Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55500 |
|---|---|
| ensemblid | ENSG00000139163.16 |
| hgncid | 24649 |
| symbol | ETNK1 |
| name | ethanolamine kinase 1 |
| refseq_nuc | NM_018638.5 |
| refseq_prot | NP_061108.3 |
| ensembl_nuc | ENST00000266517.9 |
| ensembl_prot | ENSP00000266517.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 22625171 |
| end | 22690665 |
| strand | + |
| ver | v1.2 |
| region | chr12:22625171-22690665 |
| region5000 | chr12:22620171-22695665 |
| regionname0 | ETNK1_chr12_22625171_22690665 |
| regionname5000 | ETNK1_chr12_22620171_22695665 |
| 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 | 363 | 310 | 96 | 58 | 116 | 7 | 31 | 94 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0002 | 0/0 | 363 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0003 | 0/0 | 363 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0004 | 0/0 | 363 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| 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 | 1092 | 218 | 79 | 49 | 59 | 5 | 24 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0002 | 0/0 | 1092 | 82 | 9 | 7 | 57 | 2 | 7 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0003 | 0/0 | 1092 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0004 | 0/0 | 1092 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0005 | 0/0 | 1092 | 3 | 2 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0006 | 0/0 | 1092 | 3 | 0 | 0 | 0 | 1 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0007 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0008 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0009 | 0/0 | 1092 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| c0010 | 0/0 | 1092 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| 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 | 0/0 | 5972 | 51 | 2 | 4 | 37 | 1 | 7 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0002 | 1/0 | 5972 | 50 | 18 | 15 | 4 | 4 | 8 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0003 | 0/1 | 5970 | 41 | 5 | 15 | 15 | 1 | 4 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0004 | 0/0 | 5971 | 19 | 0 | 5 | 6 | 1 | 7 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0005 | 0/0 | 5973 | 15 | 1 | 2 | 11 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0006 | 0/0 | 5972 | 11 | 0 | 0 | 10 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0007 | 0/0 | 5973 | 10 | 7 | 0 | 2 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0008 | 0/0 | 5972 | 9 | 0 | 0 | 9 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0009 | 0/0 | 5970 | 8 | 8 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0010 | 0/0 | 5971 | 7 | 0 | 4 | 1 | 0 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0011 | 0/0 | 5974 | 7 | 5 | 1 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0012 | 0/0 | 5975 | 7 | 6 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0013 | 0/0 | 5973 | 6 | 4 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0014 | 0/0 | 5971 | 6 | 6 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0015 | 0/0 | 5971 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0016 | 0/0 | 5971 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0017 | 0/0 | 5973 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0018 | 0/0 | 5971 | 3 | 1 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0019 | 0/0 | 5971 | 3 | 2 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0020 | 0/0 | 5972 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0021 | 0/0 | 5972 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0022 | 0/0 | 5972 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0023 | 0/0 | 5968 | 2 | 1 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0024 | 0/0 | 5972 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0025 | 0/0 | 5971 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0026 | 0/0 | 5974 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0027 | 0/0 | 5972 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0028 | 0/0 | 5972 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0029 | 0/0 | 5971 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0030 | 0/0 | 5972 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0031 | 0/0 | 5973 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0032 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0033 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0034 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0035 | 0/0 | 5972 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0036 | 0/0 | 5972 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0037 | 0/0 | 5972 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0038 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0039 | 0/0 | 5972 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0040 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0041 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0042 | 0/0 | 5972 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0043 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0044 | 0/0 | 5972 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0045 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0046 | 0/0 | 5972 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0047 | 0/0 | 5973 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0048 | 0/0 | 5973 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0049 | 0/0 | 5973 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0050 | 0/0 | 5973 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0051 | 0/0 | 5973 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0052 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0053 | 0/0 | 5972 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0054 | 0/0 | 5974 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0055 | 0/0 | 5971 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0056 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0057 | 0/0 | 5972 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| t0058 | 0/0 | 5972 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| 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 | 7 | 7 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0004 | 0/0 | 5 | 0 | 1 | 1 | 2 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0007 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0010 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0012 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| 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 | 1092 | 218 | 79 | 49 | 59 | 5 | 24 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002 | 0/0 | 1092 | 82 | 9 | 7 | 57 | 2 | 7 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0003 | 0/0 | 1092 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0005 | 0/0 | 1092 | 3 | 2 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0007 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0008 | 0/0 | 1092 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0009 | 0/0 | 1092 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0002c0004 | 0/0 | 1092 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0003c0006 | 0/0 | 1092 | 3 | 0 | 0 | 0 | 1 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0004c0010 | 0/0 | 1092 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7063 | 11 | 2 | 0 | 9 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0002 | 1/0 | 7063 | 45 | 14 | 15 | 4 | 3 | 8 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0003 | 0/1 | 7061 | 40 | 4 | 15 | 15 | 1 | 4 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0004 | 0/0 | 7062 | 18 | 0 | 5 | 6 | 1 | 6 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0005 | 0/0 | 7064 | 3 | 1 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0007 | 0/0 | 7064 | 9 | 6 | 0 | 2 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0008 | 0/0 | 7063 | 9 | 0 | 0 | 9 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0009 | 0/0 | 7061 | 8 | 8 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0010 | 0/0 | 7062 | 7 | 0 | 4 | 1 | 0 | 2 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0011 | 0/0 | 7065 | 4 | 2 | 1 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0012 | 0/0 | 7066 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0013 | 0/0 | 7064 | 6 | 4 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0014 | 0/0 | 7062 | 6 | 6 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0015 | 0/0 | 7062 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0017 | 0/0 | 7064 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0018 | 0/0 | 7062 | 3 | 1 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0019 | 0/0 | 7062 | 3 | 2 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0020 | 0/0 | 7063 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0022 | 0/0 | 7063 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0023 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0024 | 0/0 | 7063 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0025 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0027 | 0/0 | 7063 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0028 | 0/0 | 7063 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0029 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0032 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0034 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0035 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0036 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0037 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0038 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0040 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0041 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0042 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0043 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0044 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0045 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0046 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0047 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0049 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0050 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0053 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0054 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0055 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0056 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0001t0057 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0001 | 0/0 | 7063 | 37 | 0 | 4 | 26 | 1 | 6 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0002 | 0/0 | 7063 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0005 | 0/0 | 7064 | 10 | 0 | 2 | 7 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0006 | 0/0 | 7063 | 11 | 0 | 0 | 10 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0012 | 0/0 | 7066 | 5 | 5 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0016 | 0/0 | 7062 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0021 | 0/0 | 7063 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0026 | 0/0 | 7065 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0030 | 0/0 | 7063 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0031 | 0/0 | 7064 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0039 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0002t0051 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0003t0007 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0003t0011 | 0/0 | 7065 | 3 | 3 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0005t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0005t0048 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0005t0052 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0007t0003 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0008t0033 | 0/0 | 7060 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0001c0009t0023 | 0/0 | 7059 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0002c0004t0001 | 0/0 | 7063 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0002c0004t0005 | 0/0 | 7064 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0003c0006t0001 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0003c0006t0002 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0003c0006t0058 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| a0004c0010t0004 | 0/0 | 7062 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | copy fasta | chr12 | 22620171 | 22695665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 1 | 1 | 2 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0021 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0234 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0007 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0011g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0015g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0015g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0015g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0017g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0017g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0017g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0018g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0018g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0019g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0019g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0020g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0020g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0020g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0022g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0022g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0023g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0024g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0024g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0025g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0025g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0027g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0027g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0028g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0028g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0029g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0029g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0032g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0034g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0035g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0036g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0037g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0038g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0040g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0041g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0042g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0043g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0044g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0045g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0046g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0047g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0049g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0050g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0053g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0054g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0055g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0056g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0001t0057g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0012g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0016g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0021g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0021g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0021g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0026g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0026g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0030g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0030g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0031g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0031g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0039g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0002t0051g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0003t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0003t0011g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0003t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0005t0012g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0005t0048g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0005t0052g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0007t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0008t0033g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0001c0009t0023g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0002c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0002c0004t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0002c0004t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0002c0004t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0003c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0003c0006t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0003c0006t0058g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| a0004c0010t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0006 | t0002 | g0119 | EUR | GBR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0212 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0151 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0007 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00323 | hp2 | a0001 | c0002 | t0006 | g0066 | EUR | FIN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0009 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00408 | hp2 | a0001 | c0002 | t0006 | g0063 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00423 | hp1 | a0001 | c0002 | t0006 | g0002 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00423 | hp2 | a0001 | c0001 | t0024 | g0248 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00544 | hp1 | a0001 | c0001 | t0013 | g0191 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00558 | hp2 | a0001 | c0001 | t0015 | g0031 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00621 | hp2 | a0001 | c0002 | t0006 | g0065 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0054 | EAS | CHS | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00741 | hp1 | a0001 | c0001 | t0050 | g0217 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01071 | hp1 | a0001 | c0001 | t0044 | g0027 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01109 | hp1 | a0001 | c0001 | t0042 | g0230 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0006 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01168 | hp1 | a0001 | c0001 | t0018 | g0039 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01169 | hp2 | a0001 | c0001 | t0018 | g0040 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01175 | hp2 | a0001 | c0001 | t0035 | g0251 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0012 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01243 | hp2 | a0001 | c0005 | t0048 | g0020 | AMR | PUR | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0252 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01358 | hp2 | a0001 | c0009 | t0023 | g0152 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0034 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01884 | hp2 | a0001 | c0003 | t0011 | g0017 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0240 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0105 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01934 | hp2 | a0001 | c0001 | t0010 | g0237 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01943 | hp1 | a0001 | c0001 | t0036 | g0106 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0160 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01952 | hp2 | a0001 | c0002 | t0051 | g0010 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0082 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0202 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02027 | hp2 | a0001 | c0002 | t0031 | g0015 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02129 | hp2 | a0001 | c0002 | t0016 | g0016 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02132 | hp1 | a0001 | c0002 | t0006 | g0057 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02135 | hp2 | a0001 | c0002 | t0006 | g0002 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0098 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02145 | hp2 | a0001 | c0001 | t0047 | g0052 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0146 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02258 | hp2 | a0001 | c0005 | t0052 | g0120 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02273 | hp2 | a0001 | c0001 | t0010 | g0013 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02280 | hp2 | a0001 | c0001 | t0017 | g0241 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02293 | hp1 | a0001 | c0001 | t0053 | g0028 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02293 | hp2 | a0001 | c0001 | t0010 | g0170 | AMR | PEL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02451 | hp1 | a0001 | c0003 | t0007 | g0112 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02523 | hp2 | a0001 | c0001 | t0015 | g0246 | EAS | KHV | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02572 | hp1 | a0001 | c0001 | t0025 | g0033 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02572 | hp2 | a0001 | c0001 | t0020 | g0044 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02602 | hp1 | a0001 | c0001 | t0049 | g0222 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02602 | hp2 | a0001 | c0001 | t0057 | g0123 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02615 | hp1 | a0001 | c0001 | t0028 | g0046 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02615 | hp2 | a0001 | c0001 | t0043 | g0233 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02622 | hp1 | a0001 | c0001 | t0029 | g0195 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02622 | hp2 | a0001 | c0001 | t0027 | g0081 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0137 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02647 | hp2 | a0001 | c0001 | t0041 | g0012 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02698 | hp2 | a0001 | c0001 | t0019 | g0229 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02717 | hp2 | a0001 | c0001 | t0014 | g0136 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02809 | hp1 | a0001 | c0001 | t0029 | g0196 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02818 | hp1 | a0001 | c0005 | t0012 | g0003 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02818 | hp2 | a0001 | c0001 | t0014 | g0001 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02886 | hp1 | a0001 | c0001 | t0045 | g0035 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0090 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02895 | hp2 | a0001 | c0001 | t0028 | g0047 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02896 | hp2 | a0001 | c0002 | t0012 | g0019 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02897 | hp2 | a0001 | c0001 | t0019 | g0030 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0199 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02965 | hp1 | a0001 | c0001 | t0022 | g0145 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0051 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02976 | hp1 | a0001 | c0001 | t0017 | g0239 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0138 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03017 | hp2 | a0001 | c0001 | t0010 | g0149 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03098 | hp1 | a0001 | c0001 | t0014 | g0143 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0140 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03130 | hp1 | a0001 | c0001 | t0022 | g0001 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03130 | hp2 | a0001 | c0001 | t0020 | g0041 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03139 | hp1 | a0001 | c0002 | t0012 | g0003 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0198 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03195 | hp1 | a0001 | c0001 | t0023 | g0037 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03195 | hp2 | a0001 | c0008 | t0033 | g0171 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03209 | hp1 | a0001 | c0007 | t0003 | g0165 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03209 | hp2 | a0001 | c0001 | t0040 | g0049 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03225 | hp1 | a0001 | c0001 | t0038 | g0126 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03225 | hp2 | a0001 | c0001 | t0055 | g0142 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03453 | hp2 | a0001 | c0001 | t0011 | g0050 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0043 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03516 | hp1 | a0001 | c0001 | t0054 | g0201 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03540 | hp2 | a0001 | c0001 | t0020 | g0042 | AFR | GWD | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03579 | hp1 | a0001 | c0001 | t0027 | g0012 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0139 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03654 | hp1 | a0003 | c0006 | t0001 | g0086 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03688 | hp1 | a0001 | c0001 | t0007 | g0026 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03688 | hp2 | a0001 | c0002 | t0005 | g0085 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0238 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03834 | hp2 | a0003 | c0006 | t0058 | g0114 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0249 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03942 | hp1 | a0004 | c0010 | t0004 | g0247 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0219 | SAS | BEB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0147 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0110 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0101 | SAS | STU | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0197 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18906 | hp1 | a0001 | c0001 | t0009 | g0144 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18942 | hp1 | a0001 | c0002 | t0016 | g0045 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18942 | hp2 | a0001 | c0002 | t0030 | g0015 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18946 | hp1 | a0001 | c0002 | t0039 | g0130 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18946 | hp2 | a0001 | c0001 | t0015 | g0242 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18949 | hp1 | a0001 | c0002 | t0005 | g0087 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18949 | hp2 | a0001 | c0002 | t0030 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18951 | hp2 | a0001 | c0001 | t0046 | g0102 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18954 | hp1 | a0002 | c0004 | t0001 | g0062 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18959 | hp1 | a0001 | c0002 | t0021 | g0099 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18960 | hp2 | a0001 | c0001 | t0008 | g0187 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18961 | hp1 | a0001 | c0001 | t0008 | g0190 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18964 | hp2 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18965 | hp2 | a0001 | c0002 | t0026 | g0205 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18967 | hp1 | a0001 | c0001 | t0010 | g0159 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18978 | hp1 | a0001 | c0002 | t0005 | g0075 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18978 | hp2 | a0001 | c0001 | t0015 | g0031 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18983 | hp2 | a0001 | c0002 | t0006 | g0018 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18995 | hp2 | a0001 | c0001 | t0008 | g0025 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18998 | hp1 | a0001 | c0002 | t0005 | g0074 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA18998 | hp2 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19004 | hp1 | a0001 | c0001 | t0037 | g0207 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19004 | hp2 | a0001 | c0002 | t0026 | g0076 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19006 | hp1 | a0001 | c0001 | t0005 | g0134 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19007 | hp1 | a0001 | c0002 | t0005 | g0088 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19007 | hp2 | a0002 | c0004 | t0005 | g0061 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19009 | hp1 | a0001 | c0002 | t0006 | g0018 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19011 | hp1 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19012 | hp1 | a0001 | c0001 | t0024 | g0255 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19030 | hp2 | a0001 | c0002 | t0012 | g0003 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19043 | hp1 | a0001 | c0001 | t0034 | g0135 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19058 | hp1 | a0001 | c0002 | t0006 | g0002 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19063 | hp1 | a0001 | c0002 | t0021 | g0070 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19065 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19068 | hp2 | a0001 | c0002 | t0021 | g0006 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19070 | hp1 | a0001 | c0001 | t0008 | g0189 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19074 | hp2 | a0001 | c0002 | t0016 | g0048 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19075 | hp1 | a0001 | c0001 | t0008 | g0025 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19075 | hp2 | a0002 | c0004 | t0005 | g0009 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19076 | hp2 | a0001 | c0002 | t0016 | g0058 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19078 | hp1 | a0001 | c0002 | t0031 | g0064 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19084 | hp1 | a0001 | c0001 | t0008 | g0192 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19084 | hp2 | a0001 | c0002 | t0005 | g0117 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19085 | hp2 | a0001 | c0002 | t0005 | g0079 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0103 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19091 | hp1 | a0001 | c0001 | t0013 | g0194 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19240 | hp1 | a0001 | c0001 | t0022 | g0001 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA19240 | hp2 | a0001 | c0002 | t0012 | g0003 | AFR | YRI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | ASW | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20129 | hp2 | a0001 | c0001 | t0032 | g0257 | AFR | ASW | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0109 | EUR | TSI | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | GIH | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0245 | SAS | GIH | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0203 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | CLM | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02109 | hp1 | a0001 | c0001 | t0056 | g0127 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0141 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | MSL | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| HG06807 | hp2 | a0001 | c0003 | t0011 | g0113 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20300 | hp1 | a0001 | c0003 | t0011 | g0017 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0200 | AFR | USA | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| NA21309 | hp2 | a0001 | c0002 | t0012 | g0003 | AFR | LWK | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0234 | REF | REF | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0021 | REF | REF | ETNK1_chr12_22620171_22695665 | ETNK1 | chr12 | 22620171 | 22695665 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22643805
|
G | A | 1 | a0002 | 4 | NA18954.hp1 NA19007.hp2 NA19065.hp1 others(1): Show |
missense_variant | MODERATE | c.199G>A | p.Val67Met | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/8 | 459/7063 | 199/1092 | 67/363 | chr12 | 22643805 | ||
| chr12:22661089
|
A | G | 1 | a0003 | 3 | HG00099.hp1 HG03654.hp1 HG03834.hp2 |
missense_variant | MODERATE | c.584A>G | p.Gln195Arg | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/8 | 844/7063 | 584/1092 | 195/363 | chr12 | 22661089 | ||
| chr12:22673582
|
A | T | 1 | a0004 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.867A>T | p.Lys289Asn | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/8 | 1127/7063 | 867/1092 | 289/363 | chr12 | 22673582 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22625439
|
T | C | 1 | a0001c0003 | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.9T>C | p.Asn3Asn | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/8 | 269/7063 | 9/1092 | 3/363 | chr12 | 22625439 | ||
| chr12:22625574
|
G | A | 3 | a0001c0005a0001c0007a0001c0008 | 5 | HG01243.hp2 HG02258.hp2 HG02818.hp1 others(2): Show |
