Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221120 |
| ensemblid | ENSG00000166199.13 |
| hgncid | 30141 |
| symbol | ALKBH3 |
| name | alkB homolog 3, alpha-ketoglutarate dependent dioxygenase |
| refseq_nuc | NM_139178.4 |
| refseq_prot | NP_631917.1 |
| ensembl_nuc | ENST00000302708.9 |
| ensembl_prot | ENSP00000302232.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 43880831 |
| end | 43920274 |
| strand | + |
| ver | v1.2 |
| region | chr11:43880831-43920274 |
| region5000 | chr11:43875831-43925274 |
| regionname0 | ALKBH3_chr11_43880831_43920274 |
| regionname5000 | ALKBH3_chr11_43875831_43925274 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 286 | 319 | 85 | 67 | 126 | 12 | 28 | 98 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | MEEKR others(281): Show |
chr11 | 43875831 | 43925274 |
| a0002 | 0/0 | 286 | 51 | 11 | 11 | 17 | 2 | 10 | 13 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | MEEKR others(281): Show |
chr11 | 43875831 | 43925274 |
| a0003 | 0/0 | 286 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | MEEKR others(281): Show |
chr11 | 43875831 | 43925274 |
| a0004 | 0/1 | 69 | 2 | 0 | 0 | 1 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | MEEKR others(64): Show |
chr11 | 43875831 | 43925274 |
| a0005 | 0/0 | 286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | MEEKR others(281): Show |
chr11 | 43875831 | 43925274 |
| a0006 | 0/0 | 286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | MEEKR others(281): Show |
chr11 | 43875831 | 43925274 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 858 | 196 | 22 | 34 | 107 | 9 | 24 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0001c0002 | 0/0 | 858 | 93 | 57 | 17 | 14 | 3 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0001c0004 | 0/0 | 858 | 27 | 5 | 15 | 5 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0001c0006 | 1/0 | 858 | 2 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0001c0007 | 0/0 | 858 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0002c0003 | 0/0 | 858 | 51 | 11 | 11 | 17 | 2 | 10 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0003c0005 | 0/0 | 858 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0004c0009 | 0/1 | 858 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0004c0010 | 0/0 | 858 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0005c0008 | 0/0 | 858 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 | ||
| a0006c0011 | 0/0 | 858 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ATGGA others(853): Show |
chr11 | 43875831 | 43925274 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1544 | 179 | 12 | 29 | 106 | 9 | 23 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0001t0005 | 0/0 | 1544 | 14 | 10 | 3 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0001t0008 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0001t0009 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0001t0010 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0002t0001 | 0/0 | 1544 | 40 | 15 | 9 | 14 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0002t0002 | 0/0 | 1544 | 15 | 13 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0002t0004 | 0/0 | 1544 | 25 | 18 | 6 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0002t0006 | 0/0 | 1544 | 8 | 6 | 0 | 0 | 2 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0002t0007 | 0/0 | 1544 | 5 | 5 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0004t0003 | 0/0 | 1544 | 27 | 5 | 15 | 5 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0006t0001 | 1/0 | 1544 | 2 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0001c0007t0005 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0002c0003t0002 | 0/0 | 1544 | 51 | 11 | 11 | 17 | 2 | 10 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0003c0005t0001 | 0/0 | 1544 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0004c0009t0001 | 0/1 | 1544 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0004c0010t0002 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0005c0008t0001 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| a0006c0011t0002 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | ACTCT others(1539): Show |
chr11 | 43875831 | 43925274 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 26 | 0 | 1 | 23 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0009g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0001t0010g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0002g0003 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0002g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0004g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0006g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0006g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0007g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0002t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0004 | 0/0 | 9 | 0 | 6 | 1 | 0 | 2 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0009 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0004t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0006t0001g0025 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0001c0007t0005g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0007 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0017 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0049 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0050 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0002c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0003c0005t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0004c0009t0001g0099 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0004c0010t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0005c0008t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| a0006c0011t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00140 | hp2 | a0001 | c0002 | t0006 | g0051 | EUR | GBR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00423 | hp2 | a0001 | c0004 | t0003 | g0004 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00438 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0012 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00609 | hp2 | a0001 | c0004 | t0003 | g0027 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00621 | hp1 | a0002 | c0003 | t0002 | g0018 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00639 | hp1 | a0001 | c0004 | t0003 | g0028 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0014 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00642 | hp1 | a0001 | c0004 | t0003 | g0060 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00642 | hp2 | a0002 | c0003 | t0002 | g0017 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0193 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG00741 | hp2 | a0002 | c0003 | t0002 | g0173 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0108 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01069 | hp2 | a0001 | c0004 | t0003 | g0063 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01071 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01074 | hp1 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01074 | hp2 | a0002 | c0003 | t0002 | g0179 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01081 | hp1 | a0001 | c0004 | t0003 | g0066 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01081 | hp2 | a0002 | c0003 | t0002 | g0048 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0059 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01168 | hp1 | a0001 | c0007 | t0005 | g0191 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01175 | hp1 | a0002 | c0003 | t0002 | g0185 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0058 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0058 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0150 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0186 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01358 | hp2 | a0001 | c0002 | t0004 | g0223 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01361 | hp1 | a0001 | c0004 | t0003 | g0065 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01361 | hp2 | a0002 | c0003 | t0002 | g0103 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0224 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01433 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0167 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01928 | hp2 | a0001 | c0004 | t0003 | g0009 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01934 | hp2 | a0001 | c0004 | t0003 | g0009 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01943 | hp1 | a0002 | c0003 | t0002 | g0166 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01952 | hp1 | a0001 | c0004 | t0003 | g0062 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01978 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01993 | hp1 | a0001 | c0004 | t0003 | g0009 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02004 | hp2 | a0002 | c0003 | t0002 | g0184 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02055 | hp2 | a0002 | c0003 | t0002 | g0049 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02135 | hp2 | a0002 | c0003 | t0002 | g0018 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02145 | hp2 | a0001 | c0002 | t0006 | g0187 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CDX | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02258 | hp1 | a0002 | c0003 | t0002 | g0047 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02258 | hp2 | a0001 | c0004 | t0003 | g0028 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02273 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02451 | hp2 | a0002 | c0003 | t0002 | g0047 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02572 | hp1 | a0001 | c0002 | t0006 | g0189 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02615 | hp2 | a0001 | c0004 | t0003 | g0064 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0211 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02630 | hp2 | a0002 | c0003 | t0002 | g0169 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02647 | hp1 | a0002 | c0003 | t0002 | g0176 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02683 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02698 | hp2 | a0002 | c0003 | t0002 | g0174 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02717 | hp2 | a0001 | c0002 | t0007 | g0215 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02723 | hp1 | a0005 | c0008 | t0001 | g0171 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0217 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0017 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0192 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02818 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02886 | hp1 | a0002 | c0003 | t0002 | g0165 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02886 | hp2 | a0001 | c0004 | t0003 | g0029 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02922 | hp2 | a0002 | c0003 | t0002 | g0050 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02970 | hp2 | a0001 | c0002 | t0006 | g0190 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0151 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03041 | hp1 | a0006 | c0011 | t0002 | g0149 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0212 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0052 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03139 | hp1 | a0001 | c0002 | t0007 | g0026 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03195 | hp2 | a0002 | c0003 | t0002 | g0007 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03225 | hp2 | a0001 | c0002 | t0007 | g0026 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0164 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03453 | hp1 | a0002 | c0003 | t0002 | g0168 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03491 | hp2 | a0001 | c0004 | t0003 | g0004 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03492 | hp1 | a0001 | c0004 | t0003 | g0004 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0172 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | ESN | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0052 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03654 | hp2 | a0002 | c0003 | t0002 | g0049 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0106 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0177 