | G | 1 | a0001c0001t0003g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.259-3006A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366895 | ||||||
| chr5:81367291
|
T | A | 9 | a0001c0001t0001g0039a0001c0001t0001g0139a0001c0001t0002g0077others(6): Show | 9 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-3402A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367291 | ||||||
| chr5:81367490
|
A | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-3601T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367490 | ||||||
| chr5:81367551
|
T | C | 3 | a0001c0001t0003g0234a0001c0001t0004g0161a0001c0001t0004g0162 | 3 | HG01496.hp1 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.259-3662A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367551 | ||||||
| chr5:81367648
|
G | A | 27 | a0001c0001t0001g0166a0001c0001t0003g0152a0001c0001t0003g0165others(24): Show | 28 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.259-3759C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367648 | ||||||
| chr5:81367691
|
A | G | 63 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0074others(60): Show | 67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.259-3802T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367691 | ||||||
| chr5:81367711
|
C | T | 1 | a0001c0001t0002g0089 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.259-3822G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367711 | ||||||
| chr5:81367724
|
T | C | 4 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-3835A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367724 | ||||||
| chr5:81367736
|
T | C | 2 | a0001c0001t0003g0014a0001c0001t0003g0203 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-3847A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367736 | ||||||
| chr5:81367828
|
A | T | 3 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0158 | 3 | HG02572.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.258+3922T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367828 | ||||||
| chr5:81367919
|
A | G | 23 | a0001c0001t0001g0166a0001c0001t0003g0152a0001c0001t0003g0165others(20): Show | 24 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.258+3831T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367919 | ||||||
| chr5:81367948
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.258+3802C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367948 | ||||||
| chr5:81368016
|
G | T | 6 | a0001c0001t0003g0157a0001c0001t0003g0234a0001c0001t0004g0161others(3): Show | 6 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+3734C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368016 | ||||||
| chr5:81368044
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258+3706G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368044 | ||||||
| chr5:81368247
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.258+3503C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368247 | ||||||
| chr5:81368583
|
A | G | 3 | a0001c0001t0003g0157a0001c0001t0004g0193a0001c0001t0005g0144 | 3 | HG06807.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+3167T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368583 | ||||||
| chr5:81368745
|
A | G | 1 | a0001c0001t0003g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.258+3005T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368745 | ||||||
| chr5:81368781
|
TAGAATG | T | 4 | a0001c0001t0003g0022a0001c0001t0005g0034a0002c0002t0002g0209others(1): Show | 4 | HG02896.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+2963_258+2968d others(8): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368781 | ||||||
| chr5:81369002
|
G | A | 70 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0074others(67): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.258+2748C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369002 | ||||||
| chr5:81369047
|
T | C | 1 | a0001c0001t0003g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.258+2703A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369047 | ||||||
| chr5:81369154
|
C | CA | 14 | a0001c0001t0001g0069a0001c0001t0003g0022a0001c0001t0003g0239others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+2595dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369154 | ||||||
| chr5:81369154
|
CA | C | 12 | a0001c0001t0001g0074a0001c0001t0002g0124a0001c0001t0002g0125others(9): Show | 12 | HG00140.hp1 HG01192.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.258+2595delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369154 | ||||||
| chr5:81369311
|
G | C | 89 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0057others(86): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.258+2439C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369311 | ||||||
| chr5:81369312
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.258+2438T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369312 | ||||||
| chr5:81369378
|
C | T | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.258+2372G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369378 | ||||||
| chr5:81369439
|
T | A | 4 | a0001c0001t0001g0196a0001c0001t0002g0197a0001c0001t0002g0204others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+2311A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369439 | ||||||
| chr5:81369549
|
C | T | 23 | a0001c0001t0001g0166a0001c0001t0003g0152a0001c0001t0003g0165others(20): Show | 24 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.258+2201G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369549 | ||||||
| chr5:81369552
|
C | A | 2 | a0001c0001t0003g0159a0001c0001t0004g0160 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.258+2198G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369552 | ||||||
| chr5:81369552
|
C | T | 20 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0086others(17): Show | 21 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.258+2198G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369552 | ||||||
| chr5:81369559
|
A | G | 1 | a0001c0001t0002g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.258+2191T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369559 | ||||||
| chr5:81369597
|
G | A | 3 | a0001c0001t0003g0157a0001c0001t0004g0148a0001c0005t0003g0202 | 3 | HG02451.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.258+2153C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369597 | ||||||
| chr5:81369730
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.258+2020G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369730 | ||||||
| chr5:81369773
|
T | A | 13 | a0001c0001t0003g0003a0001c0001t0003g0239a0001c0001t0003g0240others(10): Show | 15 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+1977A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369773 | ||||||
| chr5:81369881
|
C | T | 68 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(65): Show | 72 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.258+1869G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369881 | ||||||
| chr5:81369953
|
T | C | 3 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207 | 3 | HG01884.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.258+1797A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369953 | ||||||
| chr5:81370010
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.258+1740T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370010 | ||||||
| chr5:81370016
|
C | T | 74 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0074others(71): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.258+1734G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370016 | ||||||
| chr5:81370032