synonymous_variant | LOW | c.144G>A | p.Glu48Glu | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/8 | 404/7063 | 144/1092 | 48/363 | chr12 | 22625574 | ||
| chr12:22661102
|
A | G | 3 | a0001c0002a0001c0005a0002c0004 | 89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
synonymous_variant | LOW | c.597A>G | p.Glu199Glu | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/8 | 857/7063 | 597/1092 | 199/363 | chr12 | 22661102 | ||
| chr12:22661105
|
G | A | 1 | a0001c0007 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.600G>A | p.Glu200Glu | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/8 | 860/7063 | 600/1092 | 200/363 | chr12 | 22661105 | ||
| chr12:22684909
|
C | T | 1 | a0001c0009 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.1047C>T | p.Tyr349Tyr | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1307/7063 | 1047/1092 | 349/363 | chr12 | 22684909 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22625223
|
C | T | 1 | a0003c0006t0058 | 1 | HG03834.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-208C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/8 | chr12 | 22625223 | ||||||
| chr12:22685032
|
T | G | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 78 | chr12 | 22685032 | |||||
| chr12:22685291
|
C | T | 1 | a0001c0001t0057 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 337 | chr12 | 22685291 | |||||
| chr12:22685327
|
A | C | 1 | a0001c0001t0056 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 373 | chr12 | 22685327 | |||||
| chr12:22685751
|
TATCA | T | 6 | a0001c0001t0003a0001c0001t0010a0001c0001t0023others(3): Show | 51 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*802delTCAA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 799 | INFO_REALIGN_3_PRIME | chr12 | 22685751 | ||||
| chr12:22685822
|
T | G | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 868 | chr12 | 22685822 | |||||
| chr12:22686584
|
A | T | 4 | a0001c0001t0009a0001c0001t0014a0001c0001t0022others(1): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1630A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1630 | chr12 | 22686584 | |||||
| chr12:22686647
|
A | G | 8 | a0001c0001t0008a0001c0001t0013a0001c0001t0029others(5): Show | 34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1693A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1693 | chr12 | 22686647 | |||||
| chr12:22686751
|
T | C | 2 | a0001c0001t0015a0001c0001t0024 | 6 | HG00423.hp2 HG00558.hp2 HG02523.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1797T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1797 | chr12 | 22686751 | |||||
| chr12:22686802
|
G | A | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0009others(17): Show | 104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1848G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1848 | chr12 | 22686802 | |||||
| chr12:22686819
|
A | G | 1 | a0001c0001t0053 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1865A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1865 | chr12 | 22686819 | |||||
| chr12:22686851
|
A | AT | 17 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(14): Show | 65 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1925dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1926 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | ||||
| chr12:22686851
|
A | ATT | 9 | a0001c0001t0003a0001c0001t0011a0001c0001t0024others(6): Show | 55 | HG00280.hp2 HG00423.hp2 HG00733.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1924_*1925dupTT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1926 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | ||||
| chr12:22686851
|
A | ATTT | 5 | a0001c0001t0010a0001c0001t0012a0001c0002t0012others(2): Show | 15 | HG01243.hp1 HG01934.hp2 HG01952.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1923_*1925dupTTT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1926 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | ||||
| chr12:22686851
|
AT | A | 7 | a0001c0001t0014a0001c0001t0018a0001c0001t0019others(4): Show | 21 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1925delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1925 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | ||||
| chr12:22686851
|
ATT | A | 1 | a0001c0001t0009 | 8 | HG01891.hp2 HG02257.hp1 HG02922.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1924_*1925delTT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1924 | INFO_REALIGN_3_PRIME | chr12 | 22686851 | ||||
| chr12:22686909
|
A | G | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1955A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 1955 | chr12 | 22686909 | |||||
| chr12:22686966
|
T | G | 1 | a0001c0001t0036 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2012T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2012 | chr12 | 22686966 | |||||
| chr12:22686990
|
G | C | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2036G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2036 | chr12 | 22686990 | |||||
| chr12:22687042
|
A | G | 1 | a0001c0001t0046 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2088 | chr12 | 22687042 | |||||
| chr12:22687085
|
C | T | 1 | a0001c0001t0045 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2131C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2131 | chr12 | 22687085 | |||||
| chr12:22687158
|
A | G | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0024others(2): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2204A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2204 | chr12 | 22687158 | |||||
| chr12:22687201
|
A | G | 1 | a0001c0001t0044 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2247A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2247 | chr12 | 22687201 | |||||
| chr12:22687211
|
T | C | 2 | a0001c0001t0018a0001c0001t0020 | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2257T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2257 | chr12 | 22687211 | |||||
| chr12:22687324
|
A | C | 1 | a0001c0002t0021 | 3 | NA18959.hp1 NA19063.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2370A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2370 | chr12 | 22687324 | |||||
| chr12:22687494
|
A | G | 1 | a0001c0002t0051 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2540A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2540 | chr12 | 22687494 | |||||
| chr12:22687861
|
A | G | 1 | a0001c0001t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2907A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 2907 | chr12 | 22687861 | |||||
| chr12:22688064
|
C | T | 2 | a0001c0001t0043a0001c0001t0050 | 2 | HG00741.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3110C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3110 | chr12 | 22688064 | |||||
| chr12:22688065
|
G | A | 1 | a0001c0001t0037 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3111G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3111 | chr12 | 22688065 | |||||
| chr12:22688158
|
A | C | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0024others(2): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3204A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3204 | chr12 | 22688158 | |||||
| chr12:22688173
|
A | G | 1 | a0001c0001t0042 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3219A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3219 | chr12 | 22688173 | |||||
| chr12:22688370
|
C | T | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0024others(2): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3416C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3416 | chr12 | 22688370 | |||||
| chr12:22688412
|
T | G | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3458T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3458 | chr12 | 22688412 | |||||
| chr12:22688426
|
A | C | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0024others(2): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3472A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3472 | chr12 | 22688426 | |||||
| chr12:22688553
|
A | T | 4 | a0001c0001t0009a0001c0001t0014a0001c0001t0022others(1): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3599A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3599 | chr12 | 22688553 | |||||
| chr12:22688589
|
A | G | 1 | a0001c0001t0049 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3635A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3635 | chr12 | 22688589 | |||||
| chr12:22688620
|
A | G | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3666A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3666 | chr12 | 22688620 | |||||
| chr12:22688730
|
A | T | 1 | a0001c0001t0032 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3776A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3776 | chr12 | 22688730 | |||||
| chr12:22688754
|
G | A | 1 | a0001c0001t0038 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3800G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3800 | chr12 | 22688754 | |||||
| chr12:22688821
|
G | A | 1 | a0001c0002t0030 | 2 | NA18942.hp2 NA18949.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3867G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 3867 | chr12 | 22688821 | |||||
| chr12:22689043
|
A | G | 3 | a0001c0001t0027a0001c0001t0041a0001c0005t0048 | 4 | HG01243.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4089A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4089 | chr12 | 22689043 | |||||
| chr12:22689262
|
CTA | C | 5 | a0001c0001t0004a0001c0001t0015a0001c0001t0024others(2): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4310_*4311delAT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4310 | INFO_REALIGN_3_PRIME | chr12 | 22689262 | ||||
| chr12:22689340
|
A | G | 2 | a0001c0001t0040a0001c0001t0047 | 2 | HG02145.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4386A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4386 | chr12 | 22689340 | |||||
| chr12:22689488
|
A | G | 1 | a0001c0001t0037 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4534A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4534 | chr12 | 22689488 | |||||
| chr12:22689625
|
G | A | 1 | a0001c0002t0039 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4671G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4671 | chr12 | 22689625 | |||||
| chr12:22689793
|
G | A | 1 | a0001c0001t0028 | 2 | HG02615.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4839G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4839 | chr12 | 22689793 | |||||
| chr12:22689844
|
A | G | 7 | a0001c0001t0004a0001c0001t0015a0001c0001t0024others(4): Show | 29 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4890A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 4890 | chr12 | 22689844 | |||||
| chr12:22690077
|
A | G | 1 | a0001c0001t0041 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5123A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5123 | chr12 | 22690077 | |||||
| chr12:22690128
|
C | T | 1 | a0001c0005t0052 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5174C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5174 | chr12 | 22690128 | |||||
| chr12:22690273
|
A | C | 19 | a0001c0001t0001a0001c0001t0005a0001c0001t0027others(16): Show | 97 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*5319A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5319 | chr12 | 22690273 | |||||
| chr12:22690573
|
C | T | 1 | a0001c0001t0055 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5619C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 8/8 | 5619 | chr12 | 22690573 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:22625601
|
T | C | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.156+15T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625601 | ||||||
| chr12:22625651
|
C | G | 2 | a0001c0001t0007g0256a0001c0001t0032g0257 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.156+65C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625651 | ||||||
| chr12:22625653
|
A | G | 1 | a0001c0001t0024g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.156+67A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625653 | ||||||
| chr12:22625699
|
C | T | 24 | a0001c0001t0002g0030a0001c0001t0004g0032a0001c0001t0004g0238others(21): Show | 26 | HG00423.hp2 HG00558.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.156+113C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625699 | ||||||
| chr12:22625767
|
C | G | 44 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0004others(41): Show | 49 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.156+181C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625767 | ||||||
| chr12:22625905
|
A | G | 16 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(13): Show | 17 | HG00544.hp1 HG02622.hp1 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.156+319A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22625905 | ||||||
| chr12:22626078
|
T | A | 1 | a0001c0001t0004g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.156+492T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626078 | ||||||
| chr12:22626226
|
CTG | C | 17 | a0001c0001t0004g0032a0001c0001t0004g0238a0001c0001t0004g0243others(14): Show | 19 | HG00423.hp2 HG00558.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.156+642_156+643del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22626226 | |||||
| chr12:22626257
|
A | G | 3 | a0001c0001t0017g0239a0001c0001t0017g0240a0001c0001t0017g0241 | 3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.156+671A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626257 | ||||||
| chr12:22626296
|
G | A | 1 | a0001c0001t0045g0035 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.156+710G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626296 | ||||||
| chr12:22626297
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+711G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626297 | ||||||
| chr12:22626400
|
C | A | 3 | a0001c0001t0017g0239a0001c0001t0017g0240a0001c0001t0017g0241 | 3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.156+814C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626400 | ||||||
| chr12:22626426
|
CA | C | 86 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(83): Show | 101 | HG00280.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.156+849delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22626426 | |||||
| chr12:22626732
|
G | T | 1 | a0001c0001t0003g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.156+1146G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626732 | ||||||
| chr12:22626892
|
T | C | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+1306T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22626892 | ||||||
| chr12:22627150
|
A | AT | 45 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(42): Show | 52 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.156+1574dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22627150 | |||||
| chr12:22627150
|
A | ATTT | 13 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(10): Show | 15 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.156+1572_156+1574d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22627150 | |||||
| chr12:22627160
|
T | TTA | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.156+1574_156+1575i others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22627160 | ||||||
| chr12:22627174
|
G | A | 268 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(265): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.156+1588G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22627174 | ||||||
| chr12:22627189
|
G | A | 1 | a0001c0001t0007g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.156+1603G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22627189 | ||||||
| chr12:22628193
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+2607G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628193 | ||||||
| chr12:22628596
|
G | C | 1 | a0001c0001t0010g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.156+3010G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628596 | ||||||
| chr12:22628614
|
C | T | 17 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(14): Show | 18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.156+3028C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628614 | ||||||
| chr12:22628746
|
A | G | 9 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0002g0121others(6): Show | 12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+3160A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628746 | ||||||
