Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8846 |
|---|---|
| ensemblid | ENSG00000100601.10 |
| hgncid | 17911 |
| symbol | ALKBH1 |
| name | alkB homolog 1, histone H2A dioxygenase |
| refseq_nuc | NM_006020.3 |
| refseq_prot | NP_006011.2 |
| ensembl_nuc | ENST00000216489.8 |
| ensembl_prot | ENSP00000216489.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 77672404 |
| end | 77708023 |
| strand | - |
| ver | v1.2 |
| region | chr14:77672404-77708023 |
| region5000 | chr14:77667404-77713023 |
| regionname0 | ALKBH1_chr14_77672404_77708023 |
| regionname5000 | ALKBH1_chr14_77667404_77713023 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 389 | 313 | 86 | 46 | 142 | 12 | 25 | 107 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002 | 0/0 | 389 | 38 | 4 | 10 | 17 | 3 | 4 | 16 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0003 | 0/0 | 389 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0004 | 0/0 | 389 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0005 | 0/0 | 389 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0006 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0007 | 0/0 | 389 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0008 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0009 | 0/0 | 389 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1170 | 312 | 86 | 46 | 141 | 12 | 25 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0002 | 0/0 | 1170 | 24 | 2 | 10 | 7 | 2 | 3 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0003 | 0/0 | 1170 | 12 | 0 | 0 | 10 | 1 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0004 | 0/0 | 1170 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0005 | 0/0 | 1170 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0006 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0007 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0008 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0009 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0010 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0011 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| c0012 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1428 | 119 | 9 | 26 | 64 | 5 | 15 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0002 | 1/1 | 1428 | 96 | 53 | 5 | 26 | 2 | 8 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0003 | 0/0 | 1428 | 72 | 9 | 11 | 47 | 1 | 4 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0004 | 0/0 | 1428 | 27 | 5 | 10 | 7 | 2 | 3 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0005 | 0/0 | 1428 | 19 | 12 | 3 | 0 | 4 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0006 | 0/0 | 1428 | 14 | 0 | 2 | 10 | 2 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0007 | 0/0 | 1429 | 5 | 0 | 0 | 5 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0008 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0009 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0010 | 0/0 | 1428 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0011 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0012 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0013 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| t0014 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 14 | 3 | 3 | 6 | 1 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0002 | 0/0 | 13 | 0 | 4 | 5 | 2 | 2 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0004 | 0/0 | 8 | 0 | 1 | 3 | 0 | 4 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0005 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0012 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1170 | 312 | 86 | 46 | 141 | 12 | 25 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0011 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002c0002 | 0/0 | 1170 | 24 | 2 | 10 | 7 | 2 | 3 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002c0003 | 0/0 | 1170 | 12 | 0 | 0 | 10 | 1 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002c0005 | 0/0 | 1170 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0003c0004 | 0/0 | 1170 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0004c0012 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0005c0006 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0006c0007 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0007c0008 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0008c0010 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0009c0009 | 0/0 | 1170 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2597 | 115 | 9 | 26 | 63 | 5 | 12 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0002 | 1/1 | 2597 | 96 | 53 | 5 | 26 | 2 | 8 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0003 | 0/0 | 2597 | 71 | 9 | 11 | 46 | 1 | 4 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0005 | 0/0 | 2597 | 19 | 12 | 3 | 0 | 4 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0007 | 0/0 | 2598 | 5 | 0 | 0 | 5 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0008 | 0/0 | 2597 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0010 | 0/0 | 2597 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0011 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0013 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0001t0014 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0001c0011t0003 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002c0002t0004 | 0/0 | 2597 | 24 | 2 | 10 | 7 | 2 | 3 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002c0003t0006 | 0/0 | 2597 | 11 | 0 | 0 | 10 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002c0003t0009 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0002c0005t0004 | 0/0 | 2597 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0003c0004t0006 | 0/0 | 2597 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0004c0012t0001 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0005c0006t0001 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0006c0007t0012 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0007c0008t0001 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0008c0010t0004 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| a0009c0009t0001 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | copy fasta | chr14 | 77667404 | 77713023 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 13 | 0 | 4 | 5 | 2 | 2 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 1 | 3 | 0 | 4 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0001 | 0/0 | 14 | 3 | 3 | 6 | 1 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0010g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0013g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0014g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0011t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0009g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0005t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0005t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0003c0004t0006g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0003c0004t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0003c0004t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0004c0012t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0005c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0006c0007t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0007c0008t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0008c0010t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0009c0009t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0016 | EUR | GBR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0016 | EUR | FIN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | FIN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00323 | hp1 | a0002 | c0002 | t0004 | g0074 | EUR | FIN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00323 | hp2 | a0002 | c0002 | t0004 | g0080 | EUR | FIN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00408 | hp2 | a0001 | c0001 | t0014 | g0038 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00738 | hp2 | a0002 | c0002 | t0004 | g0077 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00741 | hp2 | a0002 | c0002 | t0004 | g0083 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0271 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0070 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01167 | hp1 | a0002 | c0002 | t0004 | g0075 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01167 | hp2 | a0002 | c0002 | t0004 | g0085 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01168 | hp2 | a0002 | c0002 | t0004 | g0076 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01257 | hp2 | a0003 | c0004 | t0006 | g0066 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01258 | hp2 | a0003 | c0004 | t0006 | g0067 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0259 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01496 | hp1 | a0002 | c0002 | t0004 | g0091 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01496 | hp2 | a0002 | c0002 | t0004 | g0079 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0030 | EUR | IBS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0030 | EUR | IBS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0090 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0078 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0214 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | CDX | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CDX | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02165 | hp1 | a0002 | c0002 | t0004 | g0071 | EAS | CDX | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02293 | hp2 | a0002 | c0002 | t0004 | g0087 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02602 | hp2 | a0002 | c0002 | t0004 | g0089 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02630 | hp1 | a0002 | c0002 | t0004 | g0084 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02735 | hp2 | a0001 | c0001 | t0013 | g0225 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02738 | hp1 | a0007 | c0008 | t0001 | g0206 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0263 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0268 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03195 | hp2 | a0008 | c0010 | t0004 | g0273 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0260 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03486 | hp1 | a0002 | c0005 | t0004 | g0088 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0262 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03688 | hp2 | a0002 | c0002 | t0004 | g0081 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03710 | hp2 | a0002 | c0003 | t0009 | g0130 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | BEB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04228 | hp1 | a0009 | c0009 | t0001 | g0217 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04228 | hp2 | a0002 | c0002 | t0004 | g0086 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0043 | AFR | YRI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0025 | EAS | CHB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | CHB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | YRI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18943 | hp1 | a0002 | c0003 | t0006 | g0021 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18946 | hp1 | a0002 | c0003 | t0006 | g0126 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18947 | hp1 | a0002 | c0003 | t0006 | g0131 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18951 | hp1 | a0002 | c0003 | t0006 | g0127 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18953 | hp1 | a0002 | c0003 | t0006 | g0010 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18960 | hp1 | a0002 | c0003 | t0006 | g0010 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18961 | hp2 | a0002 | c0002 | t0004 | g0069 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18966 | hp1 | a0002 | c0003 | t0006 | g0010 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18966 | hp2 | a0004 | c0012 | t0001 | g0215 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18994 | hp1 | a0002 | c0003 | t0006 | g0128 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18994 | hp2 | a0002 | c0002 | t0004 | g0072 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18995 | hp2 | a0002 | c0002 | t0004 | g0073 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19007 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19010 | hp2 | a0001 | c0011 | t0003 | g0098 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0266 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0167 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19058 | hp2 | a0001 | c0001 | t0007 | g0189 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19065 | hp1 | a0002 | c0003 | t0006 | g0021 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19081 | hp1 | a0002 | c0003 | t0006 | g0051 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | YRI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ASW | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ASW | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20752 | hp2 | a0002 | c0003 | t0006 | g0129 | EUR | TSI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20805 | hp1 | a0003 | c0004 | t0006 | g0068 | EUR | TSI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20905 | hp1 | a0005 | c0006 | t0001 | g0059 | SAS | GIH | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | GIH | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02486 | hp1 | a0006 | c0007 | t0012 | g0057 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | USA | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | USA | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | USA | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | USA | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA21309 | hp1 | a0002 | c0005 | t0004 | g0082 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0138 | REF | REF | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0233 | REF | REF | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77673847