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.258+1718A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370032 | ||||||
| chr5:81370144
|
T | C | 4 | a0001c0001t0003g0176a0001c0001t0003g0234a0001c0001t0004g0161others(1): Show | 4 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+1606A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370144 | ||||||
| chr5:81370144
|
T | G | 13 | a0001c0001t0002g0137a0001c0001t0003g0003a0001c0001t0003g0239others(10): Show | 15 | HG00741.hp2 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.258+1606A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370144 | ||||||
| chr5:81370395
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.258+1355T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370395 | ||||||
| chr5:81370564
|
G | A | 1 | a0001c0001t0003g0176 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.258+1186C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370564 | ||||||
| chr5:81370649
|
A | G | 158 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(155): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.258+1101T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370649 | ||||||
| chr5:81370698
|
T | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0212a0001c0001t0001g0213 | 4 | NA18957.hp1 NA18961.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1052A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370698 | ||||||
| chr5:81370775
|
C | A | 1 | a0001c0001t0002g0114 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.258+975G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370775 | ||||||
| chr5:81370820
|
C | G | 1 | a0001c0001t0004g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.258+930G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370820 | ||||||
| chr5:81370840
|
G | C | 1 | a0001c0001t0004g0169 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.258+910C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370840 | ||||||
| chr5:81370846
|
G | A | 1 | a0001c0001t0004g0253 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+904C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370846 | ||||||
| chr5:81370914
|
G | A | 124 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(121): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.258+836C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370914 | ||||||
| chr5:81370919
|
T | A | 1 | a0002c0002t0001g0180 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258+831A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370919 | ||||||
| chr5:81371059
|
T | C | 2 | a0001c0001t0001g0039a0001c0001t0001g0139 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.258+691A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371059 | ||||||
| chr5:81371097
|
G | A | 7 | a0001c0001t0003g0031a0001c0001t0004g0005a0001c0001t0004g0024others(4): Show | 8 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+653C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371097 | ||||||
| chr5:81371361
|
G | A | 9 | a0001c0001t0001g0195a0001c0001t0002g0146a0001c0001t0002g0210others(6): Show | 9 | HG02451.hp1 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+389C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371361 | ||||||
| chr5:81371418
|
A | AT | 5 | a0001c0001t0001g0012a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 6 | HG03098.hp2 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+331dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371418 | ||||||
| chr5:81371418
|
AT | A | 26 | a0001c0001t0002g0214a0001c0001t0003g0017a0001c0001t0003g0018others(23): Show | 28 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.258+331delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371418 | ||||||
| chr5:81371515
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0084 | 2 | NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.258+235T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371515 | ||||||
| chr5:81371551
|
C | T | 3 | a0001c0001t0003g0184a0001c0001t0003g0188a0001c0001t0003g0190 | 3 | HG01346.hp2 HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.258+199G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371551 | ||||||
| chr5:81371688
|
C | T | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.258+62G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371688 | ||||||
| chr5:81371853
|
T | C | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198-43A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371853 | ||||||
| chr5:81371873
|
A | G | 4 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-63T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371873 | ||||||
| chr5:81371919
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02135.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.198-109G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371919 | ||||||
| chr5:81371938
|
C | G | 125 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(122): Show | 132 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.198-128G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371938 | ||||||
| chr5:81372085
|
G | A | 1 | a0001c0001t0004g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.198-275C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372085 | ||||||
| chr5:81372096
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198-286G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372096 | ||||||
| chr5:81372306
|
C | T | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0002c0002t0007g0211 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.198-496G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372306 | ||||||
| chr5:81372329
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.198-519G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372329 | ||||||
| chr5:81372402
|
A | G | 30 | a0001c0001t0001g0166a0001c0001t0001g0195a0001c0001t0002g0146others(27): Show | 30 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.198-592T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372402 | ||||||
| chr5:81372426
|
C | T | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.198-616G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372426 | ||||||
| chr5:81372589
|
T | C | 32 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(29): Show | 34 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.198-779A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372589 | ||||||
| chr5:81372662
|
C | T | 30 | a0001c0001t0001g0166a0001c0001t0001g0195a0001c0001t0002g0146others(27): Show | 30 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.198-852G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372662 | ||||||
| chr5:81372748
|
T | C | 1 | a0003c0003t0001g0009 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.198-938A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372748 | ||||||
| chr5:81372903
|
T | C | 1 | a0001c0001t0002g0070 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.198-1093A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372903 | ||||||
| chr5:81372913
|
C | T | 23 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(20): Show | 25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.198-1103G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372913 | ||||||
| chr5:81373082
|
G | A | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198-1272C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373082 | ||||||
| chr5:81373085
|
C | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(33): Show | 38 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-1275G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373085 | ||||||
| chr5:81373156
|
A | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(33): Show | 38 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-1346T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373156 | ||||||
| chr5:81373193
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.198-1383G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373193 | ||||||
| chr5:81373432
|
C | G | 26 | a0001c0001t0002g0214a0001c0001t0003g0017a0001c0001t0003g0018others(23): Show | 28 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.198-1622G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373432 | ||||||
| chr5:81373438
|
G | A | 3 | a0001c0001t0002g0115a0001c0001t0002g0128a0001c0001t0002g0129 | 3 | HG00642.hp1 HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.198-1628C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373438 | ||||||
| chr5:81373540
|
G | A | 3 | a0001c0001t0003g0159a0001c0001t0003g0234a0001c0001t0004g0160 | 3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.198-1730C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373540 | ||||||
| chr5:81373560
|
G | A | 1 | a0002c0002t0002g0058 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.198-1750C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373560 | ||||||
| chr5:81373586
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.198-1776C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373586 | ||||||
| chr5:81373741
|
C | A | 11 | a0001c0001t0003g0010a0001c0001t0003g0184a0001c0001t0003g0186others(8): Show | 12 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.198-1931G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373741 | ||||||
| chr5:81373748
|
A | C | 1 | a0001c0001t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.198-1938T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373748 | ||||||
| chr5:81373904
|
C | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(15): Show | 19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-2094G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373904 | ||||||
| chr5:81373922
|
A | T | 6 | a0001c0001t0003g0022a0001c0001t0003g0159a0001c0001t0003g0234others(3): Show | 6 | HG02615.hp1 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-2112T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373922 | ||||||
| chr5:81374240
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.198-2430T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374240 | ||||||
| chr5:81374245
|
G | A | 1 | a0001c0001t0003g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198-2435C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374245 | ||||||
| chr5:81374392
|
G | A | 30 | a0001c0001t0001g0166a0001c0001t0001g0195a0001c0001t0002g0146others(27): Show | 30 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.198-2582C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374392 | ||||||
| chr5:81374499
|
T | C | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0002c0002t0007g0211 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.198-2689A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374499 | ||||||
| chr5:81374686
|
A | T | 23 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(20): Show | 25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.198-2876T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374686 | ||||||
| chr5:81374838
|
A | T | 22 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.198-3028T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374838 | ||||||
| chr5:81374922
|
A | T | 1 | a0001c0001t0002g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.198-3112T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374922 | ||||||
| chr5:81375080
|
G | A | 159 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0057others(156): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.198-3270C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375080 | ||||||
| chr5:81375135
|
C | T | 13 | a0001c0001t0003g0010a0001c0001t0003g0184a0001c0001t0003g0186others(10): Show | 14 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.198-3325G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375135 | ||||||
| chr5:81375176
|
C | G | 159 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0057others(156): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.198-3366G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375176 | ||||||
| chr5:81375205
|
G | C | 18 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(15): Show | 19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-3395C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375205 | ||||||
| chr5:81375468
|
C | G | 7 | a0001c0001t0003g0031a0001c0001t0004g0005a0001c0001t0004g0024others(4): Show | 8 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-3658G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375468 | ||||||
| chr5:81375566
|
T | C | 92 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(89): Show | 98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.198-3756A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375566 | ||||||
| chr5:81375601
|
T | C | 3 | a0001c0001t0003g0022a0001c0001t0005g0034a0002c0002t0003g0037 | 3 | HG03139.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.198-3791A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375601 | ||||||
| chr5:81375674
|
A | G | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198-3864T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375674 | ||||||
| chr5:81376036
|
ATTC | A | 4 | a0002c0002t0001g0141a0002c0002t0001g0180a0002c0002t0002g0207others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-4229_198-4227d others(5): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376036 | ||||||
| chr5:81376147
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0239a0001c0001t0003g0240others(11): Show | 16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.198-4337G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376147 | ||||||
| chr5:81376460
|
G | A | 2 | a0001c0001t0003g0031a0001c0001t0004g0032 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.198-4650C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376460 | ||||||
| chr5:81376478
|
ATAAC | A | 18 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(15): Show | 19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-4672_198-4669d others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376478 | ||||||
| chr5:81376623
|
C | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(15): Show | 19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-4813G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376623 | ||||||
| chr5:81376701
|
C | A | 17 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(14): Show | 18 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.198-4891G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376701 | ||||||
| chr5:81376746
|
G | T | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198-4936C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376746 | ||||||
| chr5:81376894
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198-5084C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376894 | ||||||
| chr5:81377107
|
C | A | 18 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(15): Show | 19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-5297G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377107 | ||||||
| chr5:81377107
|
C | T | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.198-5297G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377107 | ||||||
| chr5:81377289
|
A | G | 158 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(155): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.198-5479T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377289 | ||||||
| chr5:81377497
|