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03942 | hp2 | a0002 | c0003 | t0002 | g0017 | SAS | BEB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0183 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0203 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG04228 | hp2 | a0002 | c0003 | t0002 | g0181 | SAS | STU | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0025 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18939 | hp1 | a0002 | c0003 | t0002 | g0105 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18940 | hp1 | a0002 | c0003 | t0002 | g0018 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18942 | hp2 | a0002 | c0003 | t0002 | g0101 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18946 | hp2 | a0002 | c0003 | t0002 | g0104 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18947 | hp2 | a0003 | c0005 | t0001 | g0030 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18951 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18961 | hp1 | a0002 | c0003 | t0002 | g0102 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18964 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18972 | hp1 | a0002 | c0003 | t0002 | g0180 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18978 | hp2 | a0002 | c0003 | t0002 | g0178 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18983 | hp1 | a0001 | c0004 | t0003 | g0027 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18994 | hp2 | a0003 | c0005 | t0001 | g0030 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA18995 | hp2 | a0004 | c0010 | t0002 | g0033 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19030 | hp1 | a0001 | c0004 | t0003 | g0067 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0026 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0221 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19043 | hp2 | a0002 | c0003 | t0002 | g0175 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19056 | hp2 | a0001 | c0004 | t0003 | g0061 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19060 | hp1 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19063 | hp1 | a0001 | c0004 | t0003 | g0009 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19070 | hp1 | a0002 | c0003 | t0002 | g0050 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19089 | hp2 | a0002 | c0003 | t0002 | g0033 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19090 | hp2 | a0002 | c0003 | t0002 | g0018 | EAS | JPT | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | YRI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ASW | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ASW | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20752 | hp1 | a0002 | c0003 | t0002 | g0182 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0222 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20805 | hp2 | a0001 | c0002 | t0006 | g0051 | EUR | TSI | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | GIH | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01123 | hp1 | a0001 | c0004 | t0003 | g0004 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0195 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02109 | hp2 | a0001 | c0002 | t0006 | g0188 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0201 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ACB | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | MSL | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG06807 | hp1 | a0001 | c0002 | t0007 | g0216 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0208 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | USA | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | LWK | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| homoSapiens | chm13v2 | a0004 | c0009 | t0001 | g0099 | REF | REF | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0001 | g0025 | REF | REF | ALKBH3_chr11_43875831_43925274 | ALKBH3 | chr11 | 43875831 | 43925274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43883120 | G | T | 1 | a0006 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.115G>T | p.Gly39Cys | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/10 | 534/1544 | 115/861 | 39/286 | chr11 | 43883120 | |||
| chr11:43884007 | C | T | 1 | a0004 | 1 | NA18995.hp2 | stop_gained | HIGH | c.208C>T | p.Arg70* | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/10 | 627/1544 | 208/861 | 70/286 | chr11 | 43884007 | |||
| chr11:43892127 | C | G | 1 | a0005 | 1 | HG02723.hp1 | missense_variant&splice_region_variant | MODERATE | c.457C>G | p.His153Asp | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/10 | 876/1544 | 457/861 | 153/286 | chr11 | 43892127 | |||
| chr11:43901546 | C | T | 1 | a0003 | 2 | NA18947.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.490C>T | p.Arg164Cys | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/10 | 909/1544 | 490/861 | 164/286 | chr11 | 43901546 | |||
| chr11:43919052 | C | G | 2 | a0002 a0004 |
52 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
missense_variant | MODERATE | c.684C>G | p.Asp228Glu | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/10 | 1103/1544 | 684/861 | 228/286 | chr11 | 43919052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43883086 | T | G | 1 | a0001c0007 | 1 | HG01168.hp1 | splice_region_variant&synonymous_variant | LOW | c.81T>G | p.Ala27Ala | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/10 | 500/1544 | 81/861 | 27/286 | chr11 | 43883086 | |||
| chr11:43889815 | T | C | 9 | a0001c0001 a0001c0002 a0001c0004 others(6): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
synonymous_variant | LOW | c.357T>C | p.Thr119Thr | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/10 | 776/1544 | 357/861 | 119/286 | chr11 | 43889815 | |||
| chr11:43892054 | G | A | 1 | a0001c0004 | 27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
synonymous_variant | LOW | c.384G>A | p.Gln128Gln | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/10 | 803/1544 | 384/861 | 128/286 | chr11 | 43892054 | |||
| chr11:43919094 | G | T | 5 | a0001c0001 a0001c0004 a0001c0007 others(2): Show |
227 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(224): Show |
synonymous_variant | LOW | c.726G>T | p.Gly242Gly | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/10 | 1145/1544 | 726/861 | 242/286 | chr11 | 43919094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43880873 | C | T | 2 | a0001c0001t0005 a0001c0007t0005 |
15 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-377C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | chr11 | 43880873 | |||||||
| chr11:43880975 | T | C | 1 | a0001c0002t0006 | 8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-275T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1678 | chr11 | 43880975 | ||||||
| chr11:43881070 | G | A | 2 | a0001c0002t0007 a0001c0004t0003 |
32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-180G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1583 | chr11 | 43881070 | ||||||
| chr11:43881100 | G | A | 1 | a0001c0001t0008 | 1 | HG01069.hp1 | 5_prime_UTR_variant | MODIFIER | c.-150G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1553 | chr11 | 43881100 | ||||||
| chr11:43881131 | G | T | 1 | a0001c0002t0004 | 25 | HG00735.hp1 HG01167.hp1 HG01256.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-119G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/10 | 1522 | chr11 | 43881131 | ||||||
| chr11:43882598 | T | A | 1 | a0001c0001t0009 | 1 | HG00639.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-55T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/10 | chr11 | 43882598 | |||||||
| chr11:43920012 | G | A | 1 | a0001c0001t0010 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 10/10 | 2 | chr11 | 43920012 | ||||||
| chr11:43920087 | C | G | 1 | a0001c0002t0007 | 5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*77C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 10/10 | 77 | chr11 | 43920087 | ||||||
| chr11:43920227 | C | G | 4 | a0001c0002t0002 a0002c0003t0002 a0004c0010t0002 others(1): Show |
68 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*217C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 10/10 | 217 | chr11 | 43920227 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43881231 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-71+52C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881231 | |||||||
| chr11:43881286 | A | G | 6 | a0001c0002t0004g0058 a0001c0002t0004g0059 a0001c0002t0004g0221 others(3): Show |
8 | HG00735.hp1 HG01167.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71+107A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881286 | |||||||
| chr11:43881344 | G | A | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-71+165G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881344 | |||||||
| chr11:43881427 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG03927.hp2 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-71+248C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881427 | |||||||
| chr11:43881637 | C | T | 1 | a0001c0002t0004g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-71+458C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881637 | |||||||
| chr11:43881640 | C | T | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+461C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881640 | |||||||
| chr11:43881707 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-71+528G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881707 | |||||||
| chr11:43881778 | G | C | 8 | a0002c0003t0002g0033 a0002c0003t0002g0101 a0002c0003t0002g0102 others(5): Show |
8 | HG01361.hp2 HG03669.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+599G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881778 | |||||||
| chr11:43881828 | T | C | 16 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 others(13): Show |
32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.-71+649T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881828 | |||||||
| chr11:43881841 | T | G | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-71+662T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43881841 | |||||||
| chr11:43882050 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-70-533G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882050 | |||||||
| chr11:43882070 | T | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.-70-513T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882070 | |||||||
| chr11:43882167 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-70-416T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882167 | |||||||
| chr11:43882223 | A | T | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-70-360A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882223 | |||||||
| chr11:43882248 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-70-335G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882248 | |||||||
| chr11:43882292 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-70-291G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882292 | |||||||
| chr11:43882306 | A | G | 4 | a0001c0001t0005g0053 a0001c0001t0005g0192 a0001c0001t0005g0193 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-277A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882306 | |||||||
| chr11:43882520 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-70-63C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 1/9 | chr11 | 43882520 | |||||||
| chr11:43882741 | T | C | 1 | a0001c0001t0008g0108 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79+10T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/9 | chr11 | 43882741 | |||||||
| chr11:43882833 | C | T | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+102C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/9 | chr11 | 43882833 | |||||||
| chr11:43882903 | T | C | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79+172T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 2/9 | chr11 | 43882903 | |||||||
| chr11:43883196 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.183+8C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883196 | |||||||
| chr11:43883326 | GA | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(89): Show |
150 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.183+139delA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883326 | |||||||
