Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0002 | 0/0 | 389 | 38 | 4 | 10 | 17 | 3 | 4 | 16 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0003 | 0/0 | 389 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0004 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0005 | 0/0 | 389 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0006 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0007 | 0/0 | 389 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0008 | 0/0 | 389 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| a0009 | 0/0 | 389 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | MGKMA others(384): Show |
chr14 | 77667404 | 77713023 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1167 | 312 | 86 | 46 | 141 | 12 | 25 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0001c0011 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0002c0002 | 0/0 | 1167 | 24 | 2 | 10 | 7 | 2 | 3 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0002c0003 | 0/0 | 1167 | 12 | 0 | 0 | 10 | 1 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0002c0005 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0003c0004 | 0/0 | 1167 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0004c0007 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0005c0008 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0006c0010 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0007c0009 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0008c0012 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
chr14 | 77667404 | 77713023 | ||
| a0009c0006 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | ATGGG others(1162): Show |
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 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0002 | 1/1 | 2597 | 96 | 53 | 5 | 26 | 2 | 8 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0003 | 0/0 | 2597 | 71 | 9 | 11 | 46 | 1 | 4 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0005 | 0/0 | 2597 | 19 | 12 | 3 | 0 | 4 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0007 | 0/0 | 2598 | 5 | 0 | 0 | 5 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2593): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0008 | 0/0 | 2597 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0010 | 0/0 | 2597 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0011 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0013 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0001t0014 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0001c0011t0003 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0002c0002t0004 | 0/0 | 2597 | 24 | 2 | 10 | 7 | 2 | 3 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0002c0003t0006 | 0/0 | 2597 | 11 | 0 | 0 | 10 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0002c0003t0009 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0002c0005t0004 | 0/0 | 2597 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0003c0004t0006 | 0/0 | 2597 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0004c0007t0012 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0005c0008t0001 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0006c0010t0004 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0007c0009t0001 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0008c0012t0001 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
chr14 | 77667404 | 77713023 |
| a0009c0006t0001 | 0/0 | 2597 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | AGAGG others(2592): Show |
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 | 1 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0206 | 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 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0271 | 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 |
| 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 |
| a0001c0001t0002g0051 | 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 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 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 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0232 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0273 | 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 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 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 | 1 | 0 | 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 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0038 | 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 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0003g0220 | 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 |
| a0001c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 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 | 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 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0010g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0011g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0013g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0001c0001t0014g0036 | 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 |
| a0002c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0002t0004g0092 | 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 |
| a0002c0003t0006g0052 | 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 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0003t0009g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0005t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0002c0005t0004g0089 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0003c0004t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0004c0007t0012g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0005c0008t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0006c0010t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0007c0009t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0008c0012t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| a0009c0006t0001g0060 | 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 | g0140 | EUR | FIN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00323 | hp1 | a0002 | c0002 | t0004 | g0075 | EUR | FIN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00323 | hp2 | a0002 | c0002 | t0004 | g0081 | 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 | g0036 | 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 | g0181 | 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 | g0177 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0187 | 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 | g0180 | 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 | g0188 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00738 | hp2 | a0002 | c0002 | t0004 | g0078 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG00741 | hp2 | a0002 | c0002 | t0004 | g0084 | 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 | g0270 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0153 | 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 | g0189 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0145 | 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 | g0175 | 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 | g0161 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0071 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01167 | hp1 | a0002 | c0002 | t0004 | g0076 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01167 | hp2 | a0002 | c0002 | t0004 | g0086 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01168 | hp2 | a0002 | c0002 | t0004 | g0077 | 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 | g0029 | 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 | g0067 | 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 | g0068 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0258 | 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 | g0211 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01496 | hp1 | a0002 | c0002 | t0004 | g0092 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01496 | hp2 | a0002 | c0002 | t0004 | g0080 | AMR | CLM | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0031 | 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 | g0134 | 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 | g0031 | 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 | g0254 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01884 | hp2 | a0002 | c0002 | t0004 | g0091 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01934 | hp2 | a0002 | c0002 | t0004 | g0079 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0054 | 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 | g0213 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0095 | 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 | g0199 | 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 | g0223 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0271 | 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 | g0197 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0182 | 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 | g0049 | 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 | g0234 | EAS | CDX | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02165 | hp1 | a0002 | c0002 | t0004 | g0072 | 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 | g0260 | 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 | g0253 | 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 | g0212 | 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 | g0195 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02293 | hp2 | a0002 | c0002 | t0004 | g0088 | AMR | PEL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0266 | 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 | g0268 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0137 | 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 | g0090 | 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 | g0147 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02630 | hp1 | a0002 | c0002 | t0004 | g0085 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0167 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0245 | 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 | g0148 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02735 | hp2 | a0001 | c0001 | t0013 | g0224 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02738 | hp1 | a0005 | c0008 | t0001 | g0207 | 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 | g0045 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0263 | 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 | g0166 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0267 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0257 | 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 | g0246 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03195 | hp2 | a0006 | c0010 | t0004 | g0272 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0150 | 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 | g0264 | AFR | MSL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03486 | hp1 | a0002 | c0005 | t0004 | g0089 | 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 | g0146 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ESN | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0136 | 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 | g0063 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03688 | hp2 | a0002 | c0002 | t0004 | g0082 | 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 | g0201 | 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 | g0131 | SAS | PJL | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0178 | 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 | g0184 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04228 | hp1 | a0007 | c0009 | t0001 | g0216 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG04228 | hp2 | a0002 | c0002 | t0004 | g0087 | SAS | STU | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0044 | 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 | g0038 | EAS | CHB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0066 | 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 | g0160 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0248 | 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 | g0209 | 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 | g0128 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18947 | hp1 | a0002 | c0003 | t0006 | g0132 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0225 | 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 | g0203 | 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 | g0191 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0040 | 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 | g0070 | 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 | g0240 | 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 | a0008 | c0012 | t0001 | g0214 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0235 | 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 | g0200 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0194 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0236 | 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 | g0163 | 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 | g0126 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0228 | 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 | g0227 | 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 | g0218 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0185 | 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 | g0154 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18994 | hp1 | a0002 | c0003 | t0006 | g0129 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18994 | hp2 | a0002 | c0002 | t0004 | g0073 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18995 | hp2 | a0002 | c0002 | t0004 | g0074 | 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 | g0192 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0239 | 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 | g0033 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0179 | 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 | g0030 | 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 | g0219 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0168 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0193 | 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 | g0190 | 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 | g0186 | 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 | g0206 | 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 | g0165 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0162 | 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 | g0052 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0032 | 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 | g0230 | 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 | g0183 | EAS | JPT | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0039 | 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 | g0221 | AFR | YRI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ASW | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0215 | 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 | g0130 | EUR | TSI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20805 | hp1 | a0003 | c0004 | t0006 | g0069 | EUR | TSI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20905 | hp1 | a0009 | c0006 | t0001 | g0060 | SAS | GIH | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0226 | 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 | g0057 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02486 | hp1 | a0004 | c0007 | t0012 | g0058 | 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 | g0244 | AFR | ACB | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0046 | 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 | g0269 | 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 | g0047 | AFR | USA | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0252 | 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 | g0083 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | LWK | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0139 | REF | REF | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0232 | REF | REF | ALKBH1_chr14_77667404_77713023 | ALKBH1 | chr14 | 77667404 | 77713023 |
| view | 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 | a0007 | 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 | a0006 | 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 | a0002 a0003 a0006 |
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 | a0005 | 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 | a0004 | 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 | a0009 | 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 | a0008 | 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 |
| view | 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 | a0002c0002 a0002c0005 a0006c0010 |
