Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 83592 |
|---|---|
| ensemblid | ENSG00000165568.18 |
| hgncid | 23437 |
| symbol | AKR1E2 |
| name | aldo-keto reductase family 1 member E2 |
| refseq_nuc | NM_001040177.3 |
| refseq_prot | NP_001035267.1 |
| ensembl_nuc | ENST00000298375.12 |
| ensembl_prot | ENSP00000298375.7 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 4826207 |
| end | 4848062 |
| strand | + |
| ver | v1.2 |
| region | chr10:4826207-4848062 |
| region5000 | chr10:4821207-4853062 |
| regionname0 | AKR1E2_chr10_4826207_4848062 |
| regionname5000 | AKR1E2_chr10_4821207_4853062 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 320 | 296 | 78 | 58 | 114 | 10 | 34 | 76 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0002 | 0/0 | 320 | 29 | 1 | 3 | 25 | 0 | 0 | 21 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0003 | 0/0 | 300 | 11 | 2 | 5 | 0 | 0 | 4 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0004 | 0/0 | 320 | 11 | 3 | 8 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0005 | 0/0 | 320 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0006 | 0/0 | 320 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0007 | 0/0 | 320 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0008 | 0/0 | 320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0009 | 0/0 | 320 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 963 | 294 | 77 | 57 | 114 | 10 | 34 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0002 | 0/0 | 963 | 29 | 1 | 3 | 25 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0003 | 0/0 | 963 | 11 | 3 | 8 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0004 | 0/0 | 963 | 11 | 2 | 5 | 0 | 0 | 4 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0005 | 0/0 | 963 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0006 | 0/0 | 963 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0007 | 0/0 | 963 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0008 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0009 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0010 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| c0011 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 651 | 230 | 32 | 50 | 112 | 10 | 25 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0002 | 1/0 | 651 | 61 | 42 | 6 | 2 | 0 | 10 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0003 | 0/0 | 652 | 27 | 1 | 3 | 23 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0004 | 0/0 | 651 | 13 | 4 | 9 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0005 | 0/0 | 651 | 8 | 2 | 3 | 0 | 0 | 3 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0006 | 0/0 | 643 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0007 | 0/0 | 651 | 3 | 0 | 2 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0008 | 0/0 | 651 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0009 | 0/0 | 651 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0010 | 0/0 | 659 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0011 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0012 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0013 | 0/0 | 651 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0014 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| t0015 | 0/0 | 651 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 52 | 1 | 18 | 27 | 0 | 6 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0002 | 0/0 | 39 | 1 | 9 | 20 | 2 | 7 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0003 | 0/0 | 16 | 11 | 0 | 0 | 0 | 5 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0004 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0005 | 0/0 | 10 | 2 | 3 | 3 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0006 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0012 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0017 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0019 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0021 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0023 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 963 | 294 | 77 | 57 | 114 | 10 | 34 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0009 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0011 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0002c0002 | 0/0 | 963 | 29 | 1 | 3 | 25 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0003c0004 | 0/0 | 963 | 11 | 2 | 5 | 0 | 0 | 4 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0004c0003 | 0/0 | 963 | 11 | 3 | 8 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0005c0005 | 0/0 | 963 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0006c0006 | 0/0 | 963 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0007c0007 | 0/0 | 963 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0008c0010 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0009c0008 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1613 | 224 | 32 | 49 | 109 | 10 | 23 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0002 | 1/0 | 1613 | 58 | 39 | 6 | 2 | 0 | 10 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0004 | 0/0 | 1613 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0008 | 0/0 | 1613 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0009 | 0/0 | 1613 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0010 | 0/0 | 1621 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0011 | 0/0 | 1613 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0013 | 0/0 | 1613 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0001t0015 | 0/0 | 1613 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0009t0002 | 0/0 | 1613 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0001c0011t0001 | 0/0 | 1613 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0002c0002t0003 | 0/0 | 1614 | 27 | 1 | 3 | 23 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0002c0002t0012 | 0/0 | 1622 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0002c0002t0014 | 0/0 | 1614 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0003c0004t0005 | 0/0 | 1613 | 8 | 2 | 3 | 0 | 0 | 3 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0003c0004t0007 | 0/0 | 1613 | 3 | 0 | 2 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0004c0003t0004 | 0/0 | 1613 | 11 | 3 | 8 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0005c0005t0006 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0006c0006t0001 | 0/0 | 1613 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0007c0007t0002 | 0/0 | 1613 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0008c0010t0001 | 0/0 | 1613 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| a0009c0008t0001 | 0/0 | 1613 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | copy fasta | chr10 | 4821207 | 4853062 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 50 | 1 | 17 | 26 | 0 | 6 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0002 | 0/0 | 34 | 1 | 6 | 20 | 2 | 5 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0004 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0005 | 0/0 | 10 | 2 | 3 | 3 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 6 | 0 | 2 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0007 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0012 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0017 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0003 | 0/0 | 16 | 11 | 0 | 0 | 0 | 5 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0019 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0004g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0009g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0010g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0011g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0001t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0009t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0001c0011t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0012g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0002c0002t0014g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0005g0023 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0005g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0005g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0005g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0007g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0007g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0003c0004t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0003t0004g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0003t0004g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0003t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0003t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0004c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0005c0005t0006g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0005c0005t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0006c0006t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0007c0007t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0008c0010t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| a0009c0008t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | GBR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00642 | hp2 | a0001 | c0011 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00735 | hp1 | a0004 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00741 | hp1 | a0004 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0024 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01070 | hp2 | a0004 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01071 | hp2 | a0004 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01074 | hp2 | a0004 | c0003 | t0004 | g0010 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0024 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01167 | hp2 | a0004 | c0003 | t0004 | g0020 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01169 | hp2 | a0004 | c0003 | t0004 | g0020 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01175 | hp2 | a0003 | c0004 | t0005 | g0147 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01346 | hp2 | a0003 | c0004 | t0005 | g0039 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01433 | hp2 | a0004 | c0003 | t0004 | g0020 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01928 | hp1 | a0003 | c0004 | t0005 | g0039 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01928 | hp2 | a0003 | c0004 | t0007 | g0145 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01952 | hp1 | a0001 | c0001 | t0015 | g0017 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01981 | hp2 | a0003 | c0004 | t0007 | g0023 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02015 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0052 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02155 | hp2 | a0002 | c0002 | t0012 | g0015 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02622 | hp1 | a0005 | c0005 | t0006 | g0022 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02717 | hp1 | a0007 | c0007 | t0002 | g0031 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02723 | hp2 | a0004 | c0003 | t0004 | g0043 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02735 | hp2 | a0009 | c0008 | t0001 | g0113 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02886 | hp1 | a0005 | c0005 | t0006 | g0022 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02922 | hp1 | a0007 | c0007 | t0002 | g0031 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03130 | hp1 | a0001 | c0009 | t0002 | g0021 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03195 | hp1 | a0005 | c0005 | t0006 | g0109 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0026 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03209 | hp1 | a0003 | c0004 | t0005 | g0045 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03239 | hp1 | a0003 | c0004 | t0007 | g0078 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0047 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0074 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03490 | hp2 | a0003 | c0004 | t0005 | g0144 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03492 | hp2 | a0003 | c0004 | t0005 | g0146 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03540 | hp2 | a0004 | c0003 | t0004 | g0042 | AFR | GWD | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0069 | SAS | PJL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG04228 | hp2 | a0008 | c0010 | t0001 | g0093 | SAS | STU | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18522 | hp2 | a0003 | c0004 | t0005 | g0023 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18612 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18906 | hp1 | a0004 | c0003 | t0004 | g0041 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18946 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18950 | hp1 | a0002 | c0002 | t0003 | g0050 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18950 | hp2 | a0002 | c0002 | t0014 | g0016 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18953 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0053 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18961 | hp2 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18964 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18971 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18977 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18988 | hp2 | a0002 | c0002 | t0003 | g0046 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18992 | hp2 | a0006 | c0006 | t0001 | g0013 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18994 | hp1 | a0002 | c0002 | t0003 | g0016 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19001 | hp2 | a0001 | c0001 | t0008 | g0104 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19009 | hp2 | a0006 | c0006 | t0001 | g0013 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19010 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0103 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0051 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19066 | hp2 | a0006 | c0006 | t0001 | g0013 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19077 | hp2 | a0002 | c0002 | t0003 | g0054 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19085 | hp2 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19091 | hp1 | a0002 | c0002 | t0003 | g0055 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19091 | hp2 | a0002 | c0002 | t0003 | g0049 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20905 | hp1 | a0003 | c0004 | t0005 | g0023 | SAS | GIH | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG02559 | hp2 | a0005 | c0005 | t0006 | g0022 | AFR | ACB | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA18955 | hp2 | a0002 | c0002 | t0003 | g0008 | EAS | JPT | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0017 | REF | REF | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0019 | REF | REF | AKR1E2_chr10_4821207_4853062 | AKR1E2 | chr10 | 4821207 | 4853062 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4830696
|
G | A | 1 | a0009 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.61G>A | p.Glu21Lys | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 179/1613 | 61/963 | 21/320 | chr10 | 4830696 | ||
| chr10:4830738
|
G | A | 1 | a0004 | 11 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(8): Show |
missense_variant | MODERATE | c.103G>A | p.Asp35Asn | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 221/1613 | 103/963 | 35/320 | chr10 | 4830738 | ||
| chr10:4830789
|
T | G | 1 | a0007 | 2 | HG02717.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.154T>G | p.Cys52Gly | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 272/1613 | 154/963 | 52/320 | chr10 | 4830789 | ||
| chr10:4833399
|
A | G | 1 | a0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
missense_variant | MODERATE | c.257A>G | p.Lys86Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/10 | 375/1613 | 257/963 | 86/320 | chr10 | 4833399 | ||
| chr10:4835679
|
C | G | 1 | a0005 | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.329C>G | p.Pro110Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/10 | 447/1613 | 329/963 | 110/320 | chr10 | 4835679 | ||
| chr10:4835787
|
C | G | 1 | a0008 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.437C>G | p.Thr146Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/10 | 555/1613 | 437/963 | 146/320 | chr10 | 4835787 | ||
| chr10:4847211
|
C | T | 1 | a0003 | 11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
stop_gained | HIGH | c.901C>T | p.Arg301* | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/10 | 1019/1613 | 901/963 | 301/320 | chr10 | 4847211 | ||
| chr10:4847493
|
A | G | 1 | a0006 | 3 | NA18992.hp2 NA19009.hp2 NA19066.hp2 |
missense_variant | MODERATE | c.926A>G | p.Lys309Arg | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 1044/1613 | 926/963 | 309/320 | chr10 | 4847493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4830695
|
C | A | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.60C>A | p.Thr20Thr | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 178/1613 | 60/963 | 20/320 | chr10 | 4830695 | ||
| chr10:4830695
|
C | T | 1 | a0001c0011 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.60C>T | p.Thr20Thr | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 178/1613 | 60/963 | 20/320 | chr10 | 4830695 | ||
| chr10:4830719
|
C | T | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.84C>T | p.Asp28Asp | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/10 | 202/1613 | 84/963 | 28/320 | chr10 | 4830719 | ||
| chr10:4837575
|
C | G | 1 | a0001c0009 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.576C>G | p.Thr192Thr | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/10 | 694/1613 | 576/963 | 192/320 | chr10 | 4837575 | ||
| chr10:4839743
|
A | G | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.597A>G | p.Pro199Pro | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/10 | 715/1613 | 597/963 | 199/320 | chr10 | 4839743 | ||
| chr10:4842450
|
T | C | 1 | a0002c0002 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
synonymous_variant | LOW | c.783T>C | p.Asn261Asn | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/10 | 901/1613 | 783/963 | 261/320 | chr10 | 4842450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4826253
|
G | T | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(12): Show | 266 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(263): Show |
5_prime_UTR_variant | MODIFIER | c.-72G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 72 | chr10 | 4826253 | |||||
| chr10:4826287
|
T | C | 1 | a0001c0001t0013 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 38 | chr10 | 4826287 | |||||
| chr10:4826287
|
T | TGCGGGGC others(1): Show |
2 | a0001c0001t0010a0002c0002t0012 | 3 | HG02155.hp2 HG02280.hp2 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-19_-12dupGGGGCGGC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 11 | INFO_REALIGN_3_PRIME | chr10 | 4826287 | ||||
| chr10:4826287
|
TGCGGGGC others(1): Show |
T | 1 | a0005c0005t0006 | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-19_-12delGGGGCGGC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 12 | INFO_REALIGN_3_PRIME | chr10 | 4826287 | ||||
| chr10:4826321
|
G | A | 1 | a0001c0001t0009 | 2 | HG02615.hp1 HG02630.hp1 |
5_prime_UTR_variant | MODIFIER | c.-4G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/10 | 4 | chr10 | 4826321 | |||||
| chr10:4847534
|
C | CA | 3 | a0002c0002t0003a0002c0002t0012a0002c0002t0014 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4_*5insA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 5 | chr10 | 4847534 | |||||
| chr10:4847538
|
T | A | 1 | a0003c0004t0007 | 3 | HG01928.hp2 HG01981.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 8 | chr10 | 4847538 | |||||
| chr10:4847540
|
C | T | 2 | a0001c0001t0004a0004c0003t0004 | 13 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*10C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 10 | chr10 | 4847540 | |||||
| chr10:4847578
|
T | C | 3 | a0002c0002t0003a0002c0002t0012a0002c0002t0014 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*48T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 48 | chr10 | 4847578 | |||||
| chr10:4847614
|
C | T | 3 | a0002c0002t0003a0002c0002t0012a0002c0002t0014 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*84C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 84 | chr10 | 4847614 | |||||
| chr10:4847672
|
C | G | 1 | a0001c0001t0011 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*142C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 142 | chr10 | 4847672 | |||||
| chr10:4847782
|
G | A | 3 | a0002c0002t0003a0002c0002t0012a0002c0002t0014 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*252G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 252 | chr10 | 4847782 | |||||
| chr10:4847882
|
C | T | 1 | a0001c0001t0015 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 352 | chr10 | 4847882 | |||||
| chr10:4847883
|
G | A | 1 | a0001c0001t0008 | 3 | NA18944.hp1 NA19001.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*353G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 353 | chr10 | 4847883 | |||||
| chr10:4847924
|
A | T | 3 | a0002c0002t0003a0002c0002t0012a0002c0002t0014 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*394A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 394 | chr10 | 4847924 | |||||
| chr10:4847953
|
C | T | 2 | a0003c0004t0005a0003c0004t0007 | 11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*423C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 423 | chr10 | 4847953 | |||||
| chr10:4847994
|
A | G | 3 | a0002c0002t0003a0002c0002t0012a0002c0002t0014 | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*464A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 10/10 | 464 | chr10 | 4847994 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:4826373
|
T | C | 5 | a0004c0003t0004g0010a0004c0003t0004g0020a0004c0003t0004g0041others(2): Show | 11 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.39+10T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826373 | ||||||
| chr10:4826589
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.39+226G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826589 | ||||||
| chr10:4826626
|
G | A | 1 | a0003c0004t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.39+263G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826626 | ||||||
| chr10:4826631
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+268T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826631 | ||||||
| chr10:4826678
|
T | C | 15 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(12): Show | 27 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.39+315T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826678 | ||||||
| chr10:4826687
|
C | G | 9 | a0001c0001t0001g0040a0003c0004t0005g0023a0003c0004t0005g0039others(6): Show | 12 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+324C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826687 | ||||||
| chr10:4826700
|
C | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+337C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826700 | ||||||
| chr10:4826729
|
G | T | 1 | a0001c0001t0001g0038 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.39+366G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826729 | ||||||
| chr10:4826799
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+436G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826799 | ||||||
| chr10:4826839
|
G | A | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.39+476G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826839 | ||||||
| chr10:4826896
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0002g0014a0001c0001t0002g0142others(1): Show | 9 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+533C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826896 | ||||||
| chr10:4826956
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.39+593G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826956 | ||||||