| chr11:43883327 | A | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.183+139A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883327 | |||||||
| chr11:43883389 | C | A | 2 | a0001c0002t0004g0058 a0001c0002t0004g0221 |
3 | HG01256.hp2 HG01258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.183+201C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883389 | |||||||
| chr11:43883510 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.183+322A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883510 | |||||||
| chr11:43883525 | T | C | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.183+337T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883525 | |||||||
| chr11:43883546 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.183+358T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883546 | |||||||
| chr11:43883690 | A | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.184-293A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883690 | |||||||
| chr11:43883890 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.184-93C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883890 | |||||||
| chr11:43883934 | T | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.184-49T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883934 | |||||||
| chr11:43883967 | G | T | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.184-16G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 3/9 | chr11 | 43883967 | |||||||
| chr11:43884057 | T | TG | 1 | a0001c0002t0007g0026 | 3 | HG03139.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.218+41dupG | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884057 | ||||||
| chr11:43884305 | C | T | 2 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.218+288C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884305 | |||||||
| chr11:43884374 | T | C | 1 | a0002c0003t0002g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.218+357T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884374 | |||||||
| chr11:43884375 | CT | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(92): Show |
168 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.218+378delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | ||||||
| chr11:43884375 | CTT | C | 19 | a0001c0001t0001g0034 a0001c0001t0001g0110 a0001c0001t0001g0148 others(16): Show |
34 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.218+377_218+378del others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | ||||||
| chr11:43884375 | CTTT | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0225 a0001c0002t0007g0026 others(2): Show |
7 | HG00323.hp2 HG01261.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+376_218+378del others(3): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | ||||||
| chr11:43884375 | CTTTT | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
83 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.218+375_218+378del others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr11 | 43884375 | ||||||
| chr11:43884437 | T | A | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.218+420T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884437 | |||||||
| chr11:43884892 | C | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.218+875C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884892 | |||||||
| chr11:43884975 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.218+958C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884975 | |||||||
| chr11:43884985 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(89): Show |
150 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.218+968G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43884985 | |||||||
| chr11:43885146 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.218+1129T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885146 | |||||||
| chr11:43885150 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.218+1133A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885150 | |||||||
| chr11:43885272 | C | T | 16 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 others(13): Show |
32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.218+1255C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885272 | |||||||
| chr11:43885398 | T | C | 2 | a0002c0003t0002g0168 a0002c0003t0002g0169 |
2 | HG02630.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.219-1208T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885398 | |||||||
| chr11:43885524 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.219-1082G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885524 | |||||||
| chr11:43885538 | G | C | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-1068G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885538 | |||||||
| chr11:43885637 | C | G | 1 | a0001c0002t0001g0164 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.219-969C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885637 | |||||||
| chr11:43885778 | A | G | 5 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0188 others(2): Show |
7 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-828A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885778 | |||||||
| chr11:43885936 | A | G | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.219-670A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885936 | |||||||
| chr11:43885949 | A | G | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-657A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43885949 | |||||||
| chr11:43886011 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.219-595A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886011 | |||||||
| chr11:43886035 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.219-571G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886035 | |||||||
| chr11:43886062 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.219-544C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886062 | |||||||
| chr11:43886129 | A | G | 3 | a0001c0002t0004g0056 a0001c0002t0004g0211 a0001c0002t0004g0212 |
4 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-477A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886129 | |||||||
| chr11:43886243 | C | T | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.219-363C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886243 | |||||||
| chr11:43886365 | A | C | 1 | a0001c0001t0001g0133 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.219-241A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886365 | |||||||
| chr11:43886406 | C | A | 2 | a0001c0001t0001g0170 a0005c0008t0001g0171 |
2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.219-200C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886406 | |||||||
| chr11:43886554 | T | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.219-52T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 4/9 | chr11 | 43886554 | |||||||
| chr11:43886680 | C | T | 23 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0053 others(20): Show |
40 | HG00140.hp2 HG00741.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.266+27C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43886680 | |||||||
| chr11:43886916 | A | G | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.266+263A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43886916 | |||||||
| chr11:43886965 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.266+312T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43886965 | |||||||
| chr11:43887082 | GCATATGT others(4): Show |
G | 1 | a0002c0003t0002g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.266+432_266+442del others(11): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887082 | ||||||
| chr11:43887087 | T | C | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.266+434T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887087 | |||||||
| chr11:43887122 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.266+469C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887122 | |||||||
| chr11:43887164 | G | A | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+511G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887164 | |||||||
| chr11:43887212 | A | G | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.266+559A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887212 | |||||||
| chr11:43887286 | G | C | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+633G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887286 | |||||||
| chr11:43887535 | C | T | 1 | a0002c0003t0002g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.266+882C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887535 | |||||||
| chr11:43887544 | A | G | 1 | a0001c0002t0004g0224 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.266+891A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887544 | |||||||
| chr11:43887698 | A | G | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.266+1045A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887698 | |||||||
| chr11:43887703 | A | G | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.266+1050A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887703 | |||||||
| chr11:43887785 | G | GT | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.266+1141dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887785 | ||||||
| chr11:43887813 | G | C | 2 | a0002c0003t0002g0047 a0002c0003t0002g0172 |
3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.266+1160G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887813 | |||||||
| chr11:43887914 | G | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0145 |
2 | HG02165.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.266+1261G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887914 | |||||||
| chr11:43887936 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0001g0112 |
4 | HG01255.hp2 HG01258.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.266+1283G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887936 | |||||||
| chr11:43887955 | A | AT | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(23): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.266+1317dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887955 | ||||||
| chr11:43887955 | AT | A | 3 | a0001c0001t0001g0036 a0001c0002t0002g0003 a0001c0002t0002g0016 |
16 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.266+1317delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43887955 | ||||||
| chr11:43887964 | T | A | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.266+1311T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887964 | |||||||
| chr11:43887971 | G | T | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.266+1318G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887971 | |||||||
| chr11:43887999 | G | A | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.266+1346G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43887999 | |||||||
| chr11:43888043 | TGCCTTGG others(299): Show |
T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.266+1424_267-1343d others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr11 | 43888043 | ||||||
| chr11:43888382 | C | T | 35 | a0002c0003t0002g0007 a0002c0003t0002g0017 a0002c0003t0002g0018 others(32): Show |
50 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.267-1343C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888382 | |||||||
| chr11:43888537 | A | G | 3 | a0001c0002t0001g0055 a0001c0002t0001g0209 a0001c0002t0001g0210 |
4 | HG01243.hp1 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.267-1188A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888537 | |||||||
| chr11:43888693 | C | T | 1 | a0001c0002t0001g0163 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.267-1032C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888693 | |||||||
| chr11:43888807 | G | A | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.267-918G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888807 | |||||||
| chr11:43888875 | A | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.267-850A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43888875 | |||||||
| chr11:43889085 | A | G | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.267-640A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889085 | |||||||