C | T | 14 | a0001c0001t0003g0003a0001c0001t0003g0239a0001c0001t0003g0240others(11): Show | 16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.198-5687G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377497 | ||||||
| chr5:81377647
|
A | G | 23 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(20): Show | 25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.198-5837T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377647 | ||||||
| chr5:81377677
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.198-5867C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377677 | ||||||
| chr5:81377835
|
C | T | 128 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(125): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.198-6025G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377835 | ||||||
| chr5:81377860
|
T | A | 1 | a0001c0001t0003g0188 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.198-6050A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377860 | ||||||
| chr5:81377874
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.198-6064T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377874 | ||||||
| chr5:81377955
|
T | A | 74 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(71): Show | 79 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.198-6145A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377955 | ||||||
| chr5:81378049
|
T | C | 92 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(89): Show | 98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.198-6239A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378049 | ||||||
| chr5:81378246
|
T | C | 1 | a0001c0001t0003g0189 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.198-6436A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378246 | ||||||
| chr5:81378261
|
G | A | 14 | a0001c0001t0003g0003a0001c0001t0003g0239a0001c0001t0003g0240others(11): Show | 16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.198-6451C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378261 | ||||||
| chr5:81378320
|
T | C | 1 | a0001c0001t0003g0241 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.198-6510A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378320 | ||||||
| chr5:81378658
|
A | C | 1 | a0001c0001t0001g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.198-6848T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378658 | ||||||
| chr5:81378668
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.198-6858G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378668 | ||||||
| chr5:81378750
|
T | G | 7 | a0001c0001t0003g0174a0001c0001t0003g0175a0001c0001t0004g0164others(4): Show | 7 | HG00408.hp1 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-6940A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378750 | ||||||
| chr5:81379130
|
C | T | 21 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.197+6627G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379130 | ||||||
| chr5:81379178
|
C | T | 1 | a0002c0002t0003g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+6579G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379178 | ||||||
| chr5:81379184
|
C | T | 1 | a0001c0001t0004g0019 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.197+6573G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379184 | ||||||
| chr5:81379317
|
C | T | 18 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(15): Show | 19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+6440G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379317 | ||||||
| chr5:81379332
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.197+6425C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379332 | ||||||
| chr5:81379339
|
G | A | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197+6418C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379339 | ||||||
| chr5:81379499
|
C | T | 1 | a0002c0002t0003g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+6258G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379499 | ||||||
| chr5:81379534
|
C | T | 22 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.197+6223G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379534 | ||||||
| chr5:81379555
|
C | T | 1 | a0001c0001t0004g0023 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.197+6202G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379555 | ||||||
| chr5:81379578
|
C | T | 1 | a0005c0006t0002g0155 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197+6179G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379578 | ||||||
| chr5:81379622
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.197+6135A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379622 | ||||||
| chr5:81379677
|
G | A | 128 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(125): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.197+6080C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379677 | ||||||
| chr5:81379880
|
G | A | 18 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(15): Show | 19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+5877C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379880 | ||||||
| chr5:81380061
|
T | G | 2 | a0001c0001t0003g0250a0001c0001t0004g0251 | 2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.197+5696A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380061 | ||||||
| chr5:81380272
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.197+5485T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380272 | ||||||
| chr5:81380446
|
C | G | 1 | a0001c0001t0003g0145 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.197+5311G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380446 | ||||||
| chr5:81380519
|
G | C | 1 | a0001c0001t0002g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.197+5238C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380519 | ||||||
| chr5:81380527
|
G | GCACTT | 92 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(89): Show | 98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+5225_197+5229d others(7): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380527 | ||||||
| chr5:81380574
|
AAAAAAAG | A | 21 | a0001c0001t0001g0166a0001c0001t0003g0152a0001c0001t0003g0165others(18): Show | 21 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.197+5176_197+5182d others(9): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380574 | ||||||
| chr5:81380578
|
A | G | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197+5179T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380578 | ||||||
| chr5:81380579
|
A | G | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0002c0002t0007g0211 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197+5178T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380579 | ||||||
| chr5:81380580
|
AG | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0057others(58): Show | 65 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.197+5176delC | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380580 | ||||||
| chr5:81380581
|
G | A | 177 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0042others(174): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.197+5176C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380581 | ||||||
| chr5:81380587
|
A | G | 2 | a0001c0001t0003g0194a0001c0001t0003g0237 | 2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.197+5170T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380587 | ||||||
| chr5:81380610
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.197+5147C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380610 | ||||||
| chr5:81380721
|