| chr10:4826981
|
T | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.39+618T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4826981 | ||||||
| chr10:4827051
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+688T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827051 | ||||||
| chr10:4827075
|
G | GA | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(62): Show | 154 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.39+730dupA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | |||||
| chr10:4827075
|
G | GAA | 3 | a0001c0001t0001g0011a0001c0001t0001g0070a0003c0004t0005g0144 | 7 | HG01257.hp1 HG03490.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+729_39+730dupAA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | |||||
| chr10:4827075
|
G | GAAA | 9 | a0001c0001t0001g0004a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 19 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(16): Show |
intron_variant | MODIFIER | c.39+728_39+730dupAA others(1): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | |||||
| chr10:4827075
|
G | GAAAA | 5 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG02486.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+727_39+730dupAA others(2): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | |||||
| chr10:4827075
|
GAAAAAA | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0140 | 10 | HG00558.hp1 HG00621.hp2 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+725_39+730delAA others(4): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | |||||
| chr10:4827075
|
GAAAAAAA | G | 3 | a0002c0002t0003g0008a0002c0002t0003g0025a0002c0002t0003g0053 | 10 | NA18941.hp1 NA18946.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.39+724_39+730delAA others(5): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | |||||
| chr10:4827075
|
GAAAAAAA others(1): Show |
G | 5 | a0001c0001t0001g0040a0001c0001t0002g0014a0001c0001t0002g0141others(2): Show | 10 | HG01891.hp1 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+723_39+730delAA others(6): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827075 | |||||
| chr10:4827088
|
A | AG | 7 | a0001c0001t0001g0139a0001c0001t0004g0037a0004c0003t0004g0010others(4): Show | 14 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.39+725_39+726insG | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827088 | ||||||
| chr10:4827301
|
T | A | 1 | a0004c0003t0004g0020 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.39+938T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827301 | ||||||
| chr10:4827306
|
ATTG | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0105a0001c0001t0001g0138 | 12 | HG00140.hp1 HG01069.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.39+946_39+948delGT others(1): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827306 | |||||
| chr10:4827318
|
AAGATGTT others(177): Show |
A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+957_39+1140del | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827318 | |||||
| chr10:4827422
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.39+1059G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827422 | ||||||
| chr10:4827604
|
T | TA | 8 | a0001c0001t0001g0062a0001c0001t0001g0139a0001c0001t0004g0037others(5): Show | 15 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+1252dupA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827604 | |||||
| chr10:4827604
|
TA | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1252delA | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827604 | |||||
| chr10:4827610
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.39+1247A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827610 | ||||||
| chr10:4827696
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00597.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.39+1333G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827696 | ||||||
| chr10:4827706
|
ATAT | A | 2 | a0002c0002t0003g0016a0002c0002t0014g0016 | 4 | NA18612.hp1 NA18950.hp2 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1348_39+1350del others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827706 | |||||
| chr10:4827730
|
C | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1367C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827730 | ||||||
| chr10:4827781
|
C | T | 1 | a0002c0002t0003g0052 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.39+1418C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827781 | ||||||
| chr10:4827794
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1431G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827794 | ||||||
| chr10:4827839
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.39+1476G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827839 | ||||||
| chr10:4827849
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.39+1486T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827849 | ||||||
| chr10:4827893
|
G | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1530G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4827893 | ||||||
| chr10:4827958
|
ATATTC | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1600_39+1604del others(5): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4827958 | |||||
| chr10:4828032
|
C | A | 3 | a0001c0001t0001g0040a0001c0001t0002g0014a0001c0001t0002g0142 | 8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.39+1669C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828032 | ||||||
| chr10:4828050
|
C | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(126): Show | 306 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.39+1687C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828050 | ||||||
| chr10:4828148
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.39+1785A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828148 | ||||||
| chr10:4828250
|
G | A | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.39+1887G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828250 | ||||||
| chr10:4828328
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 303 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.39+1965G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828328 | ||||||
| chr10:4828452
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 277 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.39+2089G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828452 | ||||||
| chr10:4828650
|
A | C | 2 | a0001c0001t0001g0013a0006c0006t0001g0013 | 5 | HG00558.hp2 HG00597.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-2025A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828650 | ||||||
| chr10:4828662
|
C | T | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.40-2013C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828662 | ||||||
| chr10:4828721
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.40-1954T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828721 | ||||||
| chr10:4828814
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-1861G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828814 | ||||||
| chr10:4828860
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(126): Show | 306 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.40-1815G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828860 | ||||||
| chr10:4828927
|
G | A | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.40-1748G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4828927 | ||||||
| chr10:4828981
|
TATC | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-1689_40-1687del others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4828981 | |||||
| chr10:4829023
|
C | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(126): Show | 306 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.40-1652C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829023 | ||||||
| chr10:4829058
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1617C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829058 | ||||||
| chr10:4829242
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1433G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829242 | ||||||
| chr10:4829264
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1411T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829264 | ||||||
| chr10:4829399
|
A | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1276A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829399 | ||||||
| chr10:4829414
|
G | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-1261G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829414 | ||||||
| chr10:4829462
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.40-1213T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829462 | ||||||
| chr10:4829473
|
G | A | 9 | a0003c0004t0005g0023a0003c0004t0005g0039a0003c0004t0005g0045others(6): Show | 11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.40-1202G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829473 | ||||||
| chr10:4829515
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.40-1160T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829515 | ||||||
| chr10:4829551
|
A | AT | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-1117dupT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4829551 | |||||
| chr10:4829590
|
C | CTT | 16 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(13): Show | 28 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.40-1078_40-1077dup others(2): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4829590 | |||||
| chr10:4829590
|
C | T | 1 | a0002c0002t0003g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40-1085C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829590 | ||||||
| chr10:4829605
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0009g0027 | 3 | HG02615.hp1 HG02630.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.40-1070C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829605 | ||||||
| chr10:4829696
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 313 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.40-979G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829696 | ||||||
| chr10:4829767
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.40-908G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829767 | ||||||
| chr10:4829930
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-745C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4829930 | ||||||
| chr10:4830021
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0124a0001c0001t0011g0074 | 4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-654G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830021 | ||||||
| chr10:4830022
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-653A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830022 | ||||||
| chr10:4830053
|
C | T | 14 | a0001c0001t0001g0004a0001c0001t0001g0058a0001c0001t0001g0059others(11): Show | 24 | HG01261.hp2 HG02109.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.40-622C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830053 | ||||||
| chr10:4830071
|
A | C | 1 | a0002c0002t0003g0024 | 2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.40-604A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830071 | ||||||
| chr10:4830131
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0124a0001c0001t0002g0143others(1): Show | 5 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-544C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830131 | ||||||
| chr10:4830229
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-446A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830229 | ||||||
| chr10:4830240
|
A | G | 2 | a0001c0001t0009g0027a0007c0007t0002g0031 | 4 | HG02615.hp1 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-435A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830240 | ||||||
| chr10:4830256
|
A | G | 1 | a0001c0001t0008g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.40-419A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830256 | ||||||