| chr11:43889092 | C | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.267-633C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889092 | |||||||
| chr11:43889111 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0130 |
3 | HG00597.hp1 NA19005.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.267-614C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889111 | |||||||
| chr11:43889115 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.267-610A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889115 | |||||||
| chr11:43889188 | C | G | 1 | a0002c0003t0002g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.267-537C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889188 | |||||||
| chr11:43889211 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.267-514G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889211 | |||||||
| chr11:43889213 | C | T | 2 | a0001c0002t0001g0146 a0001c0002t0001g0147 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.267-512C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889213 | |||||||
| chr11:43889223 | C | T | 1 | a0001c0002t0001g0163 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.267-502C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889223 | |||||||
| chr11:43889261 | G | A | 2 | a0001c0002t0006g0188 a0001c0002t0006g0189 |
2 | HG02109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.267-464G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889261 | |||||||
| chr11:43889581 | G | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.267-144G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889581 | |||||||
| chr11:43889661 | A | G | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.267-64A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889661 | |||||||
| chr11:43889706 | A | G | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.267-19A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 5/9 | chr11 | 43889706 | |||||||
| chr11:43889918 | A | T | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.370+90A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43889918 | |||||||
| chr11:43890137 | C | CTA | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.370+310_370+311ins others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 43890137 | ||||||
| chr11:43890218 | C | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.370+390C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890218 | |||||||
| chr11:43890365 | C | T | 1 | a0001c0002t0004g0208 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.370+537C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890365 | |||||||
| chr11:43890366 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.370+538G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890366 | |||||||
| chr11:43890418 | C | T | 1 | a0001c0002t0006g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.370+590C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890418 | |||||||
| chr11:43890587 | T | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.370+759T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890587 | |||||||
| chr11:43890632 | G | A | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.370+804G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890632 | |||||||
| chr11:43890812 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.370+984C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890812 | |||||||
| chr11:43890819 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.370+991G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890819 | |||||||
| chr11:43890820 | C | T | 3 | a0002c0003t0002g0167 a0002c0003t0002g0181 a0002c0003t0002g0182 |
3 | HG01515.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.370+992C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890820 | |||||||
| chr11:43890982 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.371-1059A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43890982 | |||||||
| chr11:43891117 | C | T | 11 | a0001c0001t0005g0043 a0001c0001t0005g0044 a0001c0001t0005g0053 others(8): Show |
14 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.371-924C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891117 | |||||||
| chr11:43891241 | T | C | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.371-800T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891241 | |||||||
| chr11:43891326 | AAAATT | A | 4 | a0001c0001t0005g0053 a0001c0001t0005g0192 a0001c0001t0005g0193 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-707_371-703del others(5): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr11 | 43891326 | ||||||
| chr11:43891375 | C | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.371-666C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891375 | |||||||
| chr11:43891504 | T | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.371-537T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891504 | |||||||
| chr11:43891581 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.371-460C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891581 | |||||||
| chr11:43891687 | CAG | C | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.371-353_371-352del others(2): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891687 | |||||||
| chr11:43891836 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.371-205T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891836 | |||||||
| chr11:43891912 | T | C | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.371-129T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891912 | |||||||
| chr11:43891930 | T | C | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.371-111T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891930 | |||||||
| chr11:43891970 | A | G | 1 | a0001c0004t0003g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.371-71A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 6/9 | chr11 | 43891970 | |||||||
| chr11:43892157 | G | A | 16 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 others(13): Show |
32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.459+28G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892157 | |||||||
| chr11:43892406 | G | T | 5 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0188 others(2): Show |
7 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+277G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892406 | |||||||
| chr11:43892478 | A | G | 8 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG00673.hp1 HG02129.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+349A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892478 | |||||||
| chr11:43892483 | C | A | 6 | a0002c0003t0002g0017 a0002c0003t0002g0048 a0002c0003t0002g0166 others(3): Show |
10 | HG00642.hp2 HG00741.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.459+354C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892483 | |||||||
| chr11:43892651 | T | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.459+522T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892651 | |||||||
| chr11:43892663 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.459+534A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892663 | |||||||
| chr11:43892863 | GC | G | 35 | a0002c0003t0002g0007 a0002c0003t0002g0017 a0002c0003t0002g0018 others(32): Show |
50 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.459+735delC | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892863 | |||||||
| chr11:43892940 | A | G | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+811A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892940 | |||||||
| chr11:43892966 | A | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0069 a0001c0001t0001g0096 |
6 | HG00280.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+837A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892966 | |||||||
| chr11:43892988 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.459+859C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43892988 | |||||||
| chr11:43893002 | T | G | 1 | a0002c0003t0002g0048 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.459+873T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893002 | |||||||
| chr11:43893008 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.459+879G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893008 | |||||||
| chr11:43893022 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.459+893G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893022 | |||||||
| chr11:43893262 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.459+1133T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893262 | |||||||
| chr11:43893327 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.459+1198A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893327 | |||||||
| chr11:43893402 | C | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+1273C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893402 | |||||||
| chr11:43893463 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.459+1334C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893463 | |||||||
| chr11:43893786 | G | A | 3 | a0002c0003t0002g0033 a0002c0003t0002g0102 a0004c0010t0002g0033 |
3 | NA18961.hp1 NA18995.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.459+1657G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43893786 | |||||||
| chr11:43894017 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+1888T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894017 | |||||||
| chr11:43894320 | T | C | 1 | a0001c0002t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.459+2191T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894320 | |||||||
| chr11:43894703 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.459+2574G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894703 | |||||||
| chr11:43894715 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.459+2586C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894715 | |||||||
| chr11:43894800 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.459+2671C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894800 | |||||||
| chr11:43894832 | T | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.459+2703T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43894832 | |||||||
| chr11:43895006 | C | G | 1 | a0001c0001t0001g0041 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.459+2877C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895006 | |||||||
| chr11:43895267 | G | A | 8 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG00673.hp1 HG02129.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+3138G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895267 | |||||||
| chr11:43895308 | G | A | 1 | a0001c0004t0003g0027 | 2 | HG00609.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.459+3179G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895308 | |||||||
| chr11:43895360 | C | A | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.459+3231C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895360 | |||||||
| chr11:43895491 | A | G | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+3362A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895491 | |||||||
| chr11:43895692 | C | T | 2 | a0001c0001t0005g0053 a0001c0001t0005g0193 |
3 | HG00741.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.459+3563C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43895692 | |||||||
| chr11:43896021 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.459+3892C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896021 | |||||||
| chr11:43896037 | T | C | 1 | a0002c0003t0002g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.459+3908T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896037 | |||||||
| chr11:43896068 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.459+3939G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896068 | |||||||
| chr11:43896102 | C | T | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+3973C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896102 | |||||||
| chr11:43896159 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.459+4030T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896159 | |||||||
| chr11:43896217 | G | A | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+4088G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896217 | |||||||
| chr11:43896268 | T | TAC | 28 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0111 others(25): Show |