|
C | T | 1 | a0009 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1135G>A | p.Glu379Lys | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1154/2597 | 1135/1170 | 379/389 | chr14 | 77673847 | ||
| chr14:77673913
|
G | A | 1 | a0008 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1069C>T | p.Pro357Ser | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1088/2597 | 1069/1170 | 357/389 | chr14 | 77673913 | ||
| chr14:77674012
|
T | A | 3 | a0002a0003a0008 | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
missense_variant | MODERATE | c.970A>T | p.Met324Leu | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 989/2597 | 970/1170 | 324/389 | chr14 | 77674012 | ||
| chr14:77675702
|
C | T | 1 | a0007 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.694G>A | p.Val232Ile | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/6 | 713/2597 | 694/1170 | 232/389 | chr14 | 77675702 | ||
| chr14:77679909
|
C | T | 1 | a0006 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.517G>A | p.Val173Ile | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/6 | 536/2597 | 517/1170 | 173/389 | chr14 | 77679909 | ||
| chr14:77679950
|
C | T | 1 | a0005 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.476G>A | p.Arg159Gln | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/6 | 495/2597 | 476/1170 | 159/389 | chr14 | 77679950 | ||
| chr14:77694788
|
C | T | 1 | a0003 | 3 | HG01257.hp2 HG01258.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.405G>A | p.Met135Ile | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/6 | 424/2597 | 405/1170 | 135/389 | chr14 | 77694788 | ||
| chr14:77704449
|
G | C | 1 | a0004 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.212C>G | p.Ser71Cys | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/6 | 231/2597 | 212/1170 | 71/389 | chr14 | 77704449 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77673986
|
G | A | 3 | a0002c0002a0002c0005a0008c0010 | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
synonymous_variant | LOW | c.996C>T | p.Ser332Ser | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1015/2597 | 996/1170 | 332/389 | chr14 | 77673986 | ||
| chr14:77674220
|
A | G | 1 | a0002c0005 | 2 | HG03486.hp1 NA21309.hp1 |
synonymous_variant | LOW | c.762T>C | p.Phe254Phe | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 781/2597 | 762/1170 | 254/389 | chr14 | 77674220 | ||
| chr14:77675811
|
G | A | 1 | a0001c0011 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.585C>T | p.Asp195Asp | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/6 | 604/2597 | 585/1170 | 195/389 | chr14 | 77675811 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77672426
|
T | C | 1 | a0002c0003t0009 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1386A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1386 | chr14 | 77672426 | |||||
| chr14:77672431
|
A | G | 1 | a0006c0007t0012 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1381T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1381 | chr14 | 77672431 | |||||
| chr14:77672682
|
C | T | 8 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(5): Show | 127 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1130G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1130 | chr14 | 77672682 | |||||
| chr14:77672693
|
T | C | 1 | a0001c0001t0008 | 2 | HG02647.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1119A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1119 | chr14 | 77672693 | |||||
| chr14:77672698
|
G | A | 1 | a0001c0001t0013 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 1114 | chr14 | 77672698 | |||||
| chr14:77672815
|
G | T | 1 | a0001c0001t0005 | 19 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*997C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 997 | chr14 | 77672815 | |||||
| chr14:77672949
|
T | C | 6 | a0002c0002t0004a0002c0003t0006a0002c0003t0009others(3): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*863A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 863 | chr14 | 77672949 | |||||
| chr14:77672991
|
G | GA | 1 | a0001c0001t0007 | 5 | HG00408.hp1 NA18747.hp1 NA18940.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*820dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 820 | chr14 | 77672991 | |||||
| chr14:77673232
|
A | T | 1 | a0001c0001t0011 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 580 | chr14 | 77673232 | |||||
| chr14:77673262
|
C | T | 1 | a0001c0001t0010 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*550G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 550 | chr14 | 77673262 | |||||
| chr14:77673645
|
C | A | 3 | a0001c0001t0003a0001c0001t0014a0001c0011t0003 | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*167G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 167 | chr14 | 77673645 | |||||
| chr14:77673659
|
G | A | 1 | a0001c0001t0014 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*153C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 153 | chr14 | 77673659 | |||||
| chr14:77673677
|
C | T | 3 | a0002c0003t0006a0002c0003t0009a0003c0004t0006 | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 6/6 | 135 | chr14 | 77673677 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77674412
|
G | A | 1 | a0002c0002t0004g0087 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.741-171C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674412 | ||||||
| chr14:77674446
|
T | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.741-205A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674446 | ||||||
| chr14:77674550
|
GT | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 140 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.741-310delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674550 | ||||||
| chr14:77674686
|
G | C | 8 | a0002c0002t0004g0080a0002c0002t0004g0081a0002c0002t0004g0084others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.741-445C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674686 | ||||||
| chr14:77674697
|
C | T | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.741-456G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674697 | ||||||
| chr14:77674909
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.741-668G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674909 | ||||||
| chr14:77674947
|
A | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.741-706T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674947 | ||||||
| chr14:77674952
|
C | A | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.740+704G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674952 | ||||||
| chr14:77674954
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.740+702G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674954 | ||||||
| chr14:77674960
|
G | A | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(231): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.740+696C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77674960 | ||||||
| chr14:77675014
|
T | C | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.740+642A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675014 | ||||||
| chr14:77675049
|
T | C | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.740+607A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675049 | ||||||
| chr14:77675151
|
G | C | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.740+505C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675151 | ||||||
| chr14:77675250
|
C | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.740+406G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675250 | ||||||
| chr14:77675271
|
A | G | 15 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0258others(12): Show | 18 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.740+385T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675271 | ||||||
| chr14:77675271
|
A | T | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.740+385T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675271 | ||||||
| chr14:77675309
|
C | T | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.740+347G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675309 | ||||||
| chr14:77675361
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.740+295C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675361 | ||||||
| chr14:77675400
|
T | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.740+256A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675400 | ||||||
| chr14:77675433
|
C | CA | 64 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(61): Show | 71 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.740+222dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675433 | ||||||
| chr14:77675515
|
A | G | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.740+141T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675515 | ||||||
| chr14:77675998
|
C | CT | 28 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(25): Show | 30 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.547-150dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77675998 | ||||||
| chr14:77675998
|
C | CTT | 14 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(11): Show | 16 | HG01496.hp1 HG01884.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.547-151_547-150dup others(2): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77675998 | ||||||
| chr14:77675998
|
CT | C | 21 | a0001c0001t0001g0192a0001c0001t0001g0195a0001c0001t0001g0202others(18): Show | 21 | HG01168.hp2 HG02145.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.547-150delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77675998 | ||||||
| chr14:77676064
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.547-215T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676064 | ||||||
| chr14:77676112
|
T | G | 2 | a0001c0001t0005g0260a0001c0001t0005g0261 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.547-263A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676112 | ||||||
| chr14:77676162
|
AT | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(176): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.547-314delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676162 | ||||||
| chr14:77676278
|
C | G | 25 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(22): Show | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.547-429G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676278 | ||||||
| chr14:77676350
|
T | C | 1 | a0002c0002t0004g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.547-501A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676350 | ||||||
| chr14:77676428
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-579G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676428 | ||||||
| chr14:77676546
|
G | A | 2 | a0001c0001t0002g0135a0001c0001t0002g0140 | 2 | HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.547-697C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676546 | ||||||
| chr14:77676621
|
A | G | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.547-772T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676621 | ||||||
| chr14:77676726
|
T | C | 1 | a0001c0001t0002g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.547-877A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676726 | ||||||
| chr14:77677043
|
C | T | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.547-1194G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677043 | ||||||
| chr14:77677045
|
C | CT | 16 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(13): Show | 18 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.547-1197dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677045 | ||||||
| chr14:77677051
|
T | C | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.547-1202A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677051 | ||||||
| chr14:77677064
|
G | C | 25 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(22): Show | 27 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.547-1215C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677064 | ||||||
| chr14:77677121
|
C | G | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-1272G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677121 | ||||||
| chr14:77677453
|
T | C | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.547-1604A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677453 | ||||||
| chr14:77677570
|
G | A | 38 | a0001c0001t0002g0227a0002c0002t0004g0008a0002c0002t0004g0069others(35): Show | 43 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.547-1721C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677570 | ||||||
| chr14:77677638
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.547-1789G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677638 | ||||||
| chr14:77677742
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.547-1893A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677742 | ||||||
| chr14:77677750
|
G | A | 1 | a0001c0001t0003g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.547-1901C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677750 | ||||||
| chr14:77677827
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.547-1978G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677827 | ||||||
| chr14:77677905
|
G | A | 1 | a0001c0001t0003g0118 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.546+1975C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77677905 | ||||||
| chr14:77678015
|
A | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.546+1865T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678015 | ||||||
| chr14:77678035
|
T | C | 6 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+1845A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678035 | ||||||
| chr14:77678077
|
A | T | 1 | a0001c0001t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.546+1803T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678077 | ||||||
| chr14:77678087
|