| chr10:4830332
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.40-343A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830332 | ||||||
| chr10:4830347
|
T | TC | 10 | a0001c0001t0001g0135a0003c0004t0005g0023a0003c0004t0005g0039others(7): Show | 12 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.40-328_40-327insC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830347 | ||||||
| chr10:4830364
|
C | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.40-311C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830364 | ||||||
| chr10:4830381
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(151): Show | 353 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.40-294G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830381 | ||||||
| chr10:4830425
|
C | T | 7 | a0001c0001t0001g0139a0001c0001t0004g0037a0004c0003t0004g0010others(4): Show | 14 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-250C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830425 | ||||||
| chr10:4830459
|
GT | G | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.40-207delT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr10 | 4830459 | |||||
| chr10:4830495
|
T | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-180T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830495 | ||||||
| chr10:4830577
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.40-98T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830577 | ||||||
| chr10:4830630
|
A | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-45A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830630 | ||||||
| chr10:4830640
|
C | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.40-35C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 1/9 | chr10 | 4830640 | ||||||
| chr10:4830845
|
A | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
splice_region_variant&intron_variant | LOW | c.207+3A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4830845 | ||||||
| chr10:4830914
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0017others(7): Show | 31 | HG00140.hp1 HG01069.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+72T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4830914 | ||||||
| chr10:4831072
|
A | T | 2 | a0001c0001t0008g0103a0002c0002t0003g0053 | 2 | NA18954.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.207+230A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831072 | ||||||
| chr10:4831331
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.207+489T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831331 | ||||||
| chr10:4831350
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+508G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831350 | ||||||
| chr10:4831466
|
G | A | 2 | a0001c0001t0002g0143a0001c0001t0009g0027 | 3 | HG02615.hp1 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.207+624G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831466 | ||||||
| chr10:4831492
|
A | C | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+650A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831492 | ||||||
| chr10:4831493
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+651G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831493 | ||||||
| chr10:4831511
|
G | C | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+669G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831511 | ||||||
| chr10:4831530
|
G | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+688G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831530 | ||||||
| chr10:4831534
|
C | T | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+692C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831534 | ||||||
| chr10:4831565
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.207+723A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831565 | ||||||
| chr10:4831574
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+732T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831574 | ||||||
| chr10:4831734
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+892T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831734 | ||||||
| chr10:4831744
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+902T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831744 | ||||||
| chr10:4831745
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+903G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831745 | ||||||
| chr10:4831752
|
A | G | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+910A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831752 | ||||||
| chr10:4831827
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+985A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831827 | ||||||
| chr10:4831852
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.207+1010A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831852 | ||||||
| chr10:4831876
|
A | G | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.207+1034A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831876 | ||||||
| chr10:4831933
|
A | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.207+1091A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4831933 | ||||||
| chr10:4832022
|
G | T | 9 | a0003c0004t0005g0023a0003c0004t0005g0039a0003c0004t0005g0045others(6): Show | 11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.207+1180G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832022 | ||||||
| chr10:4832120
|
G | GT | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 313 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.208-1229dupT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 4832120 | |||||
| chr10:4832208
|
C | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.208-1142C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832208 | ||||||
| chr10:4832335
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.208-1015G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832335 | ||||||
| chr10:4832397
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-953G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832397 | ||||||
| chr10:4832520
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-830G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832520 | ||||||
| chr10:4832602
|
A | G | 9 | a0003c0004t0005g0023a0003c0004t0005g0039a0003c0004t0005g0045others(6): Show | 11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-748A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832602 | ||||||
| chr10:4832607
|
A | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-743A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832607 | ||||||
| chr10:4832607
|
A | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-743A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832607 | ||||||
| chr10:4832644
|
A | G | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.208-706A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832644 | ||||||
| chr10:4832679
|
G | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(22): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.208-671G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832679 | ||||||
| chr10:4832724
|
TTTTACTT others(8): Show |
T | 24 | a0001c0001t0004g0037a0001c0001t0009g0027a0002c0002t0003g0008others(21): Show | 44 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.208-601_208-587del others(15): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr10 | 4832724 | |||||
| chr10:4832875
|
G | A | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.208-475G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832875 | ||||||
| chr10:4832880
|
C | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-470C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832880 | ||||||
| chr10:4832958
|
T | C | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.208-392T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832958 | ||||||
| chr10:4832997
|
G | A | 2 | a0002c0002t0003g0047a0002c0002t0003g0048 | 2 | HG00642.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.208-353G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4832997 | ||||||
| chr10:4833043
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.208-307T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833043 | ||||||
| chr10:4833070
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.208-280A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833070 | ||||||
| chr10:4833079
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.208-271A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833079 | ||||||
| chr10:4833084
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-266C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833084 | ||||||
| chr10:4833172
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.208-178C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833172 | ||||||
| chr10:4833208
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.208-142C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833208 | ||||||
| chr10:4833217
|
T | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.208-133T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833217 | ||||||
| chr10:4833249
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.208-101G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833249 | ||||||
| chr10:4833263
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.208-87C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 2/9 | chr10 | 4833263 | ||||||
| chr10:4833472
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.324+6G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833472 | ||||||
| chr10:4833637
|
C | A | 1 | a0001c0001t0001g0083 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.324+171C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833637 | ||||||
| chr10:4833682
|
G | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.324+216G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833682 | ||||||
| chr10:4833702
|
G | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(18): Show | 61 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.324+236G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833702 | ||||||
| chr10:4833731
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.324+265A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833731 | ||||||
| chr10:4833987
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.324+521A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4833987 | ||||||
| chr10:4834028
|
C | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+562C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834028 | ||||||
| chr10:4834030
|
T | G | 1 | a0002c0002t0003g0054 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.324+564T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834030 | ||||||
| chr10:4834154
|
C | T | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+688C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834154 | ||||||
| chr10:4834183
|
G | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.324+717G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834183 | ||||||
| chr10:4834211
|
C | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+745C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834211 | ||||||
| chr10:4834377
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.324+911T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834377 | ||||||
| chr10:4834382
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.324+916G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834382 | ||||||
| chr10:4834434
|
A | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 157 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.324+968A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834434 | ||||||
| chr10:4834691
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.325-984T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834691 | ||||||
| chr10:4834768
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-907G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834768 | ||||||