| chr12:22628811
|
T | A | 8 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.156+3225T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628811 | ||||||
| chr12:22628887
|
A | G | 1 | a0001c0001t0009g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.156+3301A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628887 | ||||||
| chr12:22628984
|
A | G | 1 | a0003c0006t0002g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.156+3398A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22628984 | ||||||
| chr12:22629079
|
A | G | 1 | a0001c0001t0054g0201 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.156+3493A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629079 | ||||||
| chr12:22629088
|
T | A | 2 | a0001c0002t0002g0019a0001c0002t0012g0019 | 2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.156+3502T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629088 | ||||||
| chr12:22629290
|
A | G | 1 | a0001c0002t0002g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.156+3704A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629290 | ||||||
| chr12:22629757
|
C | T | 1 | a0001c0002t0006g0018 | 2 | NA18983.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.156+4171C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629757 | ||||||
| chr12:22629786
|
A | G | 2 | a0001c0001t0032g0257a0001c0001t0034g0135 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.156+4200A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629786 | ||||||
| chr12:22629889
|
C | T | 1 | a0001c0001t0007g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.156+4303C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629889 | ||||||
| chr12:22629928
|
T | A | 69 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(66): Show | 82 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.156+4342T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22629928 | ||||||
| chr12:22630106
|
A | G | 1 | a0001c0002t0002g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.156+4520A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630106 | ||||||
| chr12:22630118
|
T | C | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.156+4532T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630118 | ||||||
| chr12:22630149
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+4563T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630149 | ||||||
| chr12:22630249
|
C | T | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.156+4663C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630249 | ||||||
| chr12:22630255
|
T | G | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.156+4669T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630255 | ||||||
| chr12:22630265
|
A | G | 1 | a0001c0001t0003g0177 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.156+4679A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630265 | ||||||
| chr12:22630474
|
A | C | 1 | a0001c0001t0004g0254 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.156+4888A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630474 | ||||||
| chr12:22630504
|
A | C | 1 | a0001c0002t0001g0118 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.156+4918A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630504 | ||||||
| chr12:22630548
|
G | GCTTA | 3 | a0001c0002t0001g0115a0001c0002t0001g0116a0001c0002t0005g0117 | 3 | NA18945.hp1 NA18987.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.156+4965_156+4968d others(6): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22630548 | |||||
| chr12:22630629
|
T | C | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+5043T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630629 | ||||||
| chr12:22630720
|
C | T | 1 | a0001c0002t0005g0117 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.156+5134C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630720 | ||||||
| chr12:22630757
|
T | G | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+5171T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630757 | ||||||
| chr12:22630759
|
C | T | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+5173C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630759 | ||||||
| chr12:22630811
|
A | G | 73 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(70): Show | 86 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.156+5225A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630811 | ||||||
| chr12:22630881
|
G | T | 1 | a0003c0006t0058g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.156+5295G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630881 | ||||||
| chr12:22630937
|
A | G | 3 | a0001c0003t0007g0112a0001c0003t0011g0017a0001c0003t0011g0113 | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+5351A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630937 | ||||||
| chr12:22630977
|
G | A | 1 | a0001c0001t0003g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.156+5391G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630977 | ||||||
| chr12:22630989
|
G | A | 1 | a0001c0002t0016g0045 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.156+5403G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22630989 | ||||||
| chr12:22631177
|
C | CT | 31 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(28): Show | 38 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.156+5605dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22631177 | |||||
| chr12:22631335
|
T | C | 95 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(92): Show | 113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.156+5749T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631335 | ||||||
| chr12:22631343
|
T | C | 2 | a0001c0001t0028g0046a0001c0001t0028g0047 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.156+5757T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631343 | ||||||
| chr12:22631499
|
C | T | 1 | a0001c0002t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.156+5913C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631499 | ||||||
| chr12:22631629
|
G | A | 1 | a0001c0002t0016g0048 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.156+6043G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631629 | ||||||
| chr12:22631660
|
G | A | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.156+6074G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631660 | ||||||
| chr12:22631785
|
G | A | 1 | a0001c0001t0040g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.156+6199G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631785 | ||||||
| chr12:22631954
|
A | G | 1 | a0001c0001t0002g0232 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.156+6368A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22631954 | ||||||
| chr12:22632014
|
A | G | 1 | a0001c0001t0013g0200 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156+6428A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632014 | ||||||
| chr12:22632078
|
A | AT | 152 | a0001c0001t0001g0083a0001c0001t0001g0209a0001c0001t0001g0210others(149): Show | 176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.156+6504dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632078 | |||||
| chr12:22632078
|
AT | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(5): Show | 10 | HG03453.hp2 NA18965.hp1 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+6504delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632078 | |||||
| chr12:22632168
|
G | A | 68 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(65): Show | 81 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.156+6582G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632168 | ||||||
| chr12:22632217
|
A | T | 1 | a0001c0001t0002g0231 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.156+6631A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632217 | ||||||
| chr12:22632353
|
A | G | 1 | a0001c0001t0005g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.156+6767A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632353 | ||||||
| chr12:22632382
|
C | G | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.156+6796C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632382 | ||||||
| chr12:22632482
|
C | G | 1 | a0001c0001t0002g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.156+6896C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632482 | ||||||
| chr12:22632515
|
C | CT | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.156+6939dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632515 | |||||
| chr12:22632593
|
T | TTGTACTC others(18): Show |
1 | a0001c0001t0010g0149 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.156+7026_156+7027i others(27): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22632593 | |||||
| chr12:22632613
|
G | C | 73 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(70): Show | 86 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.156+7027G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632613 | ||||||
| chr12:22632701
|
C | T | 28 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(25): Show | 34 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.156+7115C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632701 | ||||||
| chr12:22632733
|
T | C | 29 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(26): Show | 35 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.156+7147T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632733 | ||||||
| chr12:22632782
|
G | T | 6 | a0001c0001t0009g0001a0001c0001t0009g0144a0001c0001t0014g0001others(3): Show | 10 | HG01891.hp2 HG02818.hp2 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+7196G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632782 | ||||||
| chr12:22632837
|
G | A | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.156+7251G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632837 | ||||||
| chr12:22632952
|
A | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(11): Show | 16 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+7366A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22632952 | ||||||
| chr12:22633120
|
A | G | 2 | a0001c0001t0003g0024a0001c0001t0003g0176 | 3 | HG02055.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.156+7534A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633120 | ||||||
| chr12:22633149
|
T | G | 14 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(11): Show | 16 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.156+7563T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633149 | ||||||
| chr12:22633174
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.156+7588C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633174 | ||||||
| chr12:22633547
|
A | G | 1 | a0003c0006t0002g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.156+7961A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633547 | ||||||
| chr12:22633582
|
A | G | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.156+7996A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633582 | ||||||
| chr12:22633631
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.156+8045A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633631 | ||||||
| chr12:22633775
|
G | A | 1 | a0001c0002t0006g0057 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.156+8189G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633775 | ||||||
| chr12:22633873
|
A | G | 1 | a0001c0001t0042g0230 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.156+8287A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633873 | ||||||
| chr12:22633882
|
A | G | 29 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(26): Show | 35 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.156+8296A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633882 | ||||||
| chr12:22633967
|
G | A | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.156+8381G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22633967 | ||||||
| chr12:22634440
|
A | G | 1 | a0001c0001t0055g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.156+8854A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634440 | ||||||
| chr12:22634557
|
T | C | 1 | a0001c0001t0003g0022 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.156+8971T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634557 | ||||||
| chr12:22634657
|
C | T | 1 | a0001c0001t0019g0229 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.156+9071C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634657 | ||||||
| chr12:22634830
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(9): Show | 14 | HG00621.hp1 HG01884.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.157-8933C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634830 | ||||||
| chr12:22634837
|
A | G | 73 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(70): Show | 86 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.157-8926A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634837 | ||||||
| chr12:22634862
|
T | C | 95 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(92): Show | 113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.157-8901T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634862 | ||||||
| chr12:22634905
|
T | A | 3 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0016g0058 | 3 | HG02129.hp1 NA18951.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.157-8858T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22634905 | ||||||
| chr12:22635145
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.157-8618A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635145 | ||||||
| chr12:22635239
|
T | C | 73 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(70): Show | 86 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.157-8524T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635239 | ||||||
| chr12:22635269
|
T | A | 29 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(26): Show | 35 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.157-8494T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635269 | ||||||
| chr12:22635349
|
G | T | 17 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0029others(14): Show | 18 | HG00639.hp1 HG00738.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-8414G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635349 | ||||||
| chr12:22635432
|
C | T | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-8331C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635432 | ||||||
| chr12:22635446
|
C | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(23): Show | 32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-8317C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635446 | ||||||
| chr12:22635461
|
T | C | 5 | a0001c0002t0005g0009a0002c0004t0001g0009a0002c0004t0001g0062others(2): Show | 5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-8302T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635461 | ||||||
| chr12:22635479
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.157-8284G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635479 | ||||||
| chr12:22635638
|
T | C | 1 | a0001c0001t0005g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.157-8125T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635638 | ||||||
| chr12:22635679
|
G | A | 2 | a0001c0001t0028g0046a0001c0001t0028g0047 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.157-8084G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635679 | ||||||
| chr12:22635839
|
G | T | 26 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(23): Show | 32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-7924G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635839 | ||||||
| chr12:22635878
|
T | A | 10 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(7): Show | 11 | HG00544.hp1 HG02602.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-7885T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22635878 | ||||||
| chr12:22636004
|
C | T | 1 | a0001c0001t0003g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.157-7759C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636004 | ||||||
| chr12:22636130
|
T | C | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-7633T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636130 | ||||||
| chr12:22636140
|
G | T | 1 | a0001c0001t0003g0024 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.157-7623G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636140 | ||||||
| chr12:22636309
|
A | G | 1 | a0001c0001t0007g0128 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.157-7454A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636309 | ||||||