A | T | 92 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(89): Show | 98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+5036T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380721 | ||||||
| chr5:81380726
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.197+5031A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380726 | ||||||
| chr5:81380732
|
G | A | 2 | a0001c0001t0002g0002a0002c0002t0002g0231 | 4 | HG01099.hp2 NA18972.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+5025C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380732 | ||||||
| chr5:81380741
|
A | G | 1 | a0001c0001t0005g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197+5016T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380741 | ||||||
| chr5:81381003
|
A | C | 1 | a0002c0002t0002g0064 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.197+4754T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381003 | ||||||
| chr5:81381067
|
C | T | 157 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(154): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.197+4690G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381067 | ||||||
| chr5:81381068
|
C | T | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+4689G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381068 | ||||||
| chr5:81381201
|
G | A | 1 | a0001c0001t0003g0176 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.197+4556C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381201 | ||||||
| chr5:81381442
|
G | A | 1 | a0001c0001t0004g0177 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.197+4315C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381442 | ||||||
| chr5:81381487
|
T | C | 92 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(89): Show | 98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+4270A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381487 | ||||||
| chr5:81381494
|
T | C | 92 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(89): Show | 98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+4263A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381494 | ||||||
| chr5:81381533
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.197+4224C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381533 | ||||||
| chr5:81381989
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.197+3768C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381989 | ||||||
| chr5:81382103
|
ACT | A | 3 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0005g0158 | 3 | HG02572.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.197+3652_197+3653d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382103 | ||||||
| chr5:81382283
|
C | G | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+3474G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382283 | ||||||
| chr5:81382477
|
G | T | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+3280C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382477 | ||||||
| chr5:81382512
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(35): Show | 41 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.197+3245T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382512 | ||||||
| chr5:81382579
|
C | T | 23 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(20): Show | 25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.197+3178G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382579 | ||||||
| chr5:81382604
|
C | A | 6 | a0001c0001t0001g0195a0001c0001t0003g0149a0001c0001t0004g0015others(3): Show | 6 | HG02451.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+3153G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382604 | ||||||
| chr5:81382617
|
T | C | 3 | a0001c0001t0003g0194a0001c0001t0003g0237a0002c0002t0007g0211 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197+3140A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382617 | ||||||
| chr5:81382632
|
A | G | 38 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(35): Show | 41 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.197+3125T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382632 | ||||||
| chr5:81382694
|
C | T | 7 | a0001c0001t0003g0020a0001c0001t0004g0004a0001c0001t0004g0016others(4): Show | 8 | HG01109.hp2 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+3063G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382694 | ||||||
| chr5:81382831
|
G | T | 38 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(35): Show | 41 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.197+2926C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382831 | ||||||
| chr5:81383045
|
A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0123 | 2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.197+2712T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383045 | ||||||
| chr5:81383159
|
C | T | 2 | a0003c0003t0004g0011a0003c0003t0004g0198 | 3 | HG01243.hp1 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.197+2598G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383159 | ||||||
| chr5:81383188
|
G | T | 1 | a0001c0007t0004g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197+2569C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383188 | ||||||
| chr5:81383331
|
C | A | 102 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(99): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.197+2426G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383331 | ||||||
| chr5:81383381
|
A | C | 1 | a0002c0002t0002g0064 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.197+2376T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383381 | ||||||
| chr5:81383382
|
A | C | 1 | a0001c0001t0001g0260 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.197+2375T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383382 | ||||||
| chr5:81383395
|
A | G | 8 | a0001c0001t0001g0039a0001c0001t0001g0139a0001c0001t0002g0077others(5): Show | 8 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+2362T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383395 | ||||||
| chr5:81383526
|
A | G | 116 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(113): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.197+2231T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383526 | ||||||
| chr5:81383530
|
T | C | 116 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(113): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.197+2227A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383530 | ||||||
| chr5:81383671
|
C | G | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.197+2086G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383671 | ||||||
| chr5:81383808
|
TTTTTAAA others(3): Show |
T | 1 | a0001c0001t0001g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.197+1939_197+1948d others(12): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383808 | ||||||
| chr5:81383819
|
C | G | 1 | a0001c0001t0001g0221 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.197+1938G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383819 | ||||||
| chr5:81383886
|
T | G | 23 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(20): Show | 25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.197+1871A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383886 | ||||||
| chr5:81383974
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.197+1783C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383974 | ||||||
| chr5:81384107
|
C | T | 9 | a0001c0001t0001g0195a0001c0001t0002g0146a0001c0001t0002g0210others(6): Show | 9 | HG02451.hp1 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+1650G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384107 | ||||||
| chr5:81384117
|