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 |
| view | 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 | a0004c0007t0012 | 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 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(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 | a0002c0002t0004 a0002c0003t0006 a0002c0003t0009 others(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 | a0001c0001t0003 a0001c0001t0014 a0001c0011t0003 |
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 | a0002c0003t0006 a0002c0003t0009 a0003c0004t0006 |
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 |
| view | 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 | a0002c0002t0004g0088 | 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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): 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 | a0002c0002t0004g0081 a0002c0002t0004g0082 a0002c0002t0004g0085 others(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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0001g0181 | 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 | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(229): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): 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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): 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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0257 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0001g0195 | 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 | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.740+256A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675400 | |||||||
| chr14:77675433 | C | CA | 63 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(60): Show |
70 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.740+222dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675433 | |||||||
| chr14:77675515 | A | G | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.740+141T>C | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 5/5 | chr14 | 77675515 | |||||||
| chr14:77675998 | C | CT | 27 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(24): Show |
29 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.547-150dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77675998 | |||||||
| chr14:77675998 | C | CTT | 14 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0196 a0001c0001t0001g0203 others(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 | a0001c0001t0002g0243 | 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 | a0001c0001t0005g0259 a0001c0001t0005g0260 |
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 | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.547-314delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77676162 | |||||||
| chr14:77676278 | C | G | 25 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0002c0002t0004g0091 | 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 | a0001c0001t0003g0093 | 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 | a0001c0001t0002g0136 a0001c0001t0002g0141 |
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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0002g0221 | 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0002g0226 a0002c0002t0004g0008 a0002c0002t0004g0070 others(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 | a0001c0001t0002g0243 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0002g0061 | 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 | a0001c0001t0002g0007 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | 98 | a0001c0001t0001g0005 a0001c0001t0001g0169 a0001c0001t0001g0209 others(95): Show |
120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): 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 | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(81): 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 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0158 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0270 |
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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.546+1648G>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 4/5 | chr14 | 77678232 | |||||||
| chr14:77678233 | G | A | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): 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 | a0001c0001t0002g0023 a0001c0001t0002g0133 a0001c0001t0002g0137 |
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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(84): 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 | a0002c0002t0004g0085 | 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 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0053 others(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 | 52 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(49): Show |
71 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(68): 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 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(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 | a0002c0003t0006g0010 a0002c0003t0006g0021 a0002c0003t0006g0052 others(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 | a0001c0001t0001g0197 | 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 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0118 |
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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | 80 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(77): Show |
101 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(98): 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 | a0001c0001t0008g0168 | 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 | a0001c0001t0002g0249 | 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 | a0001c0001t0002g0049 | 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
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 | a0001c0001t0002g0062 | 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 | a0001c0001t0002g0249 | 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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0002g0149 a0001c0001t0002g0273 |
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 | a0001c0001t0001g0170 | 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 | 133 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(130): Show |
162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): 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 | a0001c0001t0002g0149 a0001c0001t0002g0273 |
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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | a0001c0001t0002g0231 | 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 | a0001c0001t0002g0166 | 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 | a0008c0012t0001g0214 | 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 | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(100): 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 | a0001c0001t0002g0166 | 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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0002c0002t0004g0071 a0002c0002t0004g0075 a0002c0002t0004g0076 others(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 | a0002c0002t0004g0072 a0002c0002t0004g0081 a0002c0002t0004g0082 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 others(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 | a0003c0004t0006g0068 | 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 | a0001c0001t0002g0050 | 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 | a0001c0001t0002g0049 | 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 |
8 | a0001c0001t0002g0023 a0001c0001t0002g0133 a0001c0001t0002g0134 others(5): Show |
9 | HG01516.hp1 HG01891.hp2 HG02572.hp2 others(6): 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 | a0001c0001t0002g0022 a0001c0001t0002g0140 a0001c0001t0002g0142 others(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 | a0001c0001t0002g0135 a0001c0001t0002g0143 |