C | CA | 60 | a0001c0001t0002g0007a0001c0001t0002g0044a0001c0001t0002g0045others(57): Show | 82 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.546+1792dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678087 | ||||||
| chr14:77678087
|
C | CAA | 99 | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0208others(96): Show | 121 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.546+1791_546+1792d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678087 | ||||||
| chr14:77678087
|
C | CAAA | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(82): Show | 123 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.546+1790_546+1792d others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678087 | ||||||
| chr14:77678087
|
C | CAAAA | 18 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0157others(15): Show | 22 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.546+1789_546+1792d others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678087 | ||||||
| chr14:77678161
|
ATTGAGAT others(12): Show |
A | 1 | a0001c0001t0001g0169 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.546+1700_546+1718d others(21): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678161 | ||||||
| chr14:77678162
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.546+1718A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678162 | ||||||
| chr14:77678208
|
T | TTATGAGG | 3 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0271 | 6 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+1665_546+1671d others(9): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678208 | ||||||
| chr14:77678232
|
C | T | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.546+1648G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678232 | ||||||
| chr14:77678233
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 128 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.546+1647C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678233 | ||||||
| chr14:77678412
|
G | C | 3 | a0001c0001t0002g0023a0001c0001t0002g0132a0001c0001t0002g0136 | 4 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+1468C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678412 | ||||||
| chr14:77678418
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(85): Show | 127 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.546+1462C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678418 | ||||||
| chr14:77678516
|
C | T | 1 | a0002c0002t0004g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.546+1364G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678516 | ||||||
| chr14:77678545
|
C | CA | 31 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0052others(28): Show | 44 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.546+1334dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678545 | ||||||
| chr14:77678545
|
CAA | C | 53 | a0001c0001t0002g0138a0001c0001t0003g0001a0001c0001t0003g0009others(50): Show | 72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.546+1333_546+1334d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678545 | ||||||
| chr14:77678545
|
CAAA | C | 63 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(60): Show | 70 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.546+1332_546+1334d others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678545 | ||||||
| chr14:77678562
|
C | A | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+1318G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678562 | ||||||
| chr14:77678563
|
A | G | 12 | a0002c0003t0006g0010a0002c0003t0006g0021a0002c0003t0006g0051others(9): Show | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.546+1317T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678563 | ||||||
| chr14:77678611
|
T | A | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.546+1269A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678611 | ||||||
| chr14:77678717
|
G | A | 3 | a0001c0001t0003g0093a0001c0001t0003g0094a0001c0001t0003g0118 | 3 | HG02015.hp2 HG02523.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.546+1163C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678717 | ||||||
| chr14:77678787
|
C | G | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.546+1093G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678787 | ||||||
| chr14:77678830
|
T | C | 1 | a0001c0001t0003g0019 | 2 | HG00733.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.546+1050A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678830 | ||||||
| chr14:77678853
|
A | G | 81 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(78): Show | 102 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.546+1027T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678853 | ||||||
| chr14:77678879
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.546+1001C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678879 | ||||||
| chr14:77678907
|
C | A | 1 | a0001c0001t0008g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.546+973G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678907 | ||||||
| chr14:77679092
|
C | T | 1 | a0001c0001t0002g0250 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.546+788G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679092 | ||||||
| chr14:77679109
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.546+771C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679109 | ||||||
| chr14:77679194
|
C | A | 1 | a0001c0001t0001g0256 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.546+686G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679194 | ||||||
| chr14:77679328
|
A | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.546+552T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679328 | ||||||
| chr14:77679341
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.546+539T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679341 | ||||||
| chr14:77679348
|
T | C | 1 | a0001c0001t0002g0250 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.546+532A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679348 | ||||||
| chr14:77679455
|
G | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.546+425C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679455 | ||||||
| chr14:77679475
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0274 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.546+405C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679475 | ||||||
| chr14:77679491
|
T | TGCGATCT others(3): Show |
1 | a0001c0001t0001g0169 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.546+379_546+388dup others(10): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679491 | ||||||
| chr14:77679541
|
T | C | 134 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(131): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.546+339A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679541 | ||||||
| chr14:77679637
|
C | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0274 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.546+243G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679637 | ||||||
| chr14:77679763
|
G | A | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.546+117C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679763 | ||||||
| chr14:77679800
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.546+80G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77679800 | ||||||
| chr14:77680078
|
G | C | 1 | a0001c0001t0002g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.456-108C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680078 | ||||||
| chr14:77680122
|
C | A | 1 | a0004c0012t0001g0215 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.456-152G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680122 | ||||||
| chr14:77680228
|
T | TC | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 147 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.456-259dupG | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680228 | ||||||
| chr14:77680257
|
C | G | 1 | a0001c0001t0002g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.456-287G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680257 | ||||||
| chr14:77680263
|
C | A | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.456-293G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680263 | ||||||
| chr14:77680535
|
C | T | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.456-565G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680535 | ||||||
| chr14:77680674
|
A | ACTCT | 50 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(47): Show | 68 | HG00408.hp2 HG00423.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.456-708_456-705dup others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680674 | ||||||
| chr14:77680677
|
C | CTCT | 8 | a0002c0002t0004g0070a0002c0002t0004g0074a0002c0002t0004g0075others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-708_456-707ins others(3): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTCTTTTT others(1): Show |
12 | a0002c0002t0004g0071a0002c0002t0004g0080a0002c0002t0004g0081others(9): Show | 12 | HG00323.hp2 HG01496.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.456-708_456-707ins others(8): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTCTTTTT others(2): Show |
17 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043others(14): Show | 22 | HG01167.hp2 HG01257.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.456-708_456-707ins others(9): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTCTTTTT others(3): Show |
1 | a0003c0004t0006g0067 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.456-708_456-707ins others(10): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTCTTTTT others(14): Show |
1 | a0001c0001t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.456-708_456-707ins others(21): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTCTTTTT others(16): Show |
1 | a0001c0001t0002g0048 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.456-708_456-707ins others(23): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTTTTTTT others(1): Show |
9 | a0001c0001t0002g0023a0001c0001t0002g0132a0001c0001t0002g0133others(6): Show | 10 | HG01516.hp1 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.456-715_456-708dup others(8): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0002g0022a0001c0001t0002g0139a0001c0001t0002g0141others(4): Show | 8 | HG00280.hp2 HG01081.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-716_456-708dup others(9): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0134a0001c0001t0002g0142 | 2 | HG01109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.456-717_456-708dup others(10): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680677
|
CT | C | 23 | a0001c0001t0001g0154a0001c0001t0002g0015a0001c0001t0002g0222others(20): Show | 28 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.456-708delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680677 | ||||||
| chr14:77680679
|
T | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 148 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.456-709A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680679 | ||||||
| chr14:77680680
|
T | C | 23 | a0001c0001t0001g0154a0001c0001t0002g0015a0001c0001t0002g0222others(20): Show | 28 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.456-710A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680680 | ||||||
| chr14:77680681
|
T | C | 1 | a0001c0001t0005g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.456-711A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680681 | ||||||
| chr14:77680683
|
T | C | 1 | a0002c0003t0006g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.456-713A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680683 | ||||||
| chr14:77680686
|
T | C | 1 | a0001c0001t0003g0111 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.456-716A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680686 | ||||||
| chr14:77680688
|
T | C | 1 | a0001c0001t0003g0111 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.456-718A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680688 | ||||||
| chr14:77680709
|
C | T | 1 | a0001c0001t0005g0263 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.456-739G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680709 | ||||||
| chr14:77680782
|
C | A | 1 | a0001c0001t0013g0225 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.456-812G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680782 | ||||||
| chr14:77680907
|
C | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0053others(3): Show | 8 | HG00140.hp1 HG01256.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-937G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680907 | ||||||
| chr14:77680958
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 128 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.456-988C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680958 | ||||||
| chr14:77680960
|
GCCA | G | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.456-993_456-991del others(3): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77680960 | ||||||
| chr14:77681067
|
TTC | T | 12 | a0002c0003t0006g0010a0002c0003t0006g0021a0002c0003t0006g0051others(9): Show | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.456-1099_456-1098d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681067 | ||||||
| chr14:77681086
|
T | C | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.456-1116A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681086 | ||||||
| chr14:77681272
|
C | T | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.456-1302G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681272 | ||||||
| chr14:77681320
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.456-1350C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681320 | ||||||
| chr14:77681350
|
C | T | 69 | a0001c0001t0002g0006a0001c0001t0002g0044a0001c0001t0002g0045others(66): Show | 91 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.456-1380G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681350 | ||||||
| chr14:77681436
|