| chr12:22636445
|
A | G | 1 | a0001c0001t0013g0194 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.157-7318A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636445 | ||||||
| chr12:22636522
|
A | G | 2 | a0001c0002t0001g0109a0001c0002t0001g0118 | 2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.157-7241A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636522 | ||||||
| chr12:22636709
|
T | C | 71 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(68): Show | 84 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.157-7054T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636709 | ||||||
| chr12:22636726
|
T | C | 8 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.157-7037T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636726 | ||||||
| chr12:22636815
|
G | A | 23 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(20): Show | 29 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-6948G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636815 | ||||||
| chr12:22636883
|
G | A | 23 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(20): Show | 29 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-6880G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636883 | ||||||
| chr12:22636919
|
A | G | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-6844A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636919 | ||||||
| chr12:22636964
|
G | T | 3 | a0001c0001t0003g0008a0001c0001t0003g0173a0001c0001t0003g0174 | 6 | NA18980.hp1 NA19003.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-6799G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636964 | ||||||
| chr12:22636990
|
G | A | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.157-6773G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22636990 | ||||||
| chr12:22637246
|
C | A | 20 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(17): Show | 25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-6517C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637246 | ||||||
| chr12:22637598
|
A | G | 3 | a0001c0003t0007g0112a0001c0003t0011g0017a0001c0003t0011g0113 | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-6165A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637598 | ||||||
| chr12:22637607
|
C | A | 10 | a0001c0002t0006g0002a0001c0002t0006g0018a0001c0002t0006g0057others(7): Show | 15 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.157-6156C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637607 | ||||||
| chr12:22637698
|
G | A | 1 | a0001c0002t0002g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.157-6065G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637698 | ||||||
| chr12:22637820
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.157-5943T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22637820 | ||||||
| chr12:22637862
|
C | CGA | 42 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(39): Show | 48 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.157-5889_157-5888d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22637862 | |||||
| chr12:22638024
|
A | G | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.157-5739A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638024 | ||||||
| chr12:22638051
|
C | CA | 26 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(23): Show | 32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5703dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22638051 | |||||
| chr12:22638063
|
A | G | 1 | a0001c0002t0001g0221 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.157-5700A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638063 | ||||||
| chr12:22638255
|
G | GT | 7 | a0001c0001t0001g0183a0001c0001t0008g0192a0001c0001t0008g0193others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-5494dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22638255 | |||||
| chr12:22638255
|
GT | G | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.157-5494delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22638255 | |||||
| chr12:22638274
|
C | A | 27 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(24): Show | 32 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5489C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638274 | ||||||
| chr12:22638347
|
G | T | 27 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(24): Show | 32 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5416G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638347 | ||||||
| chr12:22638353
|
A | G | 26 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(23): Show | 32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5410A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638353 | ||||||
| chr12:22638480
|
G | A | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.157-5283G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638480 | ||||||
| chr12:22638513
|
A | C | 43 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0004others(40): Show | 48 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.157-5250A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638513 | ||||||
| chr12:22638613
|
T | A | 26 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(23): Show | 32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-5150T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638613 | ||||||
| chr12:22638755
|
T | C | 1 | a0001c0001t0002g0206 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.157-5008T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22638755 | ||||||
| chr12:22639036
|
A | G | 1 | a0001c0002t0001g0101 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.157-4727A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639036 | ||||||
| chr12:22639072
|
T | C | 3 | a0001c0001t0003g0008a0001c0001t0003g0173a0001c0001t0003g0174 | 6 | NA18980.hp1 NA19003.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-4691T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639072 | ||||||
| chr12:22639178
|
TTTG | T | 17 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(14): Show | 18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-4579_157-4577d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22639178 | |||||
| chr12:22639221
|
A | T | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-4542A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639221 | ||||||
| chr12:22639225
|
T | A | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157-4538T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639225 | ||||||
| chr12:22639327
|
A | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-4436A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639327 | ||||||
| chr12:22639364
|
C | T | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.157-4399C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639364 | ||||||
| chr12:22639447
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.157-4316C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639447 | ||||||
| chr12:22639449
|
G | T | 17 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(14): Show | 18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-4314G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639449 | ||||||
| chr12:22639487
|
G | A | 3 | a0001c0001t0003g0023a0001c0001t0003g0150a0001c0001t0003g0151 | 4 | HG00280.hp2 HG00733.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-4276G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639487 | ||||||
| chr12:22639538
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(6): Show | 11 | HG00621.hp1 HG02559.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-4225A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639538 | ||||||
| chr12:22639581
|
G | A | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.157-4182G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639581 | ||||||
| chr12:22639609
|
G | A | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.157-4154G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639609 | ||||||
| chr12:22639672
|
C | CA | 9 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0002g0121others(6): Show | 12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-4080dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22639672 | |||||
| chr12:22639672
|
CA | C | 25 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(22): Show | 31 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(28): Show |
intron_variant | MODIFIER | c.157-4080delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22639672 | |||||
| chr12:22639695
|
A | G | 3 | a0001c0003t0007g0112a0001c0003t0011g0017a0001c0003t0011g0113 | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-4068A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639695 | ||||||
| chr12:22639759
|
G | A | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-4004G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639759 | ||||||
| chr12:22639836
|
T | C | 1 | a0001c0001t0019g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.157-3927T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639836 | ||||||
| chr12:22639840
|
A | G | 9 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(6): Show | 11 | HG00621.hp1 HG02559.hp2 NA18965.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-3923A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639840 | ||||||
| chr12:22639910
|
C | T | 8 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.157-3853C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639910 | ||||||
| chr12:22639934
|
T | C | 3 | a0001c0001t0010g0149a0001c0001t0010g0237a0001c0009t0023g0152 | 3 | HG01358.hp2 HG01934.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.157-3829T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639934 | ||||||
| chr12:22639958
|
G | C | 1 | a0001c0001t0003g0153 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.157-3805G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22639958 | ||||||
| chr12:22640115
|
G | T | 20 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(17): Show | 25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-3648G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640115 | ||||||
| chr12:22640396
|
CT | C | 15 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0009g0138others(12): Show | 15 | HG01168.hp1 HG01168.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.157-3350delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22640396 | |||||
| chr12:22640620
|
C | T | 1 | a0001c0001t0004g0253 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.157-3143C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640620 | ||||||
| chr12:22640694
|
G | A | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-3069G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640694 | ||||||
| chr12:22640723
|
TAGAG | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-3036_157-3033d others(6): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22640723 | |||||
| chr12:22640742
|
G | A | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-3021G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22640742 | ||||||
| chr12:22641060
|
G | GT | 27 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(24): Show | 33 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.157-2702dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22641060 | |||||
| chr12:22641073
|
C | T | 10 | a0001c0001t0002g0056a0001c0001t0002g0067a0001c0001t0002g0093others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.157-2690C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641073 | ||||||
| chr12:22641256
|
G | A | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-2507G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641256 | ||||||
| chr12:22641289
|
T | C | 67 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(64): Show | 80 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.157-2474T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641289 | ||||||
| chr12:22641293
|
C | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.157-2470C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641293 | ||||||
| chr12:22641453
|
G | A | 3 | a0001c0001t0009g0138a0001c0001t0009g0139a0001c0001t0014g0140 | 3 | HG02976.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.157-2310G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641453 | ||||||
| chr12:22641773
|
C | T | 20 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(17): Show | 25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.157-1990C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641773 | ||||||
| chr12:22641913
|
A | T | 1 | a0001c0001t0003g0172 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.157-1850A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641913 | ||||||
| chr12:22641997
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.157-1766T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22641997 | ||||||
| chr12:22642018
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.157-1745A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642018 | ||||||
| chr12:22642098
|
G | T | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.157-1665G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642098 | ||||||
| chr12:22642303
|
A | G | 1 | a0001c0001t0049g0222 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.157-1460A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642303 | ||||||
| chr12:22642367
|
G | A | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-1396G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642367 | ||||||
| chr12:22642555
|
T | C | 2 | a0001c0002t0001g0068a0001c0002t0016g0048 | 2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.157-1208T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642555 | ||||||
| chr12:22642730
|
T | G | 26 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(23): Show | 32 | HG00621.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.157-1033T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642730 | ||||||
| chr12:22642773
|
T | C | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-990T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642773 | ||||||
| chr12:22642838
|
G | A | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-925G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642838 | ||||||
| chr12:22642949
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.157-814C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22642949 | ||||||
| chr12:22643071
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157-692G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643071 | ||||||
| chr12:22643117
|
A | G | 2 | a0001c0001t0003g0024a0001c0001t0003g0176 | 3 | HG02055.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.157-646A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643117 | ||||||
| chr12:22643353
|
C | G | 1 | a0001c0002t0001g0091 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.157-410C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643353 | ||||||
| chr12:22643381
|
T | C | 17 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(14): Show | 18 | HG00544.hp1 HG02602.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.157-382T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643381 | ||||||
| chr12:22643403
|
A | G | 1 | a0001c0001t0043g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.157-360A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | chr12 | 22643403 | ||||||
| chr12:22643499
|
CAG | C | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-262_157-261del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 22643499 | |||||
| chr12:22644060
|
A | AT | 262 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(259): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.416+38_416+39insT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644060 | ||||||
| chr12:22644150
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.416+128G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644150 | ||||||
| chr12:22644599
|
T | C | 68 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(65): Show | 81 | HG00280.hp2 HG00621.hp1 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.416+577T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644599 | ||||||
| chr12:22644662
|
T | C | 1 | a0001c0002t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.416+640T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644662 | ||||||
| chr12:22644665
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.416+643T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644665 | ||||||