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 | a0001c0001t0001g0155 a0001c0001t0002g0015 a0001c0001t0002g0221 others(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 | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): 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 | a0001c0001t0001g0155 a0001c0001t0002g0015 a0001c0001t0002g0221 others(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 | a0001c0001t0005g0263 | 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 | a0002c0003t0006g0132 | 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 | a0001c0001t0005g0262 | 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 | a0001c0001t0013g0224 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0054 others(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 | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): 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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0002c0003t0006g0010 a0002c0003t0006g0021 a0002c0003t0006g0052 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0002g0006 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0002c0002t0004g0088 | 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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0257 others(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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0257 others(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 | a0001c0001t0002g0136 | 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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | a0001c0001t0003g0038 a0001c0001t0003g0040 |
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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0001g0026 a0001c0001t0001g0152 a0001c0001t0001g0164 others(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 | a0001c0001t0002g0243 a0001c0001t0005g0265 a0001c0001t0005g0270 others(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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0151 a0001c0001t0001g0155 others(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 | 28 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(25): Show |
30 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(27): 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 others(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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): 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 | a0001c0001t0002g0007 a0001c0001t0002g0225 a0001c0001t0002g0227 others(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 | a0001c0001t0002g0061 | 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 | a0001c0001t0007g0160 | 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 | a0002c0002t0004g0081 a0002c0002t0004g0082 a0002c0002t0004g0085 others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0257 others(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 | a0001c0001t0005g0031 | 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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0003g0099 a0001c0001t0003g0114 |
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 | a0002c0002t0004g0092 | 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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.456-4354C>A | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77684324 | |||||||
| chr14:77684368 | CT | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): 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 | a0002c0003t0006g0010 a0002c0003t0006g0021 a0002c0003t0006g0052 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0001g0011 a0001c0001t0001g0151 a0001c0001t0001g0169 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0005g0257 a0001c0001t0005g0264 |
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 | a0001c0001t0005g0257 a0001c0001t0005g0264 |
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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0257 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | a0001c0001t0002g0273 | 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 | a0002c0002t0004g0071 a0002c0002t0004g0075 a0002c0002t0004g0076 others(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 | a0001c0001t0005g0257 a0001c0001t0005g0264 |
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 | a0002c0002t0004g0092 | 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.456-5467dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77685436 | |||||||
| chr14:77685450 | A | C | 26 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0002g0022 others(23): Show |
28 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(25): 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 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0002g0147 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0156 a0001c0001t0001g0173 others(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 | a0001c0001t0001g0187 a0001c0001t0001g0271 a0002c0003t0006g0010 others(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 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
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 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0149 others(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 | a0002c0002t0004g0085 | 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0003g0093 | 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 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0245 others(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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0001g0178 a0001c0001t0001g0184 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0002g0015 a0001c0001t0002g0250 a0001c0001t0002g0251 |
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 | a0001c0001t0005g0257 a0001c0001t0005g0264 |
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 | a0001c0001t0001g0186 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0159 | 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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0149 others(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 | a0001c0001t0002g0147 | 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 | 114 | a0001c0001t0002g0022 a0001c0001t0002g0045 a0001c0001t0002g0046 others(111): Show |
139 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(136): 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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0002g0144 | 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.455+7012A>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77687726 | |||||||
| chr14:77687790 | G | T | 57 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(54): Show |
64 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(61): 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 | a0001c0001t0002g0015 a0001c0001t0002g0221 a0001c0001t0002g0223 others(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 | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): 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 | a0001c0001t0002g0149 a0001c0001t0002g0273 |
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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0210 a0001c0001t0002g0047 a0001c0001t0002g0048 others(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 | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): 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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | 46 | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0163 others(43): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.455+6184dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77688553 | |||||||
| chr14:77688553 | CTTT | C | 52 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0001g0158 | 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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0007c0009t0001g0216 | 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 | a0001c0001t0002g0140 | 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 | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(85): 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 | a0001c0001t0002g0022 a0001c0001t0002g0135 a0001c0001t0002g0138 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): 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 | a0001c0001t0001g0156 | 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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0001c0001t0002g0063 | 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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0001c0001t0001g0201 | 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 | 24 | a0001c0001t0001g0179 a0001c0001t0002g0022 a0001c0001t0002g0023 others(21): Show |
26 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.455+4891dupT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77689846 | |||||||