T | C | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.456-1466A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681436 | ||||||
| chr14:77681506
|
G | C | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.456-1536C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681506 | ||||||
| chr14:77681624
|
T | C | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.456-1654A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681624 | ||||||
| chr14:77681828
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.456-1858G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681828 | ||||||
| chr14:77681882
|
C | T | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-1912G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681882 | ||||||
| chr14:77681889
|
C | T | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.456-1919G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77681889 | ||||||
| chr14:77682103
|
T | C | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-2133A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682103 | ||||||
| chr14:77682601
|
G | A | 1 | a0002c0002t0004g0087 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.456-2631C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682601 | ||||||
| chr14:77682699
|
A | G | 16 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0258others(13): Show | 19 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.456-2729T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682699 | ||||||
| chr14:77682729
|
A | G | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-2759T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682729 | ||||||
| chr14:77682769
|
C | G | 16 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0258others(13): Show | 19 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.456-2799G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682769 | ||||||
| chr14:77682854
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.456-2884C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682854 | ||||||
| chr14:77682863
|
A | G | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.456-2893T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682863 | ||||||
| chr14:77682945
|
C | T | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.456-2975G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77682945 | ||||||
| chr14:77683130
|
T | C | 2 | a0001c0001t0003g0032a0001c0001t0003g0040 | 2 | NA18747.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.456-3160A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683130 | ||||||
| chr14:77683143
|
T | C | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-3173A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683143 | ||||||
| chr14:77683149
|
C | CT | 26 | a0001c0001t0001g0026a0001c0001t0001g0151a0001c0001t0001g0163others(23): Show | 30 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.456-3180dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683149 | ||||||
| chr14:77683149
|
C | CTT | 5 | a0001c0001t0002g0244a0001c0001t0005g0266a0001c0001t0005g0271others(2): Show | 6 | HG00408.hp1 HG01070.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.456-3181_456-3180d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683149 | ||||||
| chr14:77683149
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.456-3179G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683149 | ||||||
| chr14:77683149
|
CT | C | 28 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0154others(25): Show | 32 | HG00609.hp1 HG00735.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.456-3180delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683149 | ||||||
| chr14:77683149
|
CTTTT | C | 29 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(26): Show | 31 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.456-3183_456-3180d others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683149 | ||||||
| chr14:77683149
|
CTTTTT | C | 32 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043others(29): Show | 37 | HG00323.hp2 HG01167.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.456-3184_456-3180d others(7): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683149 | ||||||
| chr14:77683149
|
CTTTTTT | C | 56 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(53): Show | 75 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.456-3185_456-3180d others(8): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683149 | ||||||
| chr14:77683168
|
T | G | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.456-3198A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683168 | ||||||
| chr14:77683220
|
G | C | 5 | a0001c0001t0002g0007a0001c0001t0002g0226a0001c0001t0002g0228others(2): Show | 8 | HG00544.hp2 HG00621.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-3250C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683220 | ||||||
| chr14:77683243
|
G | T | 1 | a0001c0001t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456-3273C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683243 | ||||||
| chr14:77683317
|
C | T | 1 | a0001c0001t0007g0159 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.456-3347G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683317 | ||||||
| chr14:77683351
|
C | G | 8 | a0002c0002t0004g0080a0002c0002t0004g0081a0002c0002t0004g0084others(5): Show | 8 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.456-3381G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683351 | ||||||
| chr14:77683375
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.456-3405C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683375 | ||||||
| chr14:77683510
|
A | C | 16 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0258others(13): Show | 19 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.456-3540T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683510 | ||||||
| chr14:77683813
|
C | T | 1 | a0001c0001t0005g0030 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.456-3843G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683813 | ||||||
| chr14:77683884
|
C | T | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-3914G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683884 | ||||||
| chr14:77683993
|
C | T | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.456-4023G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77683993 | ||||||
| chr14:77684052
|
A | G | 2 | a0001c0001t0003g0099a0001c0001t0003g0114 | 2 | NA19067.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.456-4082T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684052 | ||||||
| chr14:77684102
|
G | A | 1 | a0002c0002t0004g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.456-4132C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684102 | ||||||
| chr14:77684324
|
G | T | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-4354C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684324 | ||||||
| chr14:77684368
|
CT | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 140 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.456-4399delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684368 | ||||||
| chr14:77684383
|
C | T | 12 | a0002c0003t0006g0010a0002c0003t0006g0021a0002c0003t0006g0051others(9): Show | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.456-4413G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684383 | ||||||
| chr14:77684530
|
T | G | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.456-4560A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684530 | ||||||
| chr14:77684551
|
A | G | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-4581T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684551 | ||||||
| chr14:77684615
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0168others(4): Show | 9 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.456-4645G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684615 | ||||||
| chr14:77684676
|
T | A | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.456-4706A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684676 | ||||||
| chr14:77684736
|
C | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.456-4766G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684736 | ||||||
| chr14:77684915
|
A | G | 2 | a0001c0001t0005g0258a0001c0001t0005g0265 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.456-4945T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684915 | ||||||
| chr14:77684916
|
A | C | 2 | a0001c0001t0005g0258a0001c0001t0005g0265 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.456-4946T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684916 | ||||||
| chr14:77684983
|
C | T | 16 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0258others(13): Show | 19 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.456-5013G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684983 | ||||||
| chr14:77685017
|
A | G | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.456-5047T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685017 | ||||||
| chr14:77685091
|
G | C | 1 | a0001c0001t0002g0274 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.456-5121C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685091 | ||||||
| chr14:77685197
|
C | T | 8 | a0002c0002t0004g0070a0002c0002t0004g0074a0002c0002t0004g0075others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.456-5227G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685197 | ||||||
| chr14:77685217
|
C | T | 2 | a0001c0001t0005g0258a0001c0001t0005g0265 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.456-5247G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685217 | ||||||
| chr14:77685314
|
G | C | 1 | a0002c0002t0004g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.456-5344C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685314 | ||||||
| chr14:77685436
|
T | TA | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.456-5467dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685436 | ||||||
| chr14:77685450
|
A | C | 27 | a0001c0001t0001g0179a0001c0001t0001g0187a0001c0001t0002g0022others(24): Show | 29 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.456-5480T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685450 | ||||||
| chr14:77685494
|
G | C | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.456-5524C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685494 | ||||||
| chr14:77685558
|
C | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.456-5588G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685558 | ||||||
| chr14:77685623
|
C | CAAAAAAT others(3611): Show |
1 | a0001c0001t0002g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.456-5654_456-5653i others(3620): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685623 | ||||||
| chr14:77685672
|
G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.456-5702C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685672 | ||||||
| chr14:77685672
|
G | C | 1 | a0001c0001t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456-5702C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685672 | ||||||
| chr14:77685705
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0155a0001c0001t0001g0172others(4): Show | 9 | HG00597.hp2 HG00609.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.456-5735A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685705 | ||||||
| chr14:77685767
|
C | T | 14 | a0001c0001t0001g0186a0001c0001t0001g0272a0002c0003t0006g0010others(11): Show | 17 | HG00609.hp1 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.456-5797G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685767 | ||||||
| chr14:77685786
|
T | C | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.456-5816A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685786 | ||||||
| chr14:77685833
|
A | G | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0148others(1): Show | 4 | HG03195.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-5863T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685833 | ||||||
| chr14:77685847
|
C | T | 1 | a0002c0002t0004g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.456-5877G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685847 | ||||||
| chr14:77685943
|
T | C | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.456-5973A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685943 | ||||||
| chr14:77685996
|
A | G | 1 | a0001c0001t0003g0092 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.456-6026T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685996 | ||||||
| chr14:77686013
|
T | G | 4 | a0001c0001t0002g0222a0001c0001t0002g0224a0001c0001t0002g0246others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.456-6043A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686013 | ||||||
| chr14:77686168
|
G | A | 1 | a0001c0001t0003g0111 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.456-6198C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686168 | ||||||
| chr14:77686376
|
C | T | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.456-6406G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686376 | ||||||
| chr14:77686503
|
CAGA | C | 53 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(50): Show | 72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.456-6536_456-6534d others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686503 | ||||||
| chr14:77686578
|
A | C | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.456-6608T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686578 | ||||||
| chr14:77686616
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0183 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.456-6646G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686616 | ||||||
| chr14:77686655
|
C | T | 53 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(50): Show | 72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.456-6685G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686655 | ||||||
| chr14:77686709
|
C | T | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.456-6739G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686709 | ||||||