45 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.459+4170_459+4171d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | ||||||
| chr11:43896268 | T | TACAC | 10 | a0001c0002t0001g0055 a0001c0002t0006g0052 a0001c0002t0006g0187 others(7): Show |
14 | HG02145.hp2 HG02572.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.459+4168_459+4171d others(6): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | ||||||
| chr11:43896268 | T | TACACAC | 3 | a0001c0001t0001g0110 a0001c0002t0006g0051 a0001c0002t0006g0188 |
4 | HG00140.hp2 HG02109.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+4166_459+4171d others(8): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | ||||||
| chr11:43896268 | TAC | T | 11 | a0001c0001t0001g0129 a0001c0001t0001g0141 a0001c0001t0001g0142 others(8): Show |
11 | HG00673.hp1 HG00741.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.459+4170_459+4171d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | ||||||
| chr11:43896268 | TACAC | T | 35 | a0001c0001t0001g0021 a0001c0001t0001g0125 a0001c0001t0001g0126 others(32): Show |
52 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.459+4168_459+4171d others(6): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | ||||||
| chr11:43896268 | TACACACA others(3): Show |
T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0148 a0001c0001t0005g0158 |
3 | HG02280.hp2 HG03486.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.459+4162_459+4171d others(12): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | ||||||
| chr11:43896268 | TACACACA others(5): Show |
T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.459+4160_459+4171d others(14): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43896268 | ||||||
| chr11:43896426 | C | T | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+4297C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896426 | |||||||
| chr11:43896603 | C | A | 1 | a0001c0001t0005g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+4474C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896603 | |||||||
| chr11:43896726 | A | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4597A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896726 | |||||||
| chr11:43896735 | T | C | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4606T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896735 | |||||||
| chr11:43896736 | G | A | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4607G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896736 | |||||||
| chr11:43896737 | C | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+4608C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896737 | |||||||
| chr11:43896737 | CT | C | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.459+4609delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896737 | |||||||
| chr11:43896828 | G | A | 1 | a0002c0003t0002g0174 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.460-4688G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896828 | |||||||
| chr11:43896856 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.460-4660T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896856 | |||||||
| chr11:43896990 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.460-4526T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43896990 | |||||||
| chr11:43897256 | G | A | 2 | a0001c0002t0004g0058 a0001c0002t0004g0222 |
3 | HG01256.hp2 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.460-4260G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897256 | |||||||
| chr11:43897279 | C | T | 1 | a0001c0002t0006g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.460-4237C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897279 | |||||||
| chr11:43897542 | G | C | 4 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(1): Show |
4 | HG01243.hp2 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3974G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897542 | |||||||
| chr11:43897594 | A | G | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-3922A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897594 | |||||||
| chr11:43897686 | C | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG02132.hp1 HG02135.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.460-3830C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897686 | |||||||
| chr11:43897703 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.460-3813A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897703 | |||||||
| chr11:43897707 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
6 | NA18944.hp1 NA18947.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-3809C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897707 | |||||||
| chr11:43897836 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.460-3680A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897836 | |||||||
| chr11:43897861 | A | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.460-3655A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43897861 | |||||||
| chr11:43898068 | CAAG | C | 16 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 others(13): Show |
32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.460-3447_460-3445d others(5): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898068 | |||||||
| chr11:43898112 | C | G | 2 | a0002c0003t0002g0047 a0002c0003t0002g0172 |
3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.460-3404C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898112 | |||||||
| chr11:43898144 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(113): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.460-3372C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898144 | |||||||
| chr11:43898228 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(113): Show |
191 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.460-3288C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898228 | |||||||
| chr11:43898236 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(121): Show |
201 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.460-3280C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898236 | |||||||
| chr11:43898365 | C | T | 2 | a0002c0003t0002g0047 a0002c0003t0002g0172 |
3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.460-3151C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898365 | |||||||
| chr11:43898431 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.460-3085C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898431 | |||||||
| chr11:43898456 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.460-3060A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898456 | |||||||
| chr11:43898488 | C | T | 1 | a0001c0002t0001g0057 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.460-3028C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898488 | |||||||
| chr11:43898503 | C | T | 3 | a0001c0004t0003g0028 a0001c0004t0003g0029 a0001c0004t0003g0066 |
5 | HG00639.hp1 HG01081.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-3013C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898503 | |||||||
| chr11:43898559 | G | A | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-2957G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898559 | |||||||
| chr11:43898766 | C | T | 1 | a0001c0001t0005g0053 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.460-2750C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43898766 | |||||||
| chr11:43899119 | A | G | 1 | a0001c0002t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.460-2397A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899119 | |||||||
| chr11:43899173 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.460-2343C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899173 | |||||||
| chr11:43899295 | C | T | 1 | a0002c0003t0002g0106 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.460-2221C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899295 | |||||||
| chr11:43899403 | C | T | 1 | a0001c0002t0001g0204 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.460-2113C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899403 | |||||||
| chr11:43899429 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.460-2087G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899429 | |||||||
| chr11:43899447 | G | A | 16 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 others(13): Show |
32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.460-2069G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899447 | |||||||
| chr11:43899504 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.460-2012T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899504 | |||||||
| chr11:43899605 | C | T | 3 | a0001c0002t0006g0051 a0001c0002t0006g0188 a0001c0002t0006g0189 |
4 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-1911C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899605 | |||||||
| chr11:43899647 | A | T | 2 | a0001c0001t0005g0156 a0001c0001t0005g0157 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.460-1869A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899647 | |||||||
| chr11:43899816 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-1700G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899816 | |||||||
| chr11:43899861 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0002t0001g0203 others(8): Show |
11 | HG00140.hp1 HG01361.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-1655C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43899861 | |||||||
| chr11:43899872 | G | GA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(69): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.460-1627dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43899872 | ||||||
| chr11:43899872 | G | GAA | 22 | a0001c0001t0001g0114 a0001c0001t0001g0205 a0001c0001t0005g0043 others(19): Show |
38 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.460-1628_460-1627d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43899872 | ||||||
| chr11:43900083 | A | AAG | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(188): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.460-1432_460-1431i others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900083 | ||||||
| chr11:43900087 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.460-1429T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900087 | |||||||
| chr11:43900215 | A | AATT | 19 | a0001c0001t0001g0032 a0001c0001t0001g0071 a0001c0001t0001g0074 others(16): Show |
33 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.460-1301_460-1300i others(5): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900215 | |||||||
| chr11:43900215 | A | AATTT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(33): Show |
66 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.460-1301_460-1300i others(6): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900215 | |||||||
| chr11:43900215 | A | AATTTT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0031 others(8): Show |
19 | HG00735.hp2 HG01175.hp2 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.460-1301_460-1300i others(7): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900215 | |||||||
| chr11:43900215 | A | AT | 11 | a0001c0002t0001g0046 a0001c0002t0001g0055 a0001c0002t0001g0199 others(8): Show |
18 | HG01109.hp1 HG01109.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.460-1275dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900215 | ||||||
| chr11:43900215 | AT | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0020 others(75): Show |
131 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.460-1275delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900215 | ||||||
| chr11:43900215 | ATT | A | 5 | a0002c0003t0002g0048 a0002c0003t0002g0167 a0002c0003t0002g0174 others(2): Show |
6 | HG01070.hp2 HG01081.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-1276_460-1275d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr11 | 43900215 | ||||||
| chr11:43900219 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.460-1297T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900219 | |||||||
| chr11:43900244 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(91): Show |
152 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.460-1272G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900244 | |||||||