| chr14:77689922 | G | A | 1 | a0001c0001t0002g0136 | 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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0001g0179 | 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 | 118 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(115): Show |
144 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.455+4424T>G | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690314 | |||||||
| chr14:77690753 | AT | A | 21 | a0001c0001t0001g0203 a0001c0001t0002g0022 a0001c0001t0002g0023 others(18): Show |
23 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.455+3984delA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 3/5 | chr14 | 77690753 | |||||||
| chr14:77690806 | CT | C | 6 | a0001c0001t0001g0173 a0001c0001t0001g0202 a0001c0001t0001g0203 others(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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0258 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0002g0065 | 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 | 117 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(114): Show |
143 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(140): 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 | a0002c0002t0004g0070 | 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 | a0006c0010t0004g0272 | 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 | a0002c0002t0004g0071 a0002c0002t0004g0075 a0002c0002t0004g0076 others(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 | a0001c0001t0002g0228 a0001c0001t0002g0241 |
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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0002c0002t0004g0090 | 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 | a0001c0001t0003g0102 a0001c0001t0003g0113 |
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 | a0002c0003t0006g0010 a0002c0003t0006g0021 a0002c0003t0006g0052 others(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 | |||||||
| chr14:77691912 | C | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0204 |
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 | a0002c0003t0006g0010 a0002c0003t0006g0021 a0002c0003t0006g0052 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0005g0263 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
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 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0149 others(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 | 88 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0045 others(85): Show |
112 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(109): 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 | a0001c0001t0002g0061 a0001c0001t0005g0259 a0001c0001t0005g0260 others(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 | a0001c0001t0002g0253 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0002c0002t0004g0071 a0002c0002t0004g0075 a0002c0002t0004g0076 others(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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0002c0003t0006g0130 | 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 | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0001c0001t0002g0134 | 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 | a0001c0001t0002g0246 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0179 |
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 | a0001c0001t0001g0178 | 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 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0245 others(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 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(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 | 20 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0047 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0002c0003t0006g0130 a0002c0003t0009g0131 |
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 | a0001c0001t0001g0177 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0001c0001t0005g0263 | 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 | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0003g0093 | 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 | a0001c0001t0001g0043 a0001c0001t0003g0001 a0001c0001t0003g0009 others(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 | a0001c0001t0005g0261 a0001c0001t0005g0269 |
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 | a0002c0002t0004g0080 | 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 | a0001c0001t0002g0149 | 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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0001c0001t0005g0259 | 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 | a0001c0001t0005g0261 a0001c0001t0005g0269 |
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 | a0001c0001t0001g0043 a0001c0001t0003g0001 a0001c0001t0003g0009 others(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 | a0001c0001t0005g0268 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(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 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0258 others(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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0005g0260 | 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0169 a0001c0001t0001g0176 |
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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0001g0043 a0001c0001t0003g0001 a0001c0001t0003g0009 others(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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): 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 | a0001c0001t0001g0175 | 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 | 40 | a0001c0001t0001g0028 a0001c0001t0001g0210 a0001c0001t0002g0049 others(37): 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 | a0001c0001t0001g0043 a0001c0001t0003g0001 a0001c0001t0003g0009 others(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 | 34 | a0001c0001t0001g0151 a0001c0001t0001g0169 a0001c0001t0001g0170 others(31): Show |
36 | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-2798delT | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77697697 | |||||||
| chr14:77697698 | A | T | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(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 | a0001c0001t0002g0254 | 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 | a0001c0001t0008g0167 a0001c0001t0008g0168 |
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 | a0002c0002t0004g0071 a0002c0002t0004g0075 a0002c0002t0004g0076 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0072 others(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 | a0003c0004t0006g0067 a0003c0004t0006g0068 |
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 | a0001c0001t0002g0138 | 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): 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 | a0001c0001t0002g0137 | 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 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
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 | a0001c0001t0005g0258 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0017 a0001c0001t0002g0055 others(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 | a0001c0001t0002g0273 | 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 | a0001c0001t0002g0147 | 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 | a0002c0002t0004g0092 | 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 | a0001c0001t0002g0006 a0001c0001t0002g0061 a0001c0001t0002g0062 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | 245 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(242): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): 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 | a0001c0001t0003g0041 | 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 | a0001c0001t0002g0225 | 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 | a0001c0001t0002g0254 | 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 | a0002c0002t0004g0071 a0002c0002t0004g0075 a0002c0002t0004g0076 others(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 | a0001c0001t0002g0047 | 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 | a0001c0001t0002g0242 a0001c0001t0003g0093 a0001c0001t0003g0097 |