| chr12:22644687
|
T | C | 1 | a0001c0002t0021g0070 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.416+665T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644687 | ||||||
| chr12:22644709
|
A | G | 1 | a0001c0001t0004g0032 | 2 | NA18970.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.416+687A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644709 | ||||||
| chr12:22644729
|
A | G | 20 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0110others(17): Show | 25 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.416+707A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644729 | ||||||
| chr12:22644892
|
G | T | 1 | a0001c0008t0033g0171 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.416+870G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644892 | ||||||
| chr12:22644955
|
C | T | 1 | a0001c0001t0011g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.416+933C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22644955 | ||||||
| chr12:22645011
|
A | G | 1 | a0001c0002t0001g0089 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.416+989A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645011 | ||||||
| chr12:22645110
|
A | G | 2 | a0001c0001t0003g0169a0001c0001t0010g0170 | 2 | HG02293.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.416+1088A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645110 | ||||||
| chr12:22645236
|
G | A | 89 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(86): Show | 107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.416+1214G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645236 | ||||||
| chr12:22645321
|
G | C | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.416+1299G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645321 | ||||||
| chr12:22645378
|
C | A | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.416+1356C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645378 | ||||||
| chr12:22645378
|
C | G | 1 | a0001c0001t0004g0252 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.416+1356C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645378 | ||||||
| chr12:22645511
|
C | T | 2 | a0001c0001t0003g0155a0001c0001t0003g0168 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.416+1489C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645511 | ||||||
| chr12:22645527
|
C | A | 24 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0182others(21): Show | 30 | HG00621.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.416+1505C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645527 | ||||||
| chr12:22645573
|
A | T | 74 | a0001c0001t0001g0083a0001c0001t0012g0012a0001c0001t0027g0012others(71): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.416+1551A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645573 | ||||||
| chr12:22645707
|
T | G | 2 | a0001c0001t0028g0046a0001c0001t0028g0047 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.416+1685T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645707 | ||||||
| chr12:22645738
|
G | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0007g0208others(1): Show | 4 | NA18984.hp2 NA19004.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.416+1716G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645738 | ||||||
| chr12:22645889
|
T | C | 1 | a0001c0001t0007g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.416+1867T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22645889 | ||||||
| chr12:22646012
|
G | A | 1 | a0001c0002t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.416+1990G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646012 | ||||||
| chr12:22646272
|
G | C | 17 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(14): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.416+2250G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646272 | ||||||
| chr12:22646411
|
A | G | 2 | a0001c0002t0005g0087a0001c0002t0005g0088 | 2 | NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.416+2389A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646411 | ||||||
| chr12:22646444
|
G | A | 3 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0001t0010g0159 | 3 | NA18967.hp1 NA18987.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.416+2422G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646444 | ||||||
| chr12:22646663
|
T | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+2641T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646663 | ||||||
| chr12:22646995
|
A | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.416+2973A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22646995 | ||||||
| chr12:22647068
|
C | T | 1 | a0001c0003t0011g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.416+3046C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647068 | ||||||
| chr12:22647155
|
A | T | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.416+3133A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647155 | ||||||
| chr12:22647216
|
A | G | 1 | a0003c0006t0058g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.416+3194A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647216 | ||||||
| chr12:22647300
|
A | G | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.416+3278A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647300 | ||||||
| chr12:22647418
|
A | G | 9 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0002g0121others(6): Show | 12 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.416+3396A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647418 | ||||||
| chr12:22647718
|
C | T | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416+3696C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647718 | ||||||
| chr12:22647828
|
G | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+3806G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647828 | ||||||
| chr12:22647874
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.416+3852G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647874 | ||||||
| chr12:22647992
|
A | G | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.416+3970A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22647992 | ||||||
| chr12:22648012
|
A | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+3990A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648012 | ||||||
| chr12:22648131
|
C | A | 1 | a0001c0001t0008g0192 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.416+4109C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648131 | ||||||
| chr12:22648347
|
A | G | 168 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(165): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.416+4325A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648347 | ||||||
| chr12:22648349
|
A | G | 1 | a0001c0001t0055g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.416+4327A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648349 | ||||||
| chr12:22648567
|
T | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+4545T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648567 | ||||||
| chr12:22648739
|
C | T | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.416+4717C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648739 | ||||||
| chr12:22648818
|
T | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+4796T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648818 | ||||||
| chr12:22648840
|
C | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.416+4818C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22648840 | ||||||
| chr12:22649565
|
C | T | 3 | a0001c0001t0009g0138a0001c0001t0009g0139a0001c0001t0014g0140 | 3 | HG02976.hp2 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.416+5543C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649565 | ||||||
| chr12:22649664
|
C | G | 1 | a0001c0001t0005g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.416+5642C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649664 | ||||||
| chr12:22649682
|
G | C | 17 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(14): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.416+5660G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649682 | ||||||
| chr12:22649721
|
T | C | 2 | a0001c0001t0018g0039a0001c0001t0018g0040 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.416+5699T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649721 | ||||||
| chr12:22649734
|
T | C | 1 | a0001c0001t0010g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.416+5712T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649734 | ||||||
| chr12:22649915
|
G | A | 17 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(14): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.416+5893G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22649915 | ||||||
| chr12:22650176
|
G | A | 2 | a0001c0001t0004g0243a0001c0001t0004g0244 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.416+6154G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650176 | ||||||
| chr12:22650232
|
A | G | 1 | a0001c0001t0008g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.416+6210A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650232 | ||||||
| chr12:22650353
|
T | A | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.416+6331T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650353 | ||||||
| chr12:22650493
|
C | T | 1 | a0001c0001t0003g0236 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.416+6471C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650493 | ||||||
| chr12:22650507
|
A | G | 1 | a0001c0001t0010g0237 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.416+6485A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650507 | ||||||
| chr12:22650733
|
C | G | 1 | a0001c0001t0055g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.416+6711C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650733 | ||||||
| chr12:22650795
|
A | C | 1 | a0001c0001t0002g0227 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.416+6773A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22650795 | ||||||
| chr12:22651259
|
G | T | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.416+7237G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651259 | ||||||
| chr12:22651335
|
G | C | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.416+7313G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651335 | ||||||
| chr12:22651339
|
C | T | 1 | a0001c0001t0011g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.416+7317C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651339 | ||||||
| chr12:22651371
|
T | C | 1 | a0001c0001t0019g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.416+7349T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651371 | ||||||
| chr12:22651379
|
T | G | 28 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(25): Show | 34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.416+7357T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651379 | ||||||
| chr12:22651590
|
A | G | 269 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(266): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.417-7424A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651590 | ||||||
| chr12:22651609
|
T | C | 17 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(14): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-7405T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651609 | ||||||
| chr12:22651630
|
A | C | 3 | a0003c0006t0001g0086a0003c0006t0002g0119a0003c0006t0058g0114 | 3 | HG00099.hp1 HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.417-7384A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651630 | ||||||
| chr12:22651646
|
A | AT | 17 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(14): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-7358dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651646 | |||||
| chr12:22651656
|
T | C | 3 | a0001c0001t0005g0108a0001c0001t0028g0046a0001c0001t0028g0047 | 3 | HG02615.hp1 HG02895.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.417-7358T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651656 | ||||||
| chr12:22651682
|
C | CT | 6 | a0001c0001t0002g0036a0001c0001t0002g0053a0001c0001t0007g0098others(3): Show | 6 | HG02145.hp1 HG02572.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.417-7312dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651682 | |||||
| chr12:22651682
|
CTT | C | 66 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(63): Show | 78 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.417-7313_417-7312d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651682 | |||||
| chr12:22651682
|
CTTT | C | 18 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(15): Show | 22 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.417-7314_417-7312d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22651682 | |||||
| chr12:22651684
|
T | C | 1 | a0001c0001t0017g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.417-7330T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651684 | ||||||
| chr12:22651685
|
T | C | 46 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(43): Show | 53 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.417-7329T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651685 | ||||||
| chr12:22651731
|
C | G | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.417-7283C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651731 | ||||||
| chr12:22651837
|
C | G | 1 | a0001c0001t0003g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.417-7177C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651837 | ||||||
| chr12:22651850
|
C | T | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.417-7164C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651850 | ||||||
| chr12:22651966
|
G | A | 4 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0016g0016others(1): Show | 7 | HG02129.hp2 HG03704.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.417-7048G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651966 | ||||||
| chr12:22651970
|
G | A | 86 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(83): Show | 102 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.417-7044G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651970 | ||||||
| chr12:22651992
|
A | G | 2 | a0001c0002t0001g0016a0001c0002t0016g0016 | 2 | HG02129.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.417-7022A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22651992 | ||||||
| chr12:22652095
|
G | A | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-6919G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652095 | ||||||
| chr12:22652193
|
A | T | 64 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(61): Show | 75 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.417-6821A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652193 | ||||||
| chr12:22652360
|
G | A | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.417-6654G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652360 | ||||||
| chr12:22652387
|
A | G | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.417-6627A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652387 | ||||||
| chr12:22652540
|
T | C | 1 | a0001c0002t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.417-6474T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652540 | ||||||
| chr12:22652622
|
T | A | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.417-6392T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652622 | ||||||
| chr12:22652624
|
A | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-6390A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652624 | ||||||
| chr12:22652705
|
A | T | 1 | a0001c0002t0002g0121 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.417-6309A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652705 | ||||||
| chr12:22652708
|
TGTG | T | 10 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(7): Show | 11 | HG00408.hp2 HG00673.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.417-6304_417-6302d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22652708 | |||||
| chr12:22652825
|
T | C | 1 | a0001c0003t0007g0112 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.417-6189T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652825 | ||||||
| chr12:22652843
|
C | T | 1 | a0001c0002t0005g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.417-6171C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652843 | ||||||
| chr12:22652947
|