| chr11:43900249 | A | G | 16 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 others(13): Show |
32 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.460-1267A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900249 | |||||||
| chr11:43900368 | C | T | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-1148C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900368 | |||||||
| chr11:43900415 | G | A | 1 | a0001c0002t0004g0211 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.460-1101G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900415 | |||||||
| chr11:43900455 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.460-1061C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900455 | |||||||
| chr11:43900469 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.460-1047G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900469 | |||||||
| chr11:43900474 | G | T | 1 | a0005c0008t0001g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.460-1042G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900474 | |||||||
| chr11:43900517 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.460-999T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43900517 | |||||||
| chr11:43901186 | G | A | 1 | a0001c0002t0006g0190 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.460-330G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43901186 | |||||||
| chr11:43901226 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.460-290G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43901226 | |||||||
| chr11:43901378 | G | A | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.460-138G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 7/9 | chr11 | 43901378 | |||||||
| chr11:43901761 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.669+36C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43901761 | |||||||
| chr11:43901913 | A | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(188): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.669+188A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43901913 | |||||||
| chr11:43901994 | A | G | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+269A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43901994 | |||||||
| chr11:43902024 | T | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(188): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.669+299T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902024 | |||||||
| chr11:43902055 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.669+330G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902055 | |||||||
| chr11:43902565 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.669+840G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902565 | |||||||
| chr11:43902627 | A | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+902A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902627 | |||||||
| chr11:43902710 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.669+985C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902710 | |||||||
| chr11:43902721 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.669+996C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902721 | |||||||
| chr11:43902779 | G | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(189): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.669+1054G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902779 | |||||||
| chr11:43902899 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.669+1174G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902899 | |||||||
| chr11:43902927 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.669+1202A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902927 | |||||||
| chr11:43902960 | C | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+1235C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43902960 | |||||||
| chr11:43903011 | G | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
43 | HG00423.hp1 HG00735.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.669+1286G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903011 | |||||||
| chr11:43903080 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(41): Show |
75 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.669+1355T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903080 | |||||||
| chr11:43903156 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.669+1431G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903156 | |||||||
| chr11:43903172 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.669+1447G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903172 | |||||||
| chr11:43903196 | C | T | 1 | a0001c0002t0006g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.669+1471C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903196 | |||||||
| chr11:43903197 | T | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(49): Show |
85 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.669+1472T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903197 | |||||||
| chr11:43903245 | G | A | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+1520G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903245 | |||||||
| chr11:43903259 | T | C | 1 | a0001c0002t0007g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.669+1534T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903259 | |||||||
| chr11:43903338 | A | G | 1 | a0001c0002t0001g0159 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.669+1613A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903338 | |||||||
| chr11:43903378 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(46): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.669+1653C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903378 | |||||||
| chr11:43903466 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.669+1741A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903466 | |||||||
| chr11:43903516 | G | A | 17 | a0001c0001t0001g0032 a0001c0002t0007g0026 a0001c0002t0007g0215 others(14): Show |
34 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.669+1791G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903516 | |||||||
| chr11:43903519 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.669+1794A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903519 | |||||||
| chr11:43903528 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.669+1803T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903528 | |||||||
| chr11:43903529 | G | A | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(40): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.669+1804G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903529 | |||||||
| chr11:43903602 | C | T | 3 | a0002c0003t0002g0167 a0002c0003t0002g0181 a0002c0003t0002g0182 |
3 | HG01515.hp2 HG04228.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.669+1877C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903602 | |||||||
| chr11:43903612 | A | G | 1 | a0001c0002t0001g0161 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.669+1887A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903612 | |||||||
| chr11:43903703 | G | C | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.669+1978G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903703 | |||||||
| chr11:43903884 | G | A | 2 | a0001c0002t0001g0206 a0001c0002t0001g0207 |
2 | HG01891.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.669+2159G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903884 | |||||||
| chr11:43903890 | T | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.669+2165T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903890 | |||||||
| chr11:43903988 | A | T | 3 | a0001c0002t0001g0055 a0001c0002t0001g0209 a0001c0002t0001g0210 |
4 | HG01243.hp1 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+2263A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43903988 | |||||||
| chr11:43904379 | C | T | 1 | a0001c0004t0003g0065 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.669+2654C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904379 | |||||||
| chr11:43904674 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.669+2949A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904674 | |||||||
| chr11:43904772 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.669+3047G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904772 | |||||||
| chr11:43904800 | C | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.669+3075C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43904800 | |||||||
| chr11:43905099 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.669+3374A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905099 | |||||||
| chr11:43905118 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.669+3393G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905118 | |||||||
| chr11:43905127 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.669+3402C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905127 | |||||||
| chr11:43905192 | T | TG | 3 | a0001c0001t0001g0040 a0001c0001t0001g0132 a0001c0001t0001g0145 |
4 | HG00408.hp2 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+3468dupG | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43905192 | ||||||
| chr11:43905396 | C | T | 2 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.669+3671C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905396 | |||||||
| chr11:43905442 | G | GT | 16 | a0001c0001t0001g0068 a0001c0002t0004g0058 a0001c0004t0003g0004 others(13): Show |
31 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.669+3728dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43905442 | ||||||
| chr11:43905465 | G | T | 6 | a0001c0002t0001g0008 a0001c0002t0001g0057 a0001c0002t0001g0194 others(3): Show |
12 | HG00544.hp1 HG00673.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+3740G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905465 | |||||||
| chr11:43905527 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0124 a0001c0001t0001g0132 others(1): Show |
5 | HG00408.hp2 HG02165.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+3802A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905527 | |||||||
| chr11:43905658 | T | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.669+3933T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905658 | |||||||
| chr11:43905714 | G | A | 2 | a0002c0003t0002g0047 a0002c0003t0002g0172 |
3 | HG02258.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.669+3989G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905714 | |||||||
| chr11:43905740 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(189): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.669+4015A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905740 | |||||||
| chr11:43905846 | T | C | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+4121T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43905846 | |||||||
| chr11:43906046 | C | A | 1 | a0001c0002t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.669+4321C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906046 | |||||||
| chr11:43906123 | T | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
200 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.669+4398T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906123 | |||||||
| chr11:43906138 | T | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(64): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.669+4413T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906138 | |||||||
| chr11:43906229 | C | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.669+4504C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906229 | |||||||
| chr11:43906237 | T | C | 6 | a0001c0001t0005g0053 a0001c0001t0005g0192 a0001c0001t0005g0193 others(3): Show |
7 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+4512T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906237 | |||||||
| chr11:43906306 | A | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.669+4581A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906306 | |||||||
| chr11:43906745 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.669+5020A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906745 | |||||||
| chr11:43906747 | C | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.669+5022C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906747 | |||||||