| chr14:77686714
|
C | G | 3 | a0001c0001t0002g0015a0001c0001t0002g0251a0001c0001t0002g0252 | 5 | HG02922.hp2 HG03471.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.456-6744G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686714 | ||||||
| chr14:77686734
|
C | T | 2 | a0001c0001t0005g0258a0001c0001t0005g0265 | 2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.456-6764G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686734 | ||||||
| chr14:77686783
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.456-6813G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686783 | ||||||
| chr14:77686830
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6860C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686830 | ||||||
| chr14:77686840
|
T | A | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6870A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686840 | ||||||
| chr14:77686843
|
C | A | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6873G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686843 | ||||||
| chr14:77686847
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6877A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686847 | ||||||
| chr14:77686848
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6878A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686848 | ||||||
| chr14:77686850
|
T | G | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6880A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686850 | ||||||
| chr14:77686853
|
A | T | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6883T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686853 | ||||||
| chr14:77686854
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.456-6884G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686854 | ||||||
| chr14:77686926
|
C | T | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.456-6956G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686926 | ||||||
| chr14:77686950
|
CCA | C | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0148others(1): Show | 4 | HG03195.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.456-6982_456-6981d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77686950 | ||||||
| chr14:77687359
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.455+7379G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687359 | ||||||
| chr14:77687498
|
C | CCCTA | 115 | a0001c0001t0002g0022a0001c0001t0002g0044a0001c0001t0002g0045others(112): Show | 140 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.455+7236_455+7239d others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687498 | ||||||
| chr14:77687557
|
ACT | A | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.455+7179_455+7180d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687557 | ||||||
| chr14:77687637
|
T | C | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.455+7101A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687637 | ||||||
| chr14:77687640
|
T | A | 1 | a0001c0001t0003g0119 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.455+7098A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687640 | ||||||
| chr14:77687680
|
C | A | 1 | a0001c0001t0002g0143 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.455+7058G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687680 | ||||||
| chr14:77687703
|
CCT | C | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.455+7033_455+7034d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687703 | ||||||
| chr14:77687726
|
T | C | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+7012A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687726 | ||||||
| chr14:77687790
|
G | T | 58 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(55): Show | 65 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.455+6948C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687790 | ||||||
| chr14:77687825
|
T | TGAGAAAG others(17): Show |
7 | a0001c0001t0002g0015a0001c0001t0002g0222a0001c0001t0002g0224others(4): Show | 9 | HG02055.hp2 HG02647.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.455+6889_455+6912d others(26): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687825 | ||||||
| chr14:77687916
|
C | CTCTT | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.455+6821_455+6822i others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687916 | ||||||
| chr14:77688022
|
C | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0274 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.455+6716G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688022 | ||||||
| chr14:77688084
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.455+6654A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688084 | ||||||
| chr14:77688243
|
AT | A | 114 | a0001c0001t0001g0209a0001c0001t0002g0046a0001c0001t0002g0047others(111): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.455+6494delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688243 | ||||||
| chr14:77688243
|
ATT | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(100): Show | 146 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.455+6493_455+6494d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688243 | ||||||
| chr14:77688402
|
C | T | 17 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(14): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+6336G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688402 | ||||||
| chr14:77688513
|
C | T | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+6225G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688513 | ||||||
| chr14:77688542
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.455+6196G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688542 | ||||||
| chr14:77688553
|
C | CT | 47 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0162others(44): Show | 52 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.455+6184dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688553 | ||||||
| chr14:77688553
|
CTTT | C | 52 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(49): Show | 71 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.455+6182_455+6184d others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688553 | ||||||
| chr14:77688553
|
CTTTT | C | 43 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(40): Show | 48 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.455+6181_455+6184d others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688553 | ||||||
| chr14:77688645
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.455+6093G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688645 | ||||||
| chr14:77688646
|
G | A | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.455+6092C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688646 | ||||||
| chr14:77688666
|
C | T | 1 | a0009c0009t0001g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.455+6072G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688666 | ||||||
| chr14:77688770
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.455+5968G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688770 | ||||||
| chr14:77688786
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(86): Show | 128 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.455+5952C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688786 | ||||||
| chr14:77688861
|
C | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0134a0001c0001t0002g0137others(5): Show | 9 | HG01081.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.455+5877G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688861 | ||||||
| chr14:77688862
|
G | A | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.455+5876C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688862 | ||||||
| chr14:77688935
|
CAG | C | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+5801_455+5802d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688935 | ||||||
| chr14:77689180
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.455+5558A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689180 | ||||||
| chr14:77689262
|
C | T | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.455+5476G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689262 | ||||||
| chr14:77689336
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.455+5402G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689336 | ||||||
| chr14:77689360
|
C | T | 17 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(14): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+5378G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689360 | ||||||
| chr14:77689688
|
AAC | A | 17 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(14): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+5048_455+5049d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689688 | ||||||
| chr14:77689818
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.455+4920C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689818 | ||||||
| chr14:77689846
|
T | TA | 25 | a0001c0001t0001g0178a0001c0001t0002g0022a0001c0001t0002g0023others(22): Show | 27 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.455+4891dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689846 | ||||||
| chr14:77689922
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.455+4816C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689922 | ||||||
| chr14:77690144
|
G | A | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.455+4594C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690144 | ||||||
| chr14:77690236
|
A | T | 1 | a0001c0001t0001g0178 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.455+4502T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690236 | ||||||
| chr14:77690314
|
A | C | 119 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(116): Show | 145 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.455+4424T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690314 | ||||||
| chr14:77690753
|
AT | A | 22 | a0001c0001t0001g0202a0001c0001t0002g0022a0001c0001t0002g0023others(19): Show | 24 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.455+3984delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690753 | ||||||
| chr14:77690806
|
CT | C | 6 | a0001c0001t0001g0172a0001c0001t0001g0201a0001c0001t0001g0202others(3): Show | 6 | HG02004.hp1 HG02004.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.455+3931delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690806 | ||||||
| chr14:77690843
|
C | T | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.455+3895G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690843 | ||||||
| chr14:77690863
|
G | A | 4 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0259others(1): Show | 7 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.455+3875C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690863 | ||||||
| chr14:77691025
|
T | C | 17 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(14): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+3713A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691025 | ||||||
| chr14:77691048
|
A | C | 1 | a0001c0001t0002g0165 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.455+3690T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691048 | ||||||
| chr14:77691142
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.455+3596G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691142 | ||||||
| chr14:77691223
|
T | A | 1 | a0001c0001t0003g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.455+3515A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691223 | ||||||
| chr14:77691448
|
G | A | 118 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(115): Show | 144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.455+3290C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691448 | ||||||
| chr14:77691540
|
A | C | 1 | a0002c0002t0004g0069 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.455+3198T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691540 | ||||||
| chr14:77691628
|
T | C | 1 | a0008c0010t0004g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.455+3110A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691628 | ||||||
| chr14:77691657
|
C | A | 8 | a0002c0002t0004g0070a0002c0002t0004g0074a0002c0002t0004g0075others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.455+3081G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691657 | ||||||
| chr14:77691674
|
C | T | 2 | a0001c0001t0002g0229a0001c0001t0002g0242 | 2 | NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.455+3064G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691674 | ||||||
| chr14:77691720
|
A | C | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.455+3018T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691720 | ||||||
| chr14:77691733
|
T | C | 1 | a0002c0002t0004g0089 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.455+3005A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691733 | ||||||
| chr14:77691816
|
A | G | 2 | a0001c0001t0003g0102a0001c0001t0003g0113 | 2 | HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.455+2922T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691816 | ||||||
| chr14:77691847
|
G | A | 12 | a0002c0003t0006g0010a0002c0003t0006g0021a0002c0003t0006g0051others(9): Show | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.455+2891C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691847 | ||||||
| chr14:77691908
|
C | T | 1 | a0001c0001t0002g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.455+2830G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691908 | ||||||
| chr14:77691912
|
C | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0203 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.455+2826G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77691912 | ||||||
| chr14:77692044
|
C | A | 1 | a0001c0001t0003g0120 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.455+2694G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692044 | ||||||