| chr10:4834779
|
A | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-896A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834779 | ||||||
| chr10:4834781
|
A | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.325-894A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834781 | ||||||
| chr10:4834898
|
A | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-777A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834898 | ||||||
| chr10:4834909
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.325-766C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834909 | ||||||
| chr10:4834923
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.325-752G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4834923 | ||||||
| chr10:4835121
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.325-554A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835121 | ||||||
| chr10:4835167
|
A | G | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-508A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835167 | ||||||
| chr10:4835200
|
A | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.325-475A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835200 | ||||||
| chr10:4835267
|
A | C | 1 | a0001c0001t0001g0028 | 2 | HG01106.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.325-408A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835267 | ||||||
| chr10:4835330
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.325-345G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835330 | ||||||
| chr10:4835388
|
T | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-287T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835388 | ||||||
| chr10:4835443
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.325-232C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835443 | ||||||
| chr10:4835524
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.325-151T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835524 | ||||||
| chr10:4835544
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.325-131G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835544 | ||||||
| chr10:4835618
|
G | T | 2 | a0001c0001t0001g0073a0001c0001t0009g0027 | 3 | HG02615.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.325-57G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835618 | ||||||
| chr10:4835622
|
T | TTTTTG | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(49): Show | 149 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.325-33_325-29dupGT others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 4835622 | |||||
| chr10:4835624
|
T | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-51T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835624 | ||||||
| chr10:4835625
|
T | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.325-50T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835625 | ||||||
| chr10:4835627
|
G | T | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-48G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835627 | ||||||
| chr10:4835628
|
T | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.325-47T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835628 | ||||||
| chr10:4835633
|
TTTTG | T | 16 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(13): Show | 28 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.325-38_325-35delGT others(2): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr10 | 4835633 | |||||
| chr10:4835642
|
G | T | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.325-33G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 3/9 | chr10 | 4835642 | ||||||
| chr10:4835889
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+80G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4835889 | ||||||
| chr10:4835940
|
A | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.459+131A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4835940 | ||||||
| chr10:4835955
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+146C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4835955 | ||||||
| chr10:4836012
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(39): Show | 97 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.459+203T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836012 | ||||||
| chr10:4836040
|
A | G | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+231A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836040 | ||||||
| chr10:4836083
|
T | G | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+274T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836083 | ||||||
| chr10:4836123
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+314C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836123 | ||||||
| chr10:4836127
|
T | C | 18 | a0001c0001t0009g0027a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 31 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+318T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836127 | ||||||
| chr10:4836129
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+320C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836129 | ||||||
| chr10:4836217
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+408T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836217 | ||||||
| chr10:4836218
|
C | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+409C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836218 | ||||||
| chr10:4836239
|
A | G | 10 | a0001c0001t0001g0135a0003c0004t0005g0023a0003c0004t0005g0039others(7): Show | 12 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+430A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836239 | ||||||
| chr10:4836349
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+540A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836349 | ||||||
| chr10:4836372
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.459+563G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836372 | ||||||
| chr10:4836403
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 313 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.459+594T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836403 | ||||||
| chr10:4836410
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0013g0069 | 2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.459+601C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836410 | ||||||
| chr10:4836472
|
A | G | 14 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0024others(11): Show | 24 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.459+663A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836472 | ||||||
| chr10:4836514
|
G | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.459+705G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836514 | ||||||
| chr10:4836543
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.459+734G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836543 | ||||||
| chr10:4836687
|
G | A | 16 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0106others(13): Show | 53 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.460-772G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836687 | ||||||
| chr10:4836731
|
G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 313 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.460-728G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836731 | ||||||
| chr10:4836739
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-720A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836739 | ||||||
| chr10:4836769
|
G | A | 2 | a0002c0002t0003g0054a0002c0002t0003g0055 | 2 | NA19077.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.460-690G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836769 | ||||||
| chr10:4836780
|
G | A | 18 | a0001c0001t0001g0063a0001c0001t0001g0135a0001c0001t0004g0037others(15): Show | 27 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-679G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836780 | ||||||
| chr10:4836834
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-625C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836834 | ||||||
| chr10:4836903
|
A | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 163 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.460-556A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4836903 | ||||||
| chr10:4837055
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.460-404G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837055 | ||||||
| chr10:4837180
|
C | G | 10 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.460-279C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837180 | ||||||
| chr10:4837188
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-271C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837188 | ||||||
| chr10:4837221
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.460-238T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837221 | ||||||
| chr10:4837233
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.460-226A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837233 | ||||||
| chr10:4837273
|
T | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 313 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(310): Show |
intron_variant | MODIFIER | c.460-186T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837273 | ||||||
| chr10:4837376
|
A | C | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.460-83A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837376 | ||||||
| chr10:4837447
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.460-12G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 4/9 | chr10 | 4837447 | ||||||
| chr10:4837723
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+142T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4837723 | ||||||
| chr10:4837885
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+304T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4837885 | ||||||
| chr10:4837971
|
G | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.582+390G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4837971 | ||||||
| chr10:4838046
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.582+465C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838046 | ||||||
| chr10:4838049
|
T | C | 2 | a0001c0001t0002g0075a0001c0001t0002g0126 | 2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.582+468T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838049 | ||||||
| chr10:4838099
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+518T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838099 | ||||||
| chr10:4838130
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.582+549A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838130 | ||||||
| chr10:4838182
|
T | C | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(125): Show | 305 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.582+601T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838182 | ||||||
| chr10:4838207
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+626G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838207 | ||||||
| chr10:4838232
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+651G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838232 | ||||||
| chr10:4838244
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.582+663A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838244 | ||||||
| chr10:4838282
|
T | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.582+701T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838282 | ||||||
| chr10:4838423
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.582+842T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838423 | ||||||
| chr10:4838468
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.582+887G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838468 | ||||||
| chr10:4838488
|
G | A | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.582+907G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838488 | ||||||
| chr10:4838496
|
T | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0088others(17): Show | 37 | HG00621.hp1 HG00642.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.582+915T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838496 | ||||||
| chr10:4838689
|
C | T | 1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.583-1040C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838689 | ||||||
| chr10:4838936
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0058 | 3 | HG02559.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.583-793G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4838936 | ||||||
| chr10:4839022
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-707C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839022 | ||||||
| chr10:4839299
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0015g0017 | 4 | HG01952.hp1 HG02004.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-430A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839299 | ||||||
| chr10:4839354
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-375G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839354 | ||||||
| chr10:4839419
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.583-310G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839419 | ||||||
| chr10:4839453
|
TTATC | T | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.583-274_583-271del others(4): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr10 | 4839453 | |||||
| chr10:4839490
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.583-239G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839490 | ||||||
| chr10:4839507
|
A | C | 1 | a0001c0001t0002g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.583-222A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839507 | ||||||
| chr10:4839586
|
C | T | 2 | a0001c0001t0002g0032a0001c0001t0002g0124 | 3 | HG01243.hp1 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.583-143C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839586 | ||||||
| chr10:4839596
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.583-133G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839596 | ||||||
| chr10:4839631
|
C | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-98C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839631 | ||||||
| chr10:4839654
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.583-75C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839654 | ||||||
| chr10:4839675
|
C | T | 1 | a0004c0003t0004g0020 | 3 | HG01167.hp2 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.583-54C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839675 | ||||||
| chr10:4839686
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.583-43C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 5/9 | chr10 | 4839686 | ||||||
| chr10:4839889
|
T | C | 1 | a0002c0002t0003g0050 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.680+63T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4839889 | ||||||
| chr10:4839903
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.680+77C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4839903 | ||||||
| chr10:4840108
|
A | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0124a0001c0001t0011g0074 | 4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+282A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840108 | ||||||
| chr10:4840118
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.680+292C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840118 | ||||||
| chr10:4840173
|
G | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(22): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.680+347G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840173 | ||||||
| chr10:4840197
|
C | T | 11 | a0002c0002t0003g0008a0002c0002t0003g0016a0002c0002t0003g0025others(8): Show | 20 | NA18612.hp1 NA18941.hp1 NA18946.hp1 others(17): Show |
intron_variant | MODIFIER | c.680+371C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840197 | ||||||
| chr10:4840215
|
G | C | 1 | a0001c0001t0002g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.680+389G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840215 | ||||||
| chr10:4840306
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.680+480C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840306 | ||||||
| chr10:4840341
|
A | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.680+515A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840341 | ||||||
| chr10:4840342
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.680+516G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840342 | ||||||
| chr10:4840365
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.680+539G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840365 | ||||||
| chr10:4840521
|
A | G | 5 | a0001c0001t0001g0139a0001c0001t0002g0032a0001c0001t0002g0124others(2): Show | 6 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+695A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840521 | ||||||
| chr10:4840532
|
G | C | 6 | a0001c0001t0004g0037a0004c0003t0004g0010a0004c0003t0004g0020others(3): Show | 14 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+706G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840532 | ||||||
| chr10:4840594
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.680+768C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840594 | ||||||
| chr10:4840628
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.680+802C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840628 | ||||||
| chr10:4840782
|
T | G | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.680+956T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840782 | ||||||
| chr10:4840866
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.681-919G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840866 | ||||||
| chr10:4840900
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.681-885G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4840900 | ||||||
| chr10:4841132
|
G | C | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.681-653G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841132 | ||||||
| chr10:4841190
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-595C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841190 | ||||||
| chr10:4841195
|
C | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-590C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841195 | ||||||
| chr10:4841274
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.681-511C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841274 | ||||||
| chr10:4841282
|
T | G | 1 | a0001c0001t0002g0129 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.681-503T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841282 | ||||||
| chr10:4841322
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0002g0014a0001c0001t0002g0142 | 8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.681-463A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841322 | ||||||
| chr10:4841475
|
C | CA | 41 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(38): Show | 95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.681-310_681-309ins others(1): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841475 | ||||||
| chr10:4841516
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-269G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841516 | ||||||
| chr10:4841533
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-252T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841533 | ||||||
| chr10:4841544
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-241A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841544 | ||||||
| chr10:4841558
|
T | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-227T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841558 | ||||||
| chr10:4841572
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.681-213G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841572 | ||||||
| chr10:4841678
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.681-107T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841678 | ||||||
| chr10:4841755
|
G | T | 1 | a0001c0001t0002g0142 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.681-30G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 6/9 | chr10 | 4841755 | ||||||
| chr10:4841874
|
G | C | 1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.753+17G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841874 | ||||||
| chr10:4841884
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+27A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841884 | ||||||
| chr10:4841907
|
A | G | 1 | a0003c0004t0005g0147 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.753+50A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841907 | ||||||
| chr10:4841912
|
C | T | 1 | a0002c0002t0003g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.753+55C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841912 | ||||||
| chr10:4841968
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.753+111G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4841968 | ||||||
| chr10:4842019
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+162C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842019 | ||||||
| chr10:4842025
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+168T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842025 | ||||||
| chr10:4842052
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+195C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842052 | ||||||
| chr10:4842095
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0070a0006c0006t0001g0013 | 6 | HG00558.hp2 HG00597.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.753+238C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842095 | ||||||
| chr10:4842130
|
A | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.753+273A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842130 | ||||||
| chr10:4842234
|
C | G | 7 | a0001c0001t0001g0139a0001c0001t0002g0032a0001c0001t0002g0075others(4): Show | 8 | HG01243.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-187C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842234 | ||||||
| chr10:4842255
|
G | T | 9 | a0003c0004t0005g0023a0003c0004t0005g0039a0003c0004t0005g0045others(6): Show | 11 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.754-166G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 7/9 | chr10 | 4842255 | ||||||
| chr10:4842529
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+25G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842529 | ||||||
| chr10:4842531
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.837+27C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842531 | ||||||
| chr10:4842592
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(133): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.837+88T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842592 | ||||||
| chr10:4842593
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.837+89G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842593 | ||||||
| chr10:4842608
|
A | G | 41 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(38): Show | 95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.837+104A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842608 | ||||||
| chr10:4842616
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+112T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842616 | ||||||
| chr10:4842618
|
C | T | 3 | a0001c0001t0002g0032a0001c0001t0002g0124a0001c0001t0011g0074 | 4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+114C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842618 | ||||||
| chr10:4842652
|
T | TC | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+151dupC | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4842652 | |||||
| chr10:4842736
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.837+232A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842736 | ||||||
| chr10:4842771
|