A | C | 16 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(13): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.417-6067A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22652947 | ||||||
| chr12:22653047
|
T | C | 1 | a0001c0001t0005g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.417-5967T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653047 | ||||||
| chr12:22653099
|
T | C | 1 | a0001c0001t0005g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.417-5915T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653099 | ||||||
| chr12:22653214
|
G | A | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-5800G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653214 | ||||||
| chr12:22653606
|
C | T | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.417-5408C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653606 | ||||||
| chr12:22653721
|
T | C | 36 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(33): Show | 45 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.417-5293T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653721 | ||||||
| chr12:22653742
|
A | G | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.417-5272A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653742 | ||||||
| chr12:22653894
|
A | T | 1 | a0001c0001t0003g0156 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.417-5120A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653894 | ||||||
| chr12:22653991
|
A | T | 1 | a0001c0001t0007g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.417-5023A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22653991 | ||||||
| chr12:22654053
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.417-4961A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654053 | ||||||
| chr12:22654122
|
A | G | 17 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(14): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-4892A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654122 | ||||||
| chr12:22654141
|
T | A | 17 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(14): Show | 21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.417-4873T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654141 | ||||||
| chr12:22654326
|
C | G | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-4688C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654326 | ||||||
| chr12:22654399
|
G | C | 1 | a0001c0001t0002g0053 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.417-4615G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654399 | ||||||
| chr12:22654460
|
A | C | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-4554A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654460 | ||||||
| chr12:22654556
|
A | T | 17 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(14): Show | 18 | HG00544.hp1 HG00673.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.417-4458A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654556 | ||||||
| chr12:22654773
|
T | TAAC | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-4238_417-4236d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22654773 | |||||
| chr12:22654957
|
A | G | 1 | a0003c0006t0002g0119 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.417-4057A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22654957 | ||||||
| chr12:22655156
|
C | CG | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3854dupG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655156 | |||||
| chr12:22655209
|
T | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3805T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655209 | ||||||
| chr12:22655212
|
T | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3802T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655212 | ||||||
| chr12:22655328
|
GT | G | 14 | a0001c0001t0002g0053a0001c0001t0007g0256a0001c0001t0008g0054others(11): Show | 15 | HG00673.hp2 HG01884.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.417-3662delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655328 | |||||
| chr12:22655328
|
GTT | G | 45 | a0001c0001t0002g0036a0001c0001t0004g0111a0001c0001t0004g0249others(42): Show | 51 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.417-3663_417-3662d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655328 | |||||
| chr12:22655328
|
GTTT | G | 202 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(199): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.417-3664_417-3662d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22655328 | |||||
| chr12:22655332
|
T | G | 1 | a0001c0001t0008g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.417-3682T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655332 | ||||||
| chr12:22655333
|
T | G | 10 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(7): Show | 11 | HG00673.hp2 HG03516.hp1 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.417-3681T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655333 | ||||||
| chr12:22655334
|
T | G | 26 | a0001c0001t0008g0025a0001c0001t0008g0187a0001c0001t0008g0188others(23): Show | 32 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.417-3680T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655334 | ||||||
| chr12:22655337
|
T | G | 1 | a0001c0002t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.417-3677T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655337 | ||||||
| chr12:22655338
|
T | G | 132 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(129): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.417-3676T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655338 | ||||||
| chr12:22655339
|
T | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3675T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655339 | ||||||
| chr12:22655346
|
T | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-3668T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655346 | ||||||
| chr12:22655358
|
C | T | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.417-3656C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655358 | ||||||
| chr12:22655367
|
G | A | 2 | a0001c0001t0040g0049a0001c0001t0047g0052 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.417-3647G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655367 | ||||||
| chr12:22655483
|
C | T | 3 | a0001c0003t0007g0112a0001c0003t0011g0017a0001c0003t0011g0113 | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.417-3531C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655483 | ||||||
| chr12:22655638
|
A | T | 1 | a0001c0002t0001g0084 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.417-3376A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655638 | ||||||
| chr12:22655710
|
C | A | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-3304C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655710 | ||||||
| chr12:22655829
|
C | T | 1 | a0001c0002t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.417-3185C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655829 | ||||||
| chr12:22655921
|
G | A | 2 | a0001c0002t0001g0109a0001c0002t0001g0118 | 2 | HG00639.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.417-3093G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22655921 | ||||||
| chr12:22656097
|
G | T | 3 | a0001c0001t0017g0239a0001c0001t0017g0240a0001c0001t0017g0241 | 3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.417-2917G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656097 | ||||||
| chr12:22656209
|
A | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-2805A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656209 | ||||||
| chr12:22656242
|
T | C | 1 | a0001c0001t0007g0125 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.417-2772T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656242 | ||||||
| chr12:22656440
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.417-2574A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656440 | ||||||
| chr12:22656603
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.417-2411C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656603 | ||||||
| chr12:22656639
|
C | T | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.417-2375C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656639 | ||||||
| chr12:22656784
|
A | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-2230A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22656784 | ||||||
| chr12:22657062
|
T | G | 1 | a0001c0001t0002g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.417-1952T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657062 | ||||||
| chr12:22657088
|
G | T | 3 | a0001c0001t0017g0239a0001c0001t0017g0240a0001c0001t0017g0241 | 3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.417-1926G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657088 | ||||||
| chr12:22657135
|
C | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-1879C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657135 | ||||||
| chr12:22657145
|
A | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-1869A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657145 | ||||||
| chr12:22657445
|
G | C | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.417-1569G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657445 | ||||||
| chr12:22657539
|
A | G | 1 | a0001c0002t0002g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.417-1475A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657539 | ||||||
| chr12:22657607
|
A | AT | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.417-1403dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22657607 | |||||
| chr12:22657739
|
C | T | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.417-1275C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657739 | ||||||
| chr12:22657895
|
C | T | 1 | a0001c0001t0013g0200 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.417-1119C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657895 | ||||||
| chr12:22657949
|
C | T | 1 | a0001c0002t0001g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.417-1065C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22657949 | ||||||
| chr12:22658126
|
A | G | 1 | a0001c0001t0003g0022 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.417-888A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658126 | ||||||
| chr12:22658128
|
CAAG | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-883_417-881del others(3): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 22658128 | |||||
| chr12:22658218
|
A | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-796A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658218 | ||||||
| chr12:22658266
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.417-748C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658266 | ||||||
| chr12:22658366
|
T | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-648T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658366 | ||||||
| chr12:22658439
|
A | T | 1 | a0001c0001t0002g0226 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.417-575A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658439 | ||||||
| chr12:22658512
|
C | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.417-502C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658512 | ||||||
| chr12:22658607
|
A | G | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.417-407A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658607 | ||||||
| chr12:22658685
|
C | T | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.417-329C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658685 | ||||||
| chr12:22658833
|
A | G | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.417-181A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658833 | ||||||
| chr12:22658898
|
G | A | 1 | a0001c0002t0005g0087 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.417-116G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658898 | ||||||
| chr12:22658918
|
G | A | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.417-96G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 2/7 | chr12 | 22658918 | ||||||
| chr12:22659316
|
A | G | 1 | a0001c0002t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.557+162A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659316 | ||||||
| chr12:22659335
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.557+181C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659335 | ||||||
| chr12:22659337
|
C | T | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557+183C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659337 | ||||||
| chr12:22659421
|
T | G | 260 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(257): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.557+267T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659421 | ||||||
| chr12:22659506
|
A | C | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.557+352A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659506 | ||||||
| chr12:22659699
|
A | C | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557+545A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659699 | ||||||
| chr12:22659832
|
A | G | 147 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(144): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.557+678A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659832 | ||||||
| chr12:22659984
|
T | TA | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.557+830_557+831ins others(1): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659984 | ||||||
| chr12:22659998
|
C | A | 2 | a0001c0001t0002g0093a0001c0001t0007g0098 | 2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.557+844C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22659998 | ||||||
| chr12:22660022
|
C | A | 1 | a0001c0002t0001g0221 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.557+868C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660022 | ||||||
| chr12:22660034
|
T | TA | 6 | a0001c0001t0002g0226a0001c0001t0028g0046a0001c0001t0028g0047others(3): Show | 6 | HG01257.hp2 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.557+901dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 22660034 | |||||
| chr12:22660034
|
TA | T | 30 | a0001c0001t0001g0210a0001c0001t0002g0204a0001c0001t0002g0225others(27): Show | 34 | HG00099.hp1 HG00323.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.557+901delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 22660034 | |||||
| chr12:22660034
|
TAA | T | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.557+900_557+901del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 22660034 | |||||
| chr12:22660047
|
A | C | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.557+893A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660047 | ||||||
| chr12:22660048
|
A | C | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.557+894A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660048 | ||||||
| chr12:22660060
|
G | A | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.557+906G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660060 | ||||||
| chr12:22660117
|
G | A | 1 | a0001c0001t0004g0252 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.558-946G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660117 | ||||||
| chr12:22660309
|
C | T | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.558-754C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660309 | ||||||
| chr12:22660354
|
G | A | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.558-709G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660354 | ||||||
| chr12:22660359
|
A | G | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.558-704A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660359 | ||||||
| chr12:22660397
|
T | C | 1 | a0001c0001t0056g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.558-666T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660397 | ||||||
| chr12:22660401
|
G | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.558-662G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660401 | ||||||
| chr12:22660489
|
C | T | 1 | a0001c0002t0001g0178 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.558-574C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660489 | ||||||
| chr12:22660653
|
T | A | 5 | a0001c0002t0005g0009a0002c0004t0001g0009a0002c0004t0001g0062others(2): Show | 5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.558-410T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660653 | ||||||
| chr12:22660668
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.558-395G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660668 | ||||||