| chr11:43906973 | T | G | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+5248T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43906973 | |||||||
| chr11:43907115 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.669+5390T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907115 | |||||||
| chr11:43907212 | A | AGT | 16 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0198 others(13): Show |
29 | HG00423.hp2 HG00609.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.669+5503_669+5504d others(4): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43907212 | ||||||
| chr11:43907228 | T | C | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+5503T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907228 | |||||||
| chr11:43907249 | A | T | 1 | a0001c0001t0001g0083 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.669+5524A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907249 | |||||||
| chr11:43907308 | G | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.669+5583G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907308 | |||||||
| chr11:43907317 | C | G | 2 | a0001c0002t0004g0056 a0001c0002t0004g0211 |
3 | HG02451.hp1 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.669+5592C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907317 | |||||||
| chr11:43907400 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.669+5675C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907400 | |||||||
| chr11:43907667 | G | A | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.669+5942G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907667 | |||||||
| chr11:43907899 | T | C | 1 | a0001c0004t0003g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.669+6174T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907899 | |||||||
| chr11:43907942 | G | A | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+6217G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907942 | |||||||
| chr11:43907949 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.669+6224A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43907949 | |||||||
| chr11:43908342 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.669+6617G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908342 | |||||||
| chr11:43908451 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0084 |
2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.669+6726G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908451 | |||||||
| chr11:43908458 | G | A | 1 | a0001c0002t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.669+6733G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908458 | |||||||
| chr11:43908461 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.669+6736A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908461 | |||||||
| chr11:43908692 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.669+6967C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908692 | |||||||
| chr11:43908694 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.669+6969G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908694 | |||||||
| chr11:43908709 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.669+6984C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908709 | |||||||
| chr11:43908754 | C | T | 11 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0113 others(8): Show |
13 | HG00280.hp1 HG00323.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.669+7029C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908754 | |||||||
| chr11:43908764 | A | G | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+7039A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908764 | |||||||
| chr11:43908891 | G | A | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.669+7166G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43908891 | |||||||
| chr11:43909133 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0085 |
5 | HG00423.hp1 HG01943.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+7408G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909133 | |||||||
| chr11:43909498 | G | A | 1 | a0002c0003t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.669+7773G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909498 | |||||||
| chr11:43909511 | A | C | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.669+7786A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909511 | |||||||
| chr11:43909876 | C | G | 3 | a0001c0002t0006g0051 a0001c0002t0006g0188 a0001c0002t0006g0189 |
4 | HG00140.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+8151C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43909876 | |||||||
| chr11:43910063 | G | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.669+8338G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910063 | |||||||
| chr11:43910287 | CT | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(20): Show |
44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.669+8563delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910287 | |||||||
| chr11:43910336 | T | A | 2 | a0001c0002t0006g0052 a0001c0002t0006g0190 |
3 | HG02970.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.669+8611T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910336 | |||||||
| chr11:43910451 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.670-8587G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910451 | |||||||
| chr11:43910562 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.670-8476A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910562 | |||||||
| chr11:43910624 | C | T | 1 | a0001c0004t0003g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.670-8414C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910624 | |||||||
| chr11:43910786 | C | CT | 33 | a0001c0001t0001g0170 a0001c0001t0005g0043 a0001c0001t0005g0044 others(30): Show |
62 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.670-8243dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43910786 | ||||||
| chr11:43910795 | T | C | 3 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0199 |
3 | HG01243.hp2 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.670-8243T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910795 | |||||||
| chr11:43910948 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0100 |
2 | HG01516.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.670-8090G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43910948 | |||||||
| chr11:43911135 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.670-7903A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911135 | |||||||
| chr11:43911290 | G | A | 13 | a0001c0004t0003g0004 a0001c0004t0003g0009 a0001c0004t0003g0027 others(10): Show |
27 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.670-7748G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911290 | |||||||
| chr11:43911309 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0072 a0001c0001t0001g0074 others(6): Show |
11 | HG00735.hp2 HG01175.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.670-7729G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911309 | |||||||
| chr11:43911443 | A | C | 3 | a0001c0001t0001g0205 a0001c0002t0001g0054 a0001c0002t0001g0202 |
4 | HG01109.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-7595A>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911443 | |||||||
| chr11:43911757 | C | T | 4 | a0001c0002t0001g0008 a0001c0002t0001g0194 a0001c0002t0001g0200 others(1): Show |
9 | HG00544.hp1 HG00673.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.670-7281C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911757 | |||||||
| chr11:43911849 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.670-7189G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911849 | |||||||
| chr11:43911888 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(194): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.670-7150T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911888 | |||||||
| chr11:43911919 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.670-7119G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911919 | |||||||
| chr11:43911950 | G | A | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-7088G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911950 | |||||||
| chr11:43911983 | C | T | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-7055C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911983 | |||||||
| chr11:43911994 | G | A | 2 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-7044G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43911994 | |||||||
| chr11:43912078 | G | A | 1 | a0005c0008t0001g0171 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.670-6960G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912078 | |||||||
| chr11:43912089 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0082 |
2 | NA19001.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.670-6949C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912089 | |||||||
| chr11:43912139 | C | CA | 38 | a0002c0003t0002g0007 a0002c0003t0002g0017 a0002c0003t0002g0018 others(35): Show |
53 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.670-6893dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43912139 | ||||||
| chr11:43912268 | T | C | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-6770T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912268 | |||||||
| chr11:43912324 | C | T | 1 | a0002c0003t0002g0182 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.670-6714C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912324 | |||||||
| chr11:43912412 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
97 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.670-6626C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912412 | |||||||
| chr11:43912571 | G | A | 53 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(50): Show |
74 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.670-6467G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912571 | |||||||
| chr11:43912921 | T | C | 53 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(50): Show |
74 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.670-6117T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43912921 | |||||||
| chr11:43912992 | TAAGTCAA others(12): Show |
T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.670-6026_670-6008d others(21): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43912992 | ||||||
| chr11:43913042 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(82): Show |
145 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.670-5996C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913042 | |||||||
| chr11:43913106 | T | TA | 15 | a0001c0001t0001g0078 a0001c0002t0001g0045 a0001c0002t0001g0046 others(12): Show |
31 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.670-5916dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43913106 | ||||||
| chr11:43913133 | C | T | 1 | a0001c0002t0001g0213 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.670-5905C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913133 | |||||||
| chr11:43913151 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.670-5887T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913151 | |||||||
| chr11:43913167 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.670-5871A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913167 | |||||||
| chr11:43913194 | T | G | 1 | a0001c0002t0002g0152 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-5844T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913194 | |||||||
| chr11:43913244 | A | T | 1 | a0001c0001t0001g0100 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.670-5794A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913244 | |||||||
| chr11:43913297 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.670-5741C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913297 | |||||||
| chr11:43913554 | G | T | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-5484G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913554 | |||||||
| chr11:43913557 | C | T | 8 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(5): Show |
10 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-5481C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913557 | |||||||