T | A | 41 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(38): Show | 95 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.837+267T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842771 | ||||||
| chr10:4842854
|
G | A | 15 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0058others(12): Show | 26 | HG01261.hp2 HG02109.hp2 HG02132.hp1 others(23): Show |
intron_variant | MODIFIER | c.837+350G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842854 | ||||||
| chr10:4842858
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+354A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4842858 | ||||||
| chr10:4842941
|
CT | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.837+440delT | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4842941 | |||||
| chr10:4843025
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+521C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843025 | ||||||
| chr10:4843026
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.837+522G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843026 | ||||||
| chr10:4843039
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+535A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843039 | ||||||
| chr10:4843056
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0091 | 2 | HG02071.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.837+552T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843056 | ||||||
| chr10:4843136
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.837+632A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843136 | ||||||
| chr10:4843151
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.837+647C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843151 | ||||||
| chr10:4843207
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+703C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843207 | ||||||
| chr10:4843302
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0002g0014a0001c0001t0002g0142 | 8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+798G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843302 | ||||||
| chr10:4843313
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+809G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843313 | ||||||
| chr10:4843321
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.837+817A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843321 | ||||||
| chr10:4843337
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.837+833C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843337 | ||||||
| chr10:4843340
|
A | G | 2 | a0003c0004t0005g0144a0003c0004t0005g0146 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.837+836A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843340 | ||||||
| chr10:4843344
|
A | C | 1 | a0001c0001t0002g0035 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.837+840A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843344 | ||||||
| chr10:4843423
|
T | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0062others(7): Show | 20 | HG01261.hp2 HG02132.hp1 HG02738.hp2 others(17): Show |
intron_variant | MODIFIER | c.837+919T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843423 | ||||||
| chr10:4843428
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.837+924G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843428 | ||||||
| chr10:4843458
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+954T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843458 | ||||||
| chr10:4843614
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 157 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.837+1110G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843614 | ||||||
| chr10:4843618
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.837+1114T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843618 | ||||||
| chr10:4843642
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1138A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843642 | ||||||
| chr10:4843651
|
G | T | 3 | a0001c0001t0001g0040a0001c0001t0002g0014a0001c0001t0002g0142 | 8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+1147G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843651 | ||||||
| chr10:4843727
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1223A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843727 | ||||||
| chr10:4843742
|
A | C | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.837+1238A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843742 | ||||||
| chr10:4843743
|
C | G | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.837+1239C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843743 | ||||||
| chr10:4843829
|
C | T | 1 | a0007c0007t0002g0031 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.837+1325C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843829 | ||||||
| chr10:4843848
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.837+1344G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843848 | ||||||
| chr10:4843908
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1404G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843908 | ||||||
| chr10:4843925
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1421A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843925 | ||||||
| chr10:4843976
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1472A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4843976 | ||||||
| chr10:4844059
|
G | A | 2 | a0004c0003t0004g0041a0004c0003t0004g0042 | 2 | HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.837+1555G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844059 | ||||||
| chr10:4844091
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.837+1587C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844091 | ||||||
| chr10:4844093
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.837+1589C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844093 | ||||||
| chr10:4844125
|
A | C | 1 | a0001c0001t0008g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.837+1621A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844125 | ||||||
| chr10:4844126
|
G | T | 1 | a0001c0001t0008g0103 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.837+1622G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844126 | ||||||
| chr10:4844136
|
C | T | 1 | a0001c0001t0010g0026 | 2 | HG02280.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.837+1632C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844136 | ||||||
| chr10:4844171
|
G | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.837+1667G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844171 | ||||||
| chr10:4844225
|
A | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1721A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844225 | ||||||
| chr10:4844237
|
G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.837+1733G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844237 | ||||||
| chr10:4844314
|
A | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0106others(13): Show | 53 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.837+1810A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844314 | ||||||
| chr10:4844337
|
C | T | 21 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(18): Show | 61 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.837+1833C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844337 | ||||||
| chr10:4844409
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.837+1905C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844409 | ||||||
| chr10:4844410
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1906G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844410 | ||||||
| chr10:4844427
|
G | A | 1 | a0004c0003t0004g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.837+1923G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844427 | ||||||
| chr10:4844431
|
T | C | 1 | a0001c0001t0001g0029 | 2 | HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.837+1927T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844431 | ||||||
| chr10:4844449
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1945T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844449 | ||||||
| chr10:4844453
|
T | G | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.837+1949T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844453 | ||||||
| chr10:4844459
|
G | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+1955G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844459 | ||||||
| chr10:4844535
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+2031G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844535 | ||||||
| chr10:4844540
|
G | C | 4 | a0003c0004t0005g0039a0003c0004t0005g0144a0003c0004t0005g0146others(1): Show | 5 | HG01175.hp2 HG01346.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.837+2036G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844540 | ||||||
| chr10:4844693
|
G | A | 1 | a0005c0005t0006g0022 | 3 | HG02559.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.837+2189G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844693 | ||||||
| chr10:4844713
|
G | GTGAGCTA others(157): Show |
17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.837+2249_837+2250i others(166): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4844713 | |||||
| chr10:4844754
|
G | A | 1 | a0003c0004t0007g0145 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.837+2250G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844754 | ||||||
| chr10:4844865
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0081 | 3 | NA18973.hp2 NA18998.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.838-2283C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844865 | ||||||
| chr10:4844866
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.838-2282G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844866 | ||||||
| chr10:4844900
|
C | T | 18 | a0001c0001t0001g0122a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 30 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.838-2248C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844900 | ||||||
| chr10:4844931
|
G | T | 3 | a0001c0001t0001g0108a0005c0005t0006g0022a0005c0005t0006g0109 | 5 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.838-2217G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844931 | ||||||
| chr10:4844950
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2198T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4844950 | ||||||
| chr10:4845001
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.838-2147G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845001 | ||||||
| chr10:4845063
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2085G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845063 | ||||||
| chr10:4845103
|
C | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2045C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845103 | ||||||
| chr10:4845104
|
C | T | 18 | a0001c0001t0001g0066a0002c0002t0003g0008a0002c0002t0003g0015others(15): Show | 30 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.838-2044C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845104 | ||||||
| chr10:4845130
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-2018T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845130 | ||||||
| chr10:4845148
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.838-2000C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845148 | ||||||
| chr10:4845164
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1984A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845164 | ||||||
| chr10:4845199
|
A | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(55): Show | 125 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.838-1949A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845199 | ||||||
| chr10:4845202
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1946C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845202 | ||||||
| chr10:4845207