C | CT | 70 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0057others(67): Show | 74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.197+1639dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384117 | ||||||
| chr5:81384117
|
C | CTT | 21 | a0001c0001t0001g0166a0001c0001t0003g0152a0001c0001t0003g0168others(18): Show | 21 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.197+1638_197+1639d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384117 | ||||||
| chr5:81384270
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+1487C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384270 | ||||||
| chr5:81384273
|
C | T | 12 | a0001c0001t0003g0003a0001c0001t0003g0239a0001c0001t0003g0240others(9): Show | 14 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.197+1484G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384273 | ||||||
| chr5:81384329
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.197+1428G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384329 | ||||||
| chr5:81384330
|
G | A | 19 | a0001c0001t0001g0166a0001c0001t0003g0165a0001c0001t0003g0168others(16): Show | 19 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.197+1427C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384330 | ||||||
| chr5:81384430
|
G | A | 22 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.197+1327C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384430 | ||||||
| chr5:81384610
|
T | G | 11 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0212others(8): Show | 12 | HG02559.hp2 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.197+1147A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384610 | ||||||
| chr5:81384682
|
G | A | 30 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0121others(27): Show | 32 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.197+1075C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384682 | ||||||
| chr5:81384741
|
T | G | 21 | a0001c0001t0001g0166a0001c0001t0003g0152a0001c0001t0003g0165others(18): Show | 21 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.197+1016A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384741 | ||||||
| chr5:81384840
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.197+917C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384840 | ||||||
| chr5:81384906
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.197+851C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384906 | ||||||
| chr5:81385001
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.197+756A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385001 | ||||||
| chr5:81385006
|
A | G | 3 | a0001c0001t0003g0159a0001c0001t0003g0234a0001c0001t0004g0160 | 3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.197+751T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385006 | ||||||
| chr5:81385072
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.197+685G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385072 | ||||||
| chr5:81385247
|
G | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(84): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+510C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385247 | ||||||
| chr5:81385480
|
G | A | 1 | a0001c0001t0004g0249 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.197+277C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385480 | ||||||
| chr5:81385483
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.197+274T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385483 | ||||||
| chr5:81385485
|
T | C | 1 | a0001c0001t0003g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197+272A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385485 | ||||||
| chr5:81385731
|
A | G | 3 | a0001c0001t0003g0159a0001c0001t0003g0234a0001c0001t0004g0160 | 3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.197+26T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385731 | ||||||
| chr5:81386372
|
T | C | 3 | a0001c0001t0003g0159a0001c0001t0003g0234a0001c0001t0004g0160 | 3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.128-546A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386372 | ||||||
| chr5:81386482
|
T | G | 1 | a0001c0001t0003g0179 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.128-656A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386482 | ||||||
| chr5:81386499
|
G | A | 3 | a0001c0001t0003g0159a0001c0001t0003g0234a0001c0001t0004g0160 | 3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.128-673C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386499 | ||||||
| chr5:81386502
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.128-676A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386502 | ||||||
| chr5:81386896
|
C | T | 65 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0002g0059others(62): Show | 69 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.128-1070G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386896 | ||||||
| chr5:81386947
|
A | G | 2 | a0001c0001t0003g0014a0001c0001t0003g0203 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.128-1121T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386947 | ||||||
| chr5:81386991
|
T | C | 2 | a0001c0001t0002g0210a0001c0001t0003g0145 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.128-1165A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386991 | ||||||
| chr5:81386994
|
C | CT | 23 | a0001c0001t0001g0057a0001c0001t0001g0195a0001c0001t0001g0196others(20): Show | 24 | HG00609.hp1 HG01070.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.128-1169_128-1168i others(3): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | ||||||
| chr5:81386994
|
CA | C | 45 | a0001c0001t0002g0146a0001c0001t0002g0214a0001c0001t0003g0014others(42): Show | 47 | HG00099.hp1 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.128-1169delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | ||||||
| chr5:81386994
|
CAT | C | 18 | a0001c0001t0001g0166a0001c0001t0003g0152a0001c0001t0003g0168others(15): Show | 18 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.128-1170_128-1169d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | ||||||
| chr5:81386994
|
CATTTTTT others(4): Show |
C | 3 | a0001c0001t0003g0159a0001c0001t0003g0234a0001c0001t0004g0160 | 3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.128-1179_128-1169d others(13): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | ||||||
| chr5:81386994
|
CATTTTTT others(8): Show |
C | 23 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(20): Show | 24 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.128-1183_128-1169d others(17): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | ||||||
| chr5:81386995
|
A | AT | 12 | a0001c0001t0001g0047a0001c0001t0001g0063a0001c0001t0001g0066others(9): Show | 12 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-1170dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386995 | ||||||
| chr5:81386995
|
A | T | 63 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0065others(60): Show | 69 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.128-1169T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386995 | ||||||
| chr5:81386995
|
AT | A | 12 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0127others(9): Show | 12 | HG00140.hp1 HG00597.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-1170delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386995 | ||||||
| chr5:81387019
|
C | T | 26 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(23): Show | 27 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.128-1193G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387019 | ||||||
| chr5:81387048
|
C | T | 75 | a0001c0001t0001g0166a0001c0001t0001g0195a0001c0001t0001g0196others(72): Show | 78 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.128-1222G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387048 | ||||||