| chr14:77692104
|
C | T | 12 | a0002c0003t0006g0010a0002c0003t0006g0021a0002c0003t0006g0051others(9): Show | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.455+2634G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692104 | ||||||
| chr14:77692386
|
A | G | 85 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(82): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.455+2352T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692386 | ||||||
| chr14:77692602
|
T | C | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.455+2136A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692602 | ||||||
| chr14:77692796
|
G | GTATT | 62 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(59): Show | 84 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.455+1938_455+1941d others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692796 | ||||||
| chr14:77692813
|
T | C | 1 | a0001c0001t0005g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.455+1925A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692813 | ||||||
| chr14:77692862
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | NA19066.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.455+1876C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692862 | ||||||
| chr14:77692905
|
T | TAA | 28 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0148others(25): Show | 30 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.455+1831_455+1832d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692905 | ||||||
| chr14:77692916
|
A | AAT | 89 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0044others(86): Show | 113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.455+1821_455+1822i others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692916 | ||||||
| chr14:77692916
|
A | T | 4 | a0001c0001t0002g0060a0001c0001t0005g0260a0001c0001t0005g0261others(1): Show | 4 | HG02257.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.455+1822T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692916 | ||||||
| chr14:77692923
|
T | G | 1 | a0001c0001t0002g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.455+1815A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692923 | ||||||
| chr14:77692996
|
G | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.455+1742C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77692996 | ||||||
| chr14:77693131
|
G | A | 60 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(57): Show | 79 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.455+1607C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693131 | ||||||
| chr14:77693224
|
A | AAAC | 17 | a0002c0002t0004g0070a0002c0002t0004g0074a0002c0002t0004g0075others(14): Show | 20 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.455+1513_455+1514i others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693224 | ||||||
| chr14:77693224
|
A | AAAT | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+1513_455+1514i others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693224 | ||||||
| chr14:77693224
|
A | AATT | 56 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(53): Show | 74 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.455+1513_455+1514i others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693224 | ||||||
| chr14:77693224
|
A | ACAAC | 17 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(14): Show | 19 | HG00323.hp2 HG01167.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.455+1513_455+1514i others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693224 | ||||||
| chr14:77693224
|
A | AT | 8 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG02572.hp1 HG02738.hp1 HG03654.hp2 others(5): Show |
intron_variant | MODIFIER | c.455+1513dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693224 | ||||||
| chr14:77693224
|
A | C | 1 | a0002c0003t0006g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.455+1514T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693224 | ||||||
| chr14:77693224
|
A | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(109): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.455+1514T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693224 | ||||||
| chr14:77693252
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.455+1486A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693252 | ||||||
| chr14:77693275
|
C | CA | 53 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(50): Show | 72 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.455+1462dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693275 | ||||||
| chr14:77693294
|
T | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.455+1444A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693294 | ||||||
| chr14:77693388
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.455+1350T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693388 | ||||||
| chr14:77693398
|
T | C | 1 | a0001c0001t0003g0122 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.455+1340A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693398 | ||||||
| chr14:77693417
|
G | C | 1 | a0001c0001t0002g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.455+1321C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693417 | ||||||
| chr14:77693420
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0178 | 3 | NA18963.hp2 NA18979.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.455+1318T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693420 | ||||||
| chr14:77693448
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.455+1290T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693448 | ||||||
| chr14:77693472
|
C | A | 4 | a0001c0001t0002g0222a0001c0001t0002g0224a0001c0001t0002g0246others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.455+1266G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693472 | ||||||
| chr14:77693591
|
C | A | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.455+1147G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693591 | ||||||
| chr14:77693739
|
G | A | 21 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0046others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.455+999C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693739 | ||||||
| chr14:77693772
|
G | C | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.455+966C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693772 | ||||||
| chr14:77693814
|
C | T | 2 | a0002c0003t0006g0129a0002c0003t0009g0130 | 2 | HG03710.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.455+924G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693814 | ||||||
| chr14:77693823
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.455+915G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693823 | ||||||
| chr14:77693922
|
G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.455+816C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693922 | ||||||
| chr14:77693929
|
G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(51): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.455+809C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77693929 | ||||||
| chr14:77694044
|
T | C | 6 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(3): Show | 8 | HG01884.hp2 HG02165.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.455+694A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77694044 | ||||||
| chr14:77694081
|
G | T | 1 | a0001c0001t0005g0264 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.455+657C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77694081 | ||||||
| chr14:77694209
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(244): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.455+529G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77694209 | ||||||
| chr14:77694253
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.455+485A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77694253 | ||||||
| chr14:77694432
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.455+306A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77694432 | ||||||
| chr14:77694474
|
T | C | 6 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.455+264A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77694474 | ||||||
| chr14:77694648
|
T | G | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.455+90A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77694648 | ||||||
| chr14:77695007
|
A | G | 1 | a0001c0001t0003g0112 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.293-107T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695007 | ||||||
| chr14:77695028
|
G | C | 6 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(3): Show | 6 | HG02145.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-128C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695028 | ||||||
| chr14:77695095
|
G | A | 1 | a0001c0001t0003g0092 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.293-195C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695095 | ||||||
| chr14:77695163
|
T | C | 51 | a0001c0001t0001g0042a0001c0001t0003g0001a0001c0001t0003g0009others(48): Show | 70 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.293-263A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695163 | ||||||
| chr14:77695210
|
C | T | 2 | a0001c0001t0005g0262a0001c0001t0005g0270 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.293-310G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695210 | ||||||
| chr14:77695253
|
T | C | 1 | a0002c0002t0004g0079 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.293-353A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695253 | ||||||
| chr14:77695568
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.293-668C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695568 | ||||||
| chr14:77695685
|
G | C | 1 | a0001c0001t0003g0107 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.293-785C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695685 | ||||||
| chr14:77695701
|
AG | A | 100 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(97): Show | 124 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.293-802delC | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695701 | ||||||
| chr14:77695802
|
G | C | 1 | a0001c0001t0003g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.293-902C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695802 | ||||||
| chr14:77695817
|
G | A | 21 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(18): Show | 23 | HG00323.hp1 HG00323.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-917C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695817 | ||||||
| chr14:77695869
|
C | T | 1 | a0001c0001t0005g0260 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.293-969G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695869 | ||||||
| chr14:77695914
|
G | A | 2 | a0001c0001t0005g0262a0001c0001t0005g0270 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.293-1014C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695914 | ||||||
| chr14:77695996
|
G | C | 55 | a0001c0001t0001g0042a0001c0001t0003g0001a0001c0001t0003g0009others(52): Show | 74 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.293-1096C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77695996 | ||||||
| chr14:77696183
|
T | A | 1 | a0001c0001t0005g0269 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293-1283A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696183 | ||||||
| chr14:77696234
|
G | A | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-1334C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696234 | ||||||
| chr14:77696245
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.293-1345C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696245 | ||||||
| chr14:77696247
|
G | A | 9 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0259others(6): Show | 12 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.293-1347C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696247 | ||||||
| chr14:77696274
|
T | C | 100 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(97): Show | 124 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.293-1374A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696274 | ||||||
| chr14:77696372
|
T | C | 1 | a0001c0001t0005g0261 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.293-1472A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696372 | ||||||
| chr14:77696406
|
T | G | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.293-1506A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696406 | ||||||
| chr14:77696535
|
A | T | 1 | a0001c0001t0003g0110 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.293-1635T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696535 | ||||||
| chr14:77696551
|
A | G | 1 | a0001c0001t0003g0109 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.293-1651T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696551 | ||||||
| chr14:77696637
|
G | A | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.293-1737C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696637 | ||||||
| chr14:77696676
|
A | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0168a0001c0001t0001g0175 | 3 | HG01168.hp1 HG02735.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.293-1776T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696676 | ||||||
| chr14:77696776
|
C | T | 98 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(95): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.293-1876G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77696776 | ||||||
| chr14:77697062
|
T | C | 1 | a0001c0001t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.293-2162A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697062 | ||||||
| chr14:77697080
|
T | C | 98 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(95): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.293-2180A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697080 | ||||||
| chr14:77697252
|