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1941C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845207 | ||||||
| chr10:4845236
|
A | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG02109.hp2 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-1912A>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845236 | ||||||
| chr10:4845268
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1880G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845268 | ||||||
| chr10:4845278
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 181 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.838-1870G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845278 | ||||||
| chr10:4845279
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1869A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845279 | ||||||
| chr10:4845297
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.838-1851C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845297 | ||||||
| chr10:4845329
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1819G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845329 | ||||||
| chr10:4845340
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(68): Show | 182 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.838-1808C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845340 | ||||||
| chr10:4845373
|
C | T | 5 | a0001c0001t0001g0139a0001c0001t0002g0032a0001c0001t0002g0124others(2): Show | 6 | HG01243.hp1 HG02886.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.838-1775C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845373 | ||||||
| chr10:4845390
|
C | T | 2 | a0005c0005t0006g0022a0005c0005t0006g0109 | 4 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-1758C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845390 | ||||||
| chr10:4845398
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.838-1750G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845398 | ||||||
| chr10:4845442
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1706T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845442 | ||||||
| chr10:4845448
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1700T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845448 | ||||||
| chr10:4845453
|
A | AGGGCTGC others(55): Show |
1 | a0001c0001t0002g0143 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.838-1690_838-1629d others(64): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4845453 | |||||
| chr10:4845453
|
AGGGCTGC others(24): Show |
A | 88 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 211 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.838-1659_838-1629d others(33): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4845453 | |||||
| chr10:4845546
|
G | A | 2 | a0004c0003t0004g0010a0004c0003t0004g0020 | 8 | HG00735.hp1 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.838-1602G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845546 | ||||||
| chr10:4845621
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1527C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845621 | ||||||
| chr10:4845664
|
G | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0058 | 3 | HG02559.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.838-1484G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845664 | ||||||
| chr10:4845680
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.838-1468G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845680 | ||||||
| chr10:4845698
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.838-1450C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845698 | ||||||
| chr10:4845724
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.838-1424G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845724 | ||||||
| chr10:4845743
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1405T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845743 | ||||||
| chr10:4845796
|
G | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.838-1352G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845796 | ||||||
| chr10:4845813
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.838-1335G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845813 | ||||||
| chr10:4845892
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.838-1256G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845892 | ||||||
| chr10:4845895
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.838-1253G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845895 | ||||||
| chr10:4845908
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.838-1240C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845908 | ||||||
| chr10:4845948
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1200A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845948 | ||||||
| chr10:4845957
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1191A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4845957 | ||||||
| chr10:4846002
|
C | T | 1 | a0007c0007t0002g0031 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838-1146C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846002 | ||||||
| chr10:4846030
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(22): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.838-1118C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846030 | ||||||
| chr10:4846087
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1061T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846087 | ||||||
| chr10:4846142
|
A | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1006A>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846142 | ||||||
| chr10:4846157
|
G | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0086a0001c0001t0001g0089 | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-991G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846157 | ||||||
| chr10:4846233
|
A | G | 2 | a0001c0001t0001g0114a0009c0008t0001g0113 | 2 | HG02523.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.838-915A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846233 | ||||||
| chr10:4846263
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-885G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846263 | ||||||
| chr10:4846284
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-864C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846284 | ||||||
| chr10:4846290
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0092 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.838-858G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846290 | ||||||
| chr10:4846318
|
G | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-830G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846318 | ||||||
| chr10:4846361
|
G | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(48): Show | 148 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.838-787G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846361 | ||||||
| chr10:4846382
|
C | G | 1 | a0001c0001t0008g0104 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.838-766C>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846382 | ||||||
| chr10:4846399
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.838-749T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846399 | ||||||
| chr10:4846449
|
C | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-699C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846449 | ||||||
| chr10:4846454
|
G | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0124a0001c0001t0011g0074 | 4 | HG01243.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.838-694G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846454 | ||||||
| chr10:4846492
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.838-656T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846492 | ||||||
| chr10:4846530
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.838-618G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846530 | ||||||
| chr10:4846549
|
C | CTTT | 16 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(13): Show | 27 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.838-587_838-585dup others(3): Show |
AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr10 | 4846549 | |||||
| chr10:4846590
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0071others(21): Show | 66 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.838-558A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846590 | ||||||
| chr10:4846614
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-534C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846614 | ||||||
| chr10:4846651
|
T | C | 1 | a0008c0010t0001g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.838-497T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846651 | ||||||
| chr10:4846717
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.838-431T>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846717 | ||||||
| chr10:4846769
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-379C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846769 | ||||||
| chr10:4846824
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 210 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.838-324G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846824 | ||||||
| chr10:4846828
|
A | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-320A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846828 | ||||||
| chr10:4846833
|
C | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-315C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846833 | ||||||
| chr10:4846838
|
C | A | 1 | a0007c0007t0002g0031 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.838-310C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846838 | ||||||
| chr10:4846844
|
G | A | 1 | a0009c0008t0001g0113 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.838-304G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846844 | ||||||
| chr10:4846920
|
G | C | 1 | a0001c0001t0002g0033 | 2 | HG02040.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.838-228G>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846920 | ||||||
| chr10:4846947
|
C | A | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-201C>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4846947 | ||||||
| chr10:4847006
|
G | A | 1 | a0001c0001t0009g0027 | 2 | HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.838-142G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847006 | ||||||
| chr10:4847069
|
C | T | 1 | a0001c0001t0002g0034 | 2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.838-79C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847069 | ||||||
| chr10:4847073
|
G | A | 14 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(11): Show | 25 | HG02015.hp1 HG02129.hp1 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.838-75G>A | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847073 | ||||||
| chr10:4847115
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.838-33A>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 8/9 | chr10 | 4847115 | ||||||
| chr10:4847283
|
G | T | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.920+53G>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847283 | ||||||
| chr10:4847312
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.920+82C>T | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847312 | ||||||
| chr10:4847333
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(110): Show | 279 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.920+103T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847333 | ||||||
| chr10:4847448
|
T | C | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-40T>C | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847448 | ||||||
| chr10:4847470
|
T | G | 17 | a0002c0002t0003g0008a0002c0002t0003g0015a0002c0002t0003g0016others(14): Show | 29 | HG00642.hp1 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-18T>G | AKR1E2 | ENSG00000165568.18 | transcript | ENST00000298375.12 | protein_coding | 9/9 | chr10 | 4847470 |