| chr11:43913573 | C | T | 3 | a0002c0003t0002g0033 a0002c0003t0002g0102 a0004c0010t0002g0033 |
3 | NA18961.hp1 NA18995.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.670-5465C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913573 | |||||||
| chr11:43913615 | T | C | 5 | a0002c0003t0002g0049 a0002c0003t0002g0179 a0002c0003t0002g0184 others(2): Show |
6 | HG01074.hp2 HG01175.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-5423T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913615 | |||||||
| chr11:43913796 | T | A | 1 | a0003c0005t0001g0030 | 2 | NA18947.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.670-5242T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43913796 | |||||||
| chr11:43914139 | G | T | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-4899G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914139 | |||||||
| chr11:43914412 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.670-4626G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914412 | |||||||
| chr11:43914434 | G | A | 53 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(50): Show |
74 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.670-4604G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914434 | |||||||
| chr11:43914447 | G | C | 1 | a0001c0001t0001g0035 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.670-4591G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914447 | |||||||
| chr11:43914529 | G | A | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-4509G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914529 | |||||||
| chr11:43914566 | T | TA | 42 | a0001c0001t0001g0225 a0001c0002t0002g0003 a0001c0002t0002g0016 others(39): Show |
69 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.670-4462dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43914566 | ||||||
| chr11:43914566 | TA | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.670-4462delA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43914566 | ||||||
| chr11:43914589 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(192): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.670-4449A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914589 | |||||||
| chr11:43914653 | C | T | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-4385C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43914653 | |||||||
| chr11:43915123 | G | A | 1 | a0001c0002t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.670-3915G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915123 | |||||||
| chr11:43915124 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0009g0014 |
5 | HG00639.hp2 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-3914C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915124 | |||||||
| chr11:43915215 | G | GA | 7 | a0001c0001t0001g0072 a0001c0001t0001g0121 a0001c0001t0005g0158 others(4): Show |
7 | HG01981.hp1 HG02738.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-3807dupA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43915215 | ||||||
| chr11:43915215 | GA | G | 10 | a0001c0001t0001g0077 a0001c0002t0001g0008 a0001c0002t0001g0057 others(7): Show |
16 | HG00544.hp1 HG00673.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.670-3807delA | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43915215 | ||||||
| chr11:43915247 | T | A | 1 | a0001c0001t0005g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.670-3791T>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915247 | |||||||
| chr11:43915275 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.670-3763T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915275 | |||||||
| chr11:43915395 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(88): Show |
163 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.670-3643T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915395 | |||||||
| chr11:43915430 | C | G | 8 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0159 others(5): Show |
10 | HG01928.hp1 HG02293.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-3608C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915430 | |||||||
| chr11:43915493 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.670-3545C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915493 | |||||||
| chr11:43915539 | A | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(85): Show |
148 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.670-3499A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915539 | |||||||
| chr11:43915540 | A | T | 1 | a0001c0002t0001g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.670-3498A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915540 | |||||||
| chr11:43915567 | A | G | 1 | a0001c0002t0001g0160 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.670-3471A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915567 | |||||||
| chr11:43915589 | C | T | 1 | a0001c0002t0001g0199 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.670-3449C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915589 | |||||||
| chr11:43915662 | AG | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(133): Show |
232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.670-3374delG | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43915662 | ||||||
| chr11:43915866 | C | T | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-3172C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43915866 | |||||||
| chr11:43916037 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.670-3001T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916037 | |||||||
| chr11:43916169 | G | A | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-2869G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916169 | |||||||
| chr11:43916244 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.670-2794G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916244 | |||||||
| chr11:43916409 | C | A | 8 | a0001c0002t0004g0022 a0001c0002t0004g0024 a0001c0002t0004g0056 others(5): Show |
13 | HG02109.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-2629C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916409 | |||||||
| chr11:43916480 | G | A | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-2558G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916480 | |||||||
| chr11:43916526 | T | TTTATCCT others(23): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0078 others(3): Show |
9 | NA18978.hp1 NA18979.hp2 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.670-2509_670-2480d others(32): Show |
ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43916526 | ||||||
| chr11:43916764 | A | G | 1 | a0001c0004t0003g0062 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.670-2274A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916764 | |||||||
| chr11:43916809 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.670-2229G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916809 | |||||||
| chr11:43916889 | G | A | 6 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(3): Show |
8 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.670-2149G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43916889 | |||||||
| chr11:43917048 | G | C | 37 | a0002c0003t0002g0007 a0002c0003t0002g0017 a0002c0003t0002g0018 others(34): Show |
52 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.670-1990G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917048 | |||||||
| chr11:43917117 | G | A | 3 | a0001c0002t0007g0026 a0001c0002t0007g0215 a0001c0002t0007g0216 |
5 | HG02717.hp2 HG03139.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-1921G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917117 | |||||||
| chr11:43917226 | C | A | 1 | a0006c0011t0002g0149 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670-1812C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917226 | |||||||
| chr11:43917563 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.670-1475C>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917563 | |||||||
| chr11:43917645 | A | AT | 18 | a0001c0001t0001g0133 a0001c0002t0001g0045 a0001c0002t0001g0046 others(15): Show |
24 | HG00140.hp2 HG01928.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.670-1383dupT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43917645 | ||||||
| chr11:43917947 | T | G | 15 | a0001c0002t0001g0054 a0001c0002t0001g0196 a0001c0002t0001g0197 others(12): Show |
23 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.670-1091T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43917947 | |||||||
| chr11:43918030 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG02004.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.670-1008T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918030 | |||||||
| chr11:43918076 | C | T | 9 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(6): Show |
13 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-962C>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918076 | |||||||
| chr11:43918078 | G | A | 38 | a0002c0003t0002g0007 a0002c0003t0002g0017 a0002c0003t0002g0018 others(35): Show |
53 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.670-960G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918078 | |||||||
| chr11:43918214 | C | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(79): Show |
154 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.670-824C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918214 | |||||||
| chr11:43918230 | G | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
14 | HG00280.hp1 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-808G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918230 | |||||||
| chr11:43918372 | C | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(132): Show |
243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.670-666C>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918372 | |||||||
| chr11:43918434 | T | G | 2 | a0001c0002t0001g0046 a0001c0002t0001g0162 |
3 | NA18969.hp2 NA18985.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.670-604T>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918434 | |||||||
| chr11:43918704 | T | C | 9 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(6): Show |
13 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-334T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918704 | |||||||
| chr11:43918916 | T | C | 2 | a0001c0002t0001g0213 a0001c0002t0001g0214 |
2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.670-122T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43918916 | |||||||
| chr11:43918956 | AT | A | 9 | a0001c0002t0006g0051 a0001c0002t0006g0052 a0001c0002t0006g0187 others(6): Show |
13 | HG00140.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-73delT | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr11 | 43918956 | ||||||
| chr11:43919016 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(189): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.670-22T>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 8/9 | chr11 | 43919016 | |||||||
| chr11:43919212 | G | C | 1 | a0001c0002t0001g0200 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.768+76G>C | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919212 | |||||||
| chr11:43919215 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.768+79A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919215 | |||||||
| chr11:43919353 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.768+217G>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919353 | |||||||
| chr11:43919576 | A | G | 3 | a0001c0002t0002g0003 a0001c0002t0002g0016 a0001c0002t0002g0152 |
15 | HG01109.hp2 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.769-342A>G | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919576 | |||||||
| chr11:43919820 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.769-98G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919820 | |||||||
| chr11:43919825 | A | T | 1 | a0001c0001t0005g0158 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.769-93A>T | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919825 | |||||||
| chr11:43919873 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.769-45G>A | ALKBH3 | ENSG00000166199.13 | transcript | ENST00000302708.9 | protein_coding | 9/9 | chr11 | 43919873 |