A | C | 1 | a0001c0001t0002g0015 | 3 | HG03471.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.293-2352T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697252 | ||||||
| chr14:77697379
|
C | T | 55 | a0001c0001t0001g0042a0001c0001t0003g0001a0001c0001t0003g0009others(52): Show | 74 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.293-2479G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697379 | ||||||
| chr14:77697508
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 139 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.293-2608C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697508 | ||||||
| chr14:77697553
|
A | T | 1 | a0001c0001t0001g0174 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.293-2653T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697553 | ||||||
| chr14:77697656
|
C | T | 1 | a0001c0001t0003g0108 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.293-2756G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697656 | ||||||
| chr14:77697697
|
T | TA | 41 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(38): Show | 44 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.293-2798dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697697 | ||||||
| chr14:77697697
|
T | TAAA | 49 | a0001c0001t0001g0042a0001c0001t0003g0001a0001c0001t0003g0009others(46): Show | 68 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.293-2800_293-2798d others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697697 | ||||||
| chr14:77697697
|
TA | T | 35 | a0001c0001t0001g0150a0001c0001t0001g0168a0001c0001t0001g0169others(32): Show | 37 | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.293-2798delT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697697 | ||||||
| chr14:77697698
|
A | T | 4 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(1): Show | 4 | HG02258.hp1 HG03654.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-2798T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697698 | ||||||
| chr14:77697699
|
A | T | 1 | a0001c0001t0002g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.293-2799T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697699 | ||||||
| chr14:77697710
|
A | C | 2 | a0001c0001t0008g0166a0001c0001t0008g0167 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.293-2810T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697710 | ||||||
| chr14:77697867
|
G | A | 8 | a0002c0002t0004g0070a0002c0002t0004g0074a0002c0002t0004g0075others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-2967C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697867 | ||||||
| chr14:77697943
|
G | A | 5 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0071others(2): Show | 7 | HG02165.hp1 NA18954.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-3043C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697943 | ||||||
| chr14:77698012
|
A | G | 2 | a0003c0004t0006g0066a0003c0004t0006g0067 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.293-3112T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77698012 | ||||||
| chr14:77698034
|
A | T | 1 | a0001c0001t0003g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.293-3134T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77698034 | ||||||
| chr14:77698280
|
A | T | 1 | a0001c0001t0002g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.293-3380T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77698280 | ||||||
| chr14:77698583
|
G | A | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 126 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.293-3683C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77698583 | ||||||
| chr14:77698851
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.293-3951G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77698851 | ||||||
| chr14:77698874
|
G | A | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.293-3974C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77698874 | ||||||
| chr14:77699020
|
G | T | 1 | a0001c0001t0005g0259 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.293-4120C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699020 | ||||||
| chr14:77699021
|
C | T | 15 | a0001c0001t0002g0006a0001c0001t0002g0017a0001c0001t0002g0054others(12): Show | 19 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-4121G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699021 | ||||||
| chr14:77699024
|
C | T | 1 | a0001c0001t0002g0274 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.293-4124G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699024 | ||||||
| chr14:77699025
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293-4125C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699025 | ||||||
| chr14:77699264
|
T | G | 1 | a0002c0002t0004g0091 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.293-4364A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699264 | ||||||
| chr14:77699487
|
C | T | 9 | a0001c0001t0002g0006a0001c0001t0002g0060a0001c0001t0002g0061others(6): Show | 12 | HG01884.hp1 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-4587G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699487 | ||||||
| chr14:77699653
|
GACAA | G | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.292+4712_292+4715d others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699653 | ||||||
| chr14:77699696
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(244): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.292+4673G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699696 | ||||||
| chr14:77699784
|
G | A | 1 | a0001c0001t0003g0033 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.292+4585C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699784 | ||||||
| chr14:77699796
|
C | T | 1 | a0001c0001t0002g0226 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.292+4573G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699796 | ||||||
| chr14:77699828
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+4541C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699828 | ||||||
| chr14:77699838
|
A | C | 8 | a0002c0002t0004g0070a0002c0002t0004g0074a0002c0002t0004g0075others(5): Show | 8 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+4531T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699838 | ||||||
| chr14:77699851
|
A | C | 1 | a0001c0001t0002g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.292+4518T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699851 | ||||||
| chr14:77699851
|
A | G | 3 | a0001c0001t0002g0243a0001c0001t0003g0092a0001c0001t0003g0097 | 3 | HG01891.hp1 HG01978.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.292+4518T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699851 | ||||||
| chr14:77699861
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.292+4508A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699861 | ||||||
| chr14:77699872
|
A | G | 1 | a0002c0005t0004g0082 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.292+4497T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699872 | ||||||
| chr14:77699882
|
G | A | 3 | a0001c0001t0002g0061a0001c0001t0002g0254a0001c0001t0002g0255 | 3 | HG01884.hp1 HG02258.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.292+4487C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699882 | ||||||
| chr14:77699890
|
TA | T | 4 | a0001c0001t0002g0061a0001c0001t0002g0254a0001c0001t0013g0225others(1): Show | 4 | HG02258.hp1 HG02735.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+4478delT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699890 | ||||||
| chr14:77699911
|
T | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.292+4458A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699911 | ||||||
| chr14:77699915
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.292+4454G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77699915 | ||||||
| chr14:77700072
|
T | A | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292+4297A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700072 | ||||||
| chr14:77700074
|
A | T | 17 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0132others(14): Show | 19 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.292+4295T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700074 | ||||||
| chr14:77700076
|
A | T | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+4293T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700076 | ||||||
| chr14:77700078
|
T | A | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+4291A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700078 | ||||||
| chr14:77700113
|
C | T | 16 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0258others(13): Show | 19 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+4256G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700113 | ||||||
| chr14:77700490
|
T | G | 1 | a0001c0001t0003g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.292+3879A>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700490 | ||||||
| chr14:77700545
|
A | G | 4 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0148others(1): Show | 4 | HG03195.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+3824T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700545 | ||||||
| chr14:77700611
|
A | G | 135 | a0001c0001t0001g0042a0001c0001t0002g0022a0001c0001t0002g0023others(132): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.292+3758T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700611 | ||||||
| chr14:77700763
|
G | A | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | HG03654.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.292+3606C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700763 | ||||||
| chr14:77700814
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.292+3555T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700814 | ||||||
| chr14:77700935
|
T | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.292+3434A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700935 | ||||||
| chr14:77700939
|
A | T | 3 | a0001c0001t0002g0023a0001c0001t0002g0132a0001c0001t0002g0136 | 4 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+3430T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700939 | ||||||
| chr14:77701001
|
G | A | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+3368C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77701001 | ||||||
| chr14:77701043
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.292+3326G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77701043 | ||||||
| chr14:77701170
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.292+3199T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77701170 | ||||||
| chr14:77701354
|
G | C | 5 | a0001c0001t0002g0141a0001c0001t0002g0142a0001c0001t0002g0143others(2): Show | 5 | HG01081.hp1 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+3015C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77701354 | ||||||
| chr14:77701567
|
T | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.292+2802A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77701567 | ||||||
| chr14:77701900
|
T | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0245 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.292+2469A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77701900 | ||||||
| chr14:77702024
|
C | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.292+2345G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702024 | ||||||
| chr14:77702025
|
G | A | 12 | a0002c0003t0006g0010a0002c0003t0006g0021a0002c0003t0006g0051others(9): Show | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.292+2344C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702025 | ||||||
| chr14:77702286
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0212others(2): Show | 6 | HG01256.hp2 HG01433.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+2083C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702286 | ||||||
| chr14:77702355
|
G | A | 2 | a0001c0001t0005g0262a0001c0001t0005g0270 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.292+2014C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702355 | ||||||
| chr14:77702455
|
C | G | 3 | a0001c0001t0002g0015a0001c0001t0002g0251a0001c0001t0002g0252 | 5 | HG02922.hp2 HG03471.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+1914G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702455 | ||||||
| chr14:77702455
|
C | T | 1 | a0001c0001t0002g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.292+1914G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702455 | ||||||
| chr14:77702576
|
T | C | 4 | a0001c0001t0002g0222a0001c0001t0002g0224a0001c0001t0002g0246others(1): Show | 4 | HG02055.hp2 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+1793A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702576 | ||||||
| chr14:77702695
|
A | T | 3 | a0001c0001t0003g0096a0001c0001t0003g0103a0001c0001t0003g0104 | 3 | NA18979.hp1 NA18985.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.292+1674T>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702695 | ||||||
| chr14:77702886
|
G | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.292+1483C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702886 | ||||||
| chr14:77702905
|
A | C | 2 | a0001c0001t0005g0260a0001c0001t0005g0261 | 2 | HG02257.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.292+1464T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77702905 | ||||||
| chr14:77703012
|
C | T | 1 | a0001c0001t0003g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.292+1357G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703012 | ||||||
| chr14:77703275
|
G | A | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+1094C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703275 | ||||||
| chr14:77703316
|
T | C | 98 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(95): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.292+1053A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703316 | ||||||
| chr14:77703325
|