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 | a0001c0001t0002g0242 | 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 | a0002c0005t0004g0083 | 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 | a0001c0001t0002g0062 a0001c0001t0002g0253 a0001c0001t0002g0254 |
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 | a0001c0001t0002g0062 a0001c0001t0002g0253 a0001c0001t0013g0224 others(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 | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): 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 | a0001c0001t0002g0055 | 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 | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.292+4297A>T | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77700072 | |||||||
| chr14:77700074 | A | T | 16 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0133 others(13): Show |
18 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(15): 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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0257 others(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 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0149 others(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 | 134 | a0001c0001t0001g0043 a0001c0001t0002g0022 a0001c0001t0002g0023 others(131): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): 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 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
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 | a0001c0001t0002g0273 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0001c0001t0002g0023 a0001c0001t0002g0133 a0001c0001t0002g0137 |
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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0002g0142 | 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 | a0001c0001t0002g0142 a0001c0001t0002g0143 a0001c0001t0002g0144 others(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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0002c0003t0006g0010 a0002c0003t0006g0021 a0002c0003t0006g0052 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0211 others(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 | a0001c0001t0005g0261 a0001c0001t0005g0269 |
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 | a0001c0001t0002g0015 a0001c0001t0002g0250 a0001c0001t0002g0251 |
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 | a0001c0001t0002g0253 | 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 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0002g0245 others(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 | a0001c0001t0003g0096 a0001c0001t0003g0103 a0001c0001t0003g0104 |
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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0005g0259 a0001c0001t0005g0260 |
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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | 27 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(24): Show |
29 | HG00280.hp2 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.292+775dupA | ALKBH1 | ENSG00000100601.10 | transcript | ENST00000216489.8 | protein_coding | 2/5 | chr14 | 77703593 | |||||||
| chr14:77703593 | C | CTT | 7 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0001g0043 a0001c0001t0003g0001 a0001c0001t0003g0019 others(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 | a0001c0001t0003g0009 a0001c0001t0003g0018 a0001c0001t0003g0032 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | a0001c0001t0001g0043 a0001c0001t0003g0001 a0001c0001t0003g0009 others(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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0002c0002t0004g0072 | 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 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
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 | a0001c0001t0001g0043 | 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 | a0001c0001t0002g0146 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0002c0002t0004g0071 | 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 | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0002g0221 | 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 | a0001c0001t0002g0022 a0001c0001t0002g0135 |
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 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(116): Show |
162 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(159): 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 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0258 |
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 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0041 others(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 | 134 | a0001c0001t0001g0043 a0001c0001t0002g0022 a0001c0001t0002g0023 others(131): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): 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 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 |
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 | a0001c0001t0002g0147 | 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 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
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 | a0001c0001t0001g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(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 | a0001c0001t0002g0149 | 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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0009 a0001c0001t0003g0018 others(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 | a0001c0001t0003g0093 a0002c0002t0004g0075 a0002c0002t0004g0076 others(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 | a0002c0002t0004g0008 a0002c0002t0004g0070 a0002c0002t0004g0071 others(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 | 20 | a0001c0001t0001g0043 a0001c0001t0001g0255 a0001c0001t0001g0256 others(17): Show |
22 | HG00280.hp2 HG01081.hp1 HG01109.hp1 others(19): 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 | a0002c0003t0006g0010 a0002c0003t0006g0021 a0002c0003t0006g0052 others(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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0049 others(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 | a0001c0001t0001g0215 a0001c0001t0002g0015 a0001c0001t0002g0017 others(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 | a0003c0004t0006g0067 a0003c0004t0006g0068 a0003c0004t0006g0069 |
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 | a0001c0001t0001g0150 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0055 a0001c0001t0002g0056 others(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 | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(100): 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 | a0001c0001t0005g0257 | 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 | a0001c0001t0001g0217 | 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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(84): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0003g0030 a0001c0001t0003g0218 |
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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0002c0003t0006g0052 | 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 | a0001c0001t0001g0219 | 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 | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(232): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): 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 | a0001c0001t0002g0253 a0001c0001t0002g0254 |
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 | a0001c0001t0002g0049 a0001c0001t0002g0050 a0001c0001t0002g0051 |
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 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
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 | a0001c0001t0005g0016 a0001c0001t0005g0031 a0001c0001t0005g0257 others(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 | a0001c0001t0001g0271 | 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 | a0001c0001t0002g0047 a0001c0001t0002g0048 |
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 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0011g0044 |
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 | a0001c0001t0001g0043 a0001c0001t0003g0032 a0001c0001t0003g0033 others(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 | a0006c0010t0004g0272 | 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 | a0001c0001t0002g0273 | 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 |