| chr5:81387532
|
C | CT | 46 | a0001c0001t0001g0012a0001c0001t0001g0057a0001c0001t0001g0063others(43): Show | 51 | HG00323.hp1 HG01106.hp2 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.128-1707dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387532 | ||||||
| chr5:81387532
|
CT | C | 33 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0136others(30): Show | 33 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.128-1707delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387532 | ||||||
| chr5:81387604
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.128-1778G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387604 | ||||||
| chr5:81387615
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 6 | HG02559.hp2 HG03139.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-1789C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387615 | ||||||
| chr5:81387675
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.128-1849T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387675 | ||||||
| chr5:81387927
|
G | T | 4 | a0001c0001t0001g0053a0001c0001t0002g0052a0001c0001t0002g0054others(1): Show | 4 | HG00609.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-2101C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387927 | ||||||
| chr5:81388055
|
C | T | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128-2229G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388055 | ||||||
| chr5:81388094
|
T | C | 1 | a0001c0007t0004g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.128-2268A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388094 | ||||||
| chr5:81388447
|
G | A | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.128-2621C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388447 | ||||||
| chr5:81388483
|
G | A | 23 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(20): Show | 24 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.128-2657C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388483 | ||||||
| chr5:81388509
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-2683C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388509 | ||||||
| chr5:81388624
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0002g0050 | 2 | HG00597.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.128-2798G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388624 | ||||||
| chr5:81388776
|
T | C | 2 | a0001c0001t0003g0250a0001c0001t0004g0251 | 2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.128-2950A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388776 | ||||||
| chr5:81388803
|
T | C | 3 | a0002c0002t0001g0154a0002c0002t0001g0180a0005c0006t0002g0155 | 3 | HG01884.hp1 HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.128-2977A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388803 | ||||||
| chr5:81388811
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.128-2985A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388811 | ||||||
| chr5:81388860
|
C | T | 2 | a0001c0001t0002g0048a0001c0001t0003g0045 | 2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.128-3034G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388860 | ||||||
| chr5:81388881
|
G | C | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG01168.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.128-3055C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388881 | ||||||
| chr5:81388909
|
T | G | 2 | a0001c0001t0003g0147a0001c0001t0003g0235 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.128-3083A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388909 | ||||||
| chr5:81388996
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.128-3170G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388996 | ||||||
| chr5:81388997
|
G | A | 106 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0166others(103): Show | 111 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.128-3171C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388997 | ||||||
| chr5:81389163
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.128-3337G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389163 | ||||||
| chr5:81389280
|
G | A | 102 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0166others(99): Show | 107 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.128-3454C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389280 | ||||||
| chr5:81389665
|
T | C | 36 | a0001c0001t0003g0014a0001c0001t0003g0017a0001c0001t0003g0018others(33): Show | 38 | HG00099.hp1 HG01109.hp2 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.128-3839A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389665 | ||||||
| chr5:81389758
|
C | G | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.128-3932G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389758 | ||||||
| chr5:81389770
|
GCCTGCCT others(968): Show |
G | 5 | a0001c0001t0003g0199a0001c0001t0003g0200a0002c0002t0003g0201others(2): Show | 6 | HG00323.hp1 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+3243_128-3945d others(2): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389770 | ||||||
| chr5:81389792
|
A | G | 34 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.128-3966T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389792 | ||||||
| chr5:81389941
|
T | C | 3 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0004g0236 | 3 | HG01891.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.127+4047A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389941 | ||||||
| chr5:81389955
|
A | AT | 17 | a0001c0001t0001g0047a0001c0001t0001g0217a0001c0001t0002g0046others(14): Show | 17 | HG00423.hp1 HG00438.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+4032dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389955 | ||||||
| chr5:81389955
|
A | T | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+4033T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389955 | ||||||
| chr5:81389955
|
AT | A | 19 | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0002g0137others(16): Show | 20 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.127+4032delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389955 | ||||||
| chr5:81390040
|
G | A | 11 | a0001c0001t0003g0010a0001c0001t0003g0184a0001c0001t0003g0186others(8): Show | 12 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+3948C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390040 | ||||||
| chr5:81390076
|
T | A | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.127+3912A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390076 | ||||||
| chr5:81390172
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.127+3816C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390172 | ||||||
| chr5:81390199
|
C | T | 23 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(20): Show | 24 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.127+3789G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390199 | ||||||
| chr5:81390481
|
C | A | 21 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(18): Show | 22 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.127+3507G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390481 | ||||||
| chr5:81390485
|
C | T | 1 | a0001c0001t0003g0239 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127+3503G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390485 | ||||||
| chr5:81390662
|
C | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0002g0197 | 3 | HG02717.hp2 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.127+3326G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390662 | ||||||
| chr5:81390767