G | T | 5 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0062others(2): Show | 5 | HG01884.hp1 HG02258.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+1044C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703325 | ||||||
| chr14:77703384
|
C | T | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.292+985G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703384 | ||||||
| chr14:77703574
|
C | A | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.292+795G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703574 | ||||||
| chr14:77703593
|
C | CT | 28 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(25): Show | 30 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.292+775dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703593 | ||||||
| chr14:77703593
|
C | CTT | 7 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(4): Show | 7 | HG02071.hp2 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+774_292+775dup others(2): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703593 | ||||||
| chr14:77703593
|
C | CTTTT | 43 | a0001c0001t0001g0042a0001c0001t0003g0001a0001c0001t0003g0019others(40): Show | 59 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.292+772_292+775dup others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703593 | ||||||
| chr14:77703593
|
C | CTTTTT | 10 | a0001c0001t0003g0009a0001c0001t0003g0018a0001c0001t0003g0031others(7): Show | 13 | HG01175.hp1 HG01243.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.292+771_292+775dup others(5): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703593 | ||||||
| chr14:77703593
|
CTTTTTTT | C | 37 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(34): Show | 42 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.292+769_292+775del others(7): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703593 | ||||||
| chr14:77703660
|
C | T | 55 | a0001c0001t0001g0042a0001c0001t0003g0001a0001c0001t0003g0009others(52): Show | 74 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.292+709G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703660 | ||||||
| chr14:77703726
|
T | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.292+643A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703726 | ||||||
| chr14:77703760
|
G | A | 61 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(58): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.292+609C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703760 | ||||||
| chr14:77703786
|
C | T | 1 | a0002c0002t0004g0071 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.292+583G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703786 | ||||||
| chr14:77703799
|
T | C | 2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.292+570A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703799 | ||||||
| chr14:77703812
|
C | A | 1 | a0001c0001t0001g0042 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.292+557G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703812 | ||||||
| chr14:77704223
|
T | C | 1 | a0001c0001t0002g0145 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292+146A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77704223 | ||||||
| chr14:77704298
|
T | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.292+71A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77704298 | ||||||
| chr14:77704533
|
G | A | 1 | a0002c0002t0004g0070 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.184-56C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77704533 | ||||||
| chr14:77704553
|
C | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(235): Show | 310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.184-76G>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77704553 | ||||||
| chr14:77704726
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.184-249G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77704726 | ||||||
| chr14:77704884
|
T | A | 98 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(95): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.184-407A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77704884 | ||||||
| chr14:77705082
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.184-605G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705082 | ||||||
| chr14:77705285
|
C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0134 | 3 | HG01109.hp1 HG01243.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.184-808G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705285 | ||||||
| chr14:77705408
|
TAA | T | 7 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(4): Show | 7 | HG02015.hp2 NA18946.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-933_184-932del others(2): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705408 | ||||||
| chr14:77705409
|
A | G | 92 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(89): Show | 116 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.184-932T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705409 | ||||||
| chr14:77705411
|
GA | G | 66 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(63): Show | 85 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.184-935delT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705411 | ||||||
| chr14:77705411
|
GAA | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(118): Show | 163 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.184-936_184-935del others(2): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705411 | ||||||
| chr14:77705411
|
GAAA | G | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(7): Show | 10 | HG01070.hp2 HG01168.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.184-937_184-935del others(3): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705411 | ||||||
| chr14:77705411
|
GAAAA | G | 3 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0259 | 6 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-938_184-935del others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705411 | ||||||
| chr14:77705413
|
A | G | 7 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(4): Show | 7 | HG02015.hp2 NA18946.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-936T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705413 | ||||||
| chr14:77705499
|
C | T | 135 | a0001c0001t0001g0042a0001c0001t0002g0022a0001c0001t0002g0023others(132): Show | 164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.184-1022G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705499 | ||||||
| chr14:77705549
|
T | C | 3 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250 | 3 | NA18940.hp2 NA18982.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.184-1072A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705549 | ||||||
| chr14:77705626
|
T | C | 1 | a0001c0001t0002g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.184-1149A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705626 | ||||||
| chr14:77705751
|
C | T | 2 | a0001c0001t0003g0093a0001c0001t0003g0094 | 2 | HG02015.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.184-1274G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705751 | ||||||
| chr14:77705797
|
G | A | 61 | a0001c0001t0001g0042a0001c0001t0002g0044a0001c0001t0002g0045others(58): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.184-1320C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77705797 | ||||||
| chr14:77706046
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.184-1569G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706046 | ||||||
| chr14:77706080
|
T | C | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.184-1603A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706080 | ||||||
| chr14:77706104
|
C | CAT | 52 | a0001c0001t0003g0001a0001c0001t0003g0009a0001c0001t0003g0018others(49): Show | 71 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.184-1628_184-1627i others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706104 | ||||||
| chr14:77706104
|
C | CATAT | 21 | a0001c0001t0003g0092a0002c0002t0004g0074a0002c0002t0004g0075others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.184-1628_184-1627i others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706104 | ||||||
| chr14:77706104
|
C | CATATAT | 6 | a0002c0002t0004g0008a0002c0002t0004g0069a0002c0002t0004g0070others(3): Show | 8 | HG01109.hp2 HG02165.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-1628_184-1627i others(8): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706104 | ||||||
| chr14:77706106
|
C | CAT | 21 | a0001c0001t0001g0042a0001c0001t0001g0256a0001c0001t0001g0257others(18): Show | 23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.184-1631_184-1630d others(4): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706106 | ||||||
| chr14:77706106
|
C | CATAT | 12 | a0002c0003t0006g0010a0002c0003t0006g0021a0002c0003t0006g0051others(9): Show | 15 | HG01257.hp2 HG01258.hp2 HG03710.hp2 others(12): Show |
intron_variant | MODIFIER | c.184-1633_184-1630d others(6): Show |
ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706106 | ||||||
| chr14:77706106
|
C | T | 85 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0048others(82): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.184-1629G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706106 | ||||||
| chr14:77706108
|
T | C | 13 | a0001c0001t0001g0216a0001c0001t0002g0015a0001c0001t0002g0017others(10): Show | 16 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.184-1631A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706108 | ||||||
| chr14:77706178
|
A | C | 3 | a0003c0004t0006g0066a0003c0004t0006g0067a0003c0004t0006g0068 | 3 | HG01257.hp2 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.183+1644T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706178 | ||||||
| chr14:77706201
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.183+1621T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706201 | ||||||
| chr14:77706264
|
A | G | 6 | a0001c0001t0002g0017a0001c0001t0002g0054a0001c0001t0002g0055others(3): Show | 7 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.183+1558T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706264 | ||||||
| chr14:77706332
|
A | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 147 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.183+1490T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706332 | ||||||
| chr14:77706427
|
C | T | 1 | a0001c0001t0005g0258 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.183+1395G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706427 | ||||||
| chr14:77706527
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.183+1295A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706527 | ||||||
| chr14:77706684
|
T | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(85): Show | 127 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.183+1138A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706684 | ||||||
| chr14:77706742
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.183+1080C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706742 | ||||||
| chr14:77706914
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.183+908G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706914 | ||||||
| chr14:77706949
|
T | C | 2 | a0001c0001t0003g0029a0001c0001t0003g0219 | 3 | NA18989.hp1 NA19007.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.183+873A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706949 | ||||||
| chr14:77706964
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.183+858G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77706964 | ||||||
| chr14:77707059
|
A | G | 1 | a0002c0003t0006g0051 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.183+763T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707059 | ||||||
| chr14:77707149
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.183+673A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707149 | ||||||
| chr14:77707277
|
C | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.183+545G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707277 | ||||||
| chr14:77707279
|
G | C | 2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.183+543C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707279 | ||||||
| chr14:77707365
|
C | T | 3 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | HG02145.hp2 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.183+457G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707365 | ||||||
| chr14:77707397
|
G | A | 2 | a0001c0001t0001g0256a0001c0001t0001g0257 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.183+425C>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707397 | ||||||
| chr14:77707405
|
T | C | 16 | a0001c0001t0005g0016a0001c0001t0005g0030a0001c0001t0005g0258others(13): Show | 19 | HG00140.hp2 HG00280.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.183+417A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707405 | ||||||
| chr14:77707606
|
C | A | 1 | a0001c0001t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.183+216G>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707606 | ||||||
| chr14:77707606
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.183+216G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707606 | ||||||
| chr14:77707623
|
C | T | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0011g0043 | 3 | HG02559.hp2 HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.183+199G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707623 | ||||||
| chr14:77707649
|
C | T | 12 | a0001c0001t0001g0042a0001c0001t0003g0031a0001c0001t0003g0032others(9): Show | 12 | HG00408.hp2 HG01928.hp1 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.183+173G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707649 | ||||||
| chr14:77707759
|
G | C | 1 | a0008c0010t0004g0273 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.183+63C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707759 | ||||||
| chr14:77707818
|
G | C | 1 | a0001c0001t0002g0274 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.183+4C>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 1/5 | chr14 | 77707818 |