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02015.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.127+3221C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390767 | ||||||
| chr5:81390891
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.127+3097A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390891 | ||||||
| chr5:81391121
|
A | C | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+2867T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391121 | ||||||
| chr5:81391314
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+2674C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391314 | ||||||
| chr5:81391406
|
A | C | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+2582T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391406 | ||||||
| chr5:81391426
|
G | A | 1 | a0002c0002t0003g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127+2562C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391426 | ||||||
| chr5:81391438
|
G | A | 5 | a0001c0001t0003g0199a0001c0001t0003g0200a0002c0002t0003g0201others(2): Show | 6 | HG00323.hp1 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+2550C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391438 | ||||||
| chr5:81391473
|
C | T | 3 | a0001c0001t0002g0013a0001c0001t0002g0215a0001c0001t0002g0216 | 4 | HG01258.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+2515G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391473 | ||||||
| chr5:81391576
|
G | C | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127+2412C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391576 | ||||||
| chr5:81391588
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.127+2400C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391588 | ||||||
| chr5:81391685
|
C | T | 149 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0166others(146): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.127+2303G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391685 | ||||||
| chr5:81391754
|
G | T | 43 | a0001c0001t0001g0166a0001c0001t0003g0010a0001c0001t0003g0152others(40): Show | 44 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.127+2234C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391754 | ||||||
| chr5:81391776
|
G | A | 1 | a0001c0005t0003g0202 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+2212C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391776 | ||||||
| chr5:81391866
|
G | C | 22 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+2122C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391866 | ||||||
| chr5:81391870
|
A | G | 22 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+2118T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391870 | ||||||
| chr5:81391972
|
G | A | 76 | a0001c0001t0001g0166a0001c0001t0001g0195a0001c0001t0001g0196others(73): Show | 80 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.127+2016C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391972 | ||||||
| chr5:81392030
|
T | C | 1 | a0001c0001t0003g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+1958A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392030 | ||||||
| chr5:81392054
|
G | A | 1 | a0002c0002t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127+1934C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392054 | ||||||
| chr5:81392136
|
T | G | 1 | a0002c0002t0007g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127+1852A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392136 | ||||||
| chr5:81392356
|
G | A | 1 | a0001c0001t0002g0142 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.127+1632C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392356 | ||||||
| chr5:81392539
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.127+1449C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392539 | ||||||
| chr5:81392750
|
TA | T | 68 | a0001c0001t0001g0012a0001c0001t0001g0039a0001c0001t0001g0166others(65): Show | 72 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.127+1237delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392750 | ||||||
| chr5:81392750
|
TAA | T | 29 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(26): Show | 30 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.127+1236_127+1237d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392750 | ||||||
| chr5:81392902
|
A | C | 1 | a0001c0001t0003g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+1086T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392902 | ||||||
| chr5:81392998
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.127+990G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392998 | ||||||
| chr5:81393136
|
G | C | 2 | a0001c0001t0002g0204a0001c0001t0002g0205 | 2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+852C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393136 | ||||||
| chr5:81393174
|
A | G | 1 | a0001c0001t0005g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127+814T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393174 | ||||||
| chr5:81393189
|
T | A | 148 | a0001c0001t0001g0012a0001c0001t0001g0166a0001c0001t0001g0195others(145): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.127+799A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393189 | ||||||
| chr5:81393261
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127+727C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393261 | ||||||
| chr5:81393279
|
T | C | 1 | a0002c0002t0002g0207 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127+709A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393279 | ||||||
| chr5:81393383
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.127+605A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393383 | ||||||
| chr5:81393623
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+365C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393623 | ||||||
| chr5:81393632
|
G | A | 22 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+356C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393632 | ||||||
| chr5:81393653
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127+335C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393653 | ||||||
| chr5:81393702
|
T | TCAA | 5 | a0001c0001t0001g0012a0001c0001t0001g0212a0001c0001t0001g0213others(2): Show | 6 | HG02258.hp1 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+283_127+285dup others(3): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393702 | ||||||
| chr5:81393715
|
C | CA | 22 | a0001c0001t0001g0217a0001c0001t0001g0219a0001c0001t0001g0221others(19): Show | 23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+272dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393715 | ||||||
| chr5:81393715
|
C | CAACA | 25 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(22): Show | 27 | HG00099.hp1 HG01109.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.127+269_127+272dup others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393715 | ||||||
| chr5:81393911
|
A | AC | 26 | a0001c0001t0003g0014a0001c0001t0003g0017a0001c0001t0003g0018others(23): Show | 28 | HG00099.hp1 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+76dupG | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393911 | ||||||
| chr5:81393911
|
AC | A | 27 | a0001c0001t0003g0003a0001c0001t0003g0234a0001c0001t0003g0235others(24): Show | 29 | HG01106.hp2 HG01123.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.127+76delG | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393911 | ||||||
| chr5:81393917
|
C | A | 2 | a0001c0001t0001g0260a0001c0001t0002g0261 | 2 | HG00140.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.127+71G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393917 |