| chr12:22660965
|
G | T | 1 | a0001c0009t0023g0152 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.558-98G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22660965 | ||||||
| chr12:22661036
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.558-27A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 3/7 | chr12 | 22661036 | ||||||
| chr12:22661296
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.700+91T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661296 | ||||||
| chr12:22661392
|
A | G | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.700+187A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661392 | ||||||
| chr12:22661519
|
A | G | 1 | a0001c0001t0024g0248 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.700+314A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661519 | ||||||
| chr12:22661904
|
T | C | 1 | a0001c0002t0001g0131 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.700+699T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22661904 | ||||||
| chr12:22662053
|
CGCA | C | 8 | a0001c0001t0009g0001a0001c0001t0009g0139a0001c0001t0009g0144others(5): Show | 12 | HG01891.hp2 HG02257.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.700+849_700+851del others(3): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662053 | ||||||
| chr12:22662056
|
A | C | 1 | a0001c0001t0014g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.700+851A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662056 | ||||||
| chr12:22662056
|
AC | A | 16 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0188others(13): Show | 17 | HG00544.hp1 HG00673.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.700+862delC | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662056 | |||||
| chr12:22662056
|
ACC | A | 225 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(222): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.700+861_700+862del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662056 | |||||
| chr12:22662061
|
C | G | 1 | a0001c0001t0005g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.700+856C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662061 | ||||||
| chr12:22662067
|
C | T | 1 | a0001c0002t0016g0058 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.700+862C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662067 | ||||||
| chr12:22662077
|
C | T | 78 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(75): Show | 94 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.700+872C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662077 | ||||||
| chr12:22662088
|
A | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+883A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662088 | ||||||
| chr12:22662234
|
A | C | 4 | a0001c0001t0009g0138a0001c0001t0009g0139a0001c0001t0014g0140others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+1029A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662234 | ||||||
| chr12:22662242
|
A | AT | 37 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(34): Show | 39 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.700+1062dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662242 | |||||
| chr12:22662242
|
AT | A | 12 | a0001c0001t0002g0036a0001c0001t0002g0094a0001c0001t0002g0212others(9): Show | 12 | HG00099.hp1 HG00280.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.700+1062delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662242 | |||||
| chr12:22662276
|
T | G | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.700+1071T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662276 | ||||||
| chr12:22662353
|
G | A | 4 | a0001c0001t0017g0239a0001c0001t0017g0240a0001c0001t0017g0241others(1): Show | 4 | HG01891.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.700+1148G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662353 | ||||||
| chr12:22662389
|
TTCC | T | 11 | a0001c0001t0009g0001a0001c0001t0009g0144a0001c0001t0009g0146others(8): Show | 15 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.700+1186_700+1188d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662389 | |||||
| chr12:22662390
|
TCC | T | 4 | a0001c0001t0009g0138a0001c0001t0009g0139a0001c0001t0014g0140others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+1186_700+1187d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662390 | ||||||
| chr12:22662392
|
C | CT | 139 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(136): Show | 163 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.700+1204dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22662392 | |||||
| chr12:22662394
|
T | C | 4 | a0001c0001t0009g0138a0001c0001t0009g0139a0001c0001t0014g0140others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.700+1189T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662394 | ||||||
| chr12:22662395
|
T | C | 11 | a0001c0001t0009g0001a0001c0001t0009g0144a0001c0001t0009g0146others(8): Show | 15 | HG01891.hp2 HG02257.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.700+1190T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662395 | ||||||
| chr12:22662678
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.700+1473G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662678 | ||||||
| chr12:22662769
|
A | T | 1 | a0001c0001t0014g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.700+1564A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662769 | ||||||
| chr12:22662853
|
G | A | 3 | a0001c0001t0017g0239a0001c0001t0017g0240a0001c0001t0017g0241 | 3 | HG01891.hp1 HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.700+1648G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662853 | ||||||
| chr12:22662993
|
T | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+1788T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22662993 | ||||||
| chr12:22663068
|
G | A | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.700+1863G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663068 | ||||||
| chr12:22663411
|
C | T | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.700+2206C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663411 | ||||||
| chr12:22663470
|
A | C | 3 | a0001c0001t0002g0218a0001c0001t0043g0233a0001c0001t0050g0217 | 3 | HG00741.hp1 HG01071.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.700+2265A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663470 | ||||||
| chr12:22663553
|
G | GT | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+2349dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22663553 | |||||
| chr12:22663769
|
T | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.700+2564T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663769 | ||||||
| chr12:22663860
|
T | C | 7 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0012g0003others(4): Show | 10 | HG01243.hp2 HG02258.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.700+2655T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663860 | ||||||
| chr12:22663922
|
C | T | 1 | a0001c0001t0010g0170 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.700+2717C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663922 | ||||||
| chr12:22663943
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700+2738T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22663943 | ||||||
| chr12:22664037
|
G | A | 1 | a0001c0001t0004g0250 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.700+2832G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664037 | ||||||
| chr12:22664169
|
T | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.700+2964T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664169 | ||||||
| chr12:22664330
|
A | G | 1 | a0001c0002t0001g0080 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.700+3125A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664330 | ||||||
| chr12:22664345
|
A | G | 1 | a0001c0001t0007g0208 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.700+3140A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664345 | ||||||
| chr12:22664604
|
T | A | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.700+3399T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664604 | ||||||
| chr12:22664691
|
T | C | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.700+3486T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664691 | ||||||
| chr12:22664925
|
A | T | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.700+3720A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22664925 | ||||||
| chr12:22665130
|
C | T | 1 | a0001c0001t0005g0108 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.700+3925C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665130 | ||||||
| chr12:22665174
|
T | C | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.700+3969T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665174 | ||||||
| chr12:22665280
|
G | A | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.700+4075G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665280 | ||||||
| chr12:22665322
|
C | T | 1 | a0001c0001t0007g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.700+4117C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665322 | ||||||
| chr12:22665396
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.700+4191A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22665396 | ||||||
| chr12:22666033
|
T | C | 1 | a0001c0001t0007g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.700+4828T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666033 | ||||||
| chr12:22666079
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.700+4874C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666079 | ||||||
| chr12:22666097
|
C | G | 3 | a0001c0001t0008g0188a0001c0001t0008g0189a0001c0001t0008g0193 | 3 | NA18998.hp2 NA19057.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.700+4892C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666097 | ||||||
| chr12:22666169
|
A | G | 1 | a0001c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.700+4964A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666169 | ||||||
| chr12:22666301
|
G | A | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.701-4971G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666301 | ||||||
| chr12:22666416
|
TA | T | 8 | a0001c0002t0002g0019a0001c0002t0002g0020a0001c0002t0002g0121others(5): Show | 11 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.701-4853delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22666416 | |||||
| chr12:22666432
|
C | T | 164 | a0001c0001t0001g0083a0001c0001t0001g0210a0001c0001t0002g0004others(161): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.701-4840C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666432 | ||||||
| chr12:22666520
|
A | G | 28 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(25): Show | 34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.701-4752A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666520 | ||||||
| chr12:22666589
|
G | C | 69 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(66): Show | 81 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.701-4683G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666589 | ||||||
| chr12:22666860
|
T | C | 1 | a0003c0006t0001g0086 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.701-4412T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666860 | ||||||
| chr12:22666959
|
A | T | 84 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(81): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.701-4313A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22666959 | ||||||
| chr12:22667172
|
G | A | 1 | a0001c0002t0002g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.701-4100G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667172 | ||||||
| chr12:22667250
|
A | G | 2 | a0001c0002t0005g0087a0001c0002t0005g0088 | 2 | NA18949.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.701-4022A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667250 | ||||||
| chr12:22667310
|
C | T | 84 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(81): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.701-3962C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667310 | ||||||
| chr12:22667416
|
G | A | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-3856G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667416 | ||||||
| chr12:22667463
|
G | A | 1 | a0003c0006t0058g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.701-3809G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22667463 | ||||||
| chr12:22668116
|
C | T | 1 | a0001c0002t0021g0070 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.701-3156C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22668116 | ||||||
| chr12:22668150
|
T | A | 2 | a0001c0001t0002g0093a0001c0001t0007g0098 | 2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.701-3122T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22668150 | ||||||
| chr12:22668492
|
GT | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0226a0001c0001t0044g0027 | 3 | HG00639.hp1 HG01071.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.701-2777delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22668492 | |||||
| chr12:22669053
|
T | C | 3 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0172 | 3 | NA18945.hp2 NA18954.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.701-2219T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22669053 | ||||||
| chr12:22669201
|
ATC | A | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-2067_701-2066d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669201 | |||||
| chr12:22669339
|
G | GA | 84 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(81): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.701-1927dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669339 | |||||
| chr12:22669436
|
T | TC | 5 | a0001c0001t0013g0197a0001c0001t0013g0198a0001c0001t0013g0199others(2): Show | 5 | HG02922.hp1 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.701-1835dupC | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669436 | |||||
| chr12:22669472
|
C | G | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-1800C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22669472 | ||||||
| chr12:22669686
|
T | C | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.701-1586T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22669686 | ||||||
| chr12:22669821
|
GA | G | 84 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(81): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.701-1443delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22669821 | |||||
| chr12:22670147
|
T | C | 1 | a0001c0002t0026g0205 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.701-1125T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670147 | ||||||
| chr12:22670369
|
A | AT | 19 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(16): Show | 25 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.701-889dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22670369 | |||||
| chr12:22670369
|
AT | A | 22 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(19): Show | 27 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.701-889delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22670369 | |||||
| chr12:22670369
|
ATT | A | 48 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(45): Show | 55 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.701-890_701-889del others(2): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 22670369 | |||||
| chr12:22670417
|
C | T | 1 | a0001c0002t0002g0122 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.701-855C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670417 | ||||||
| chr12:22670508
|
C | T | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.701-764C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670508 | ||||||
| chr12:22670519
|
T | C | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.701-753T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670519 | ||||||
| chr12:22670530
|
T | C | 28 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(25): Show | 34 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.701-742T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670530 | ||||||
| chr12:22670733
|
G | A | 69 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(66): Show | 81 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.701-539G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22670733 | ||||||
| chr12:22671074
|
C | A | 1 | a0001c0005t0052g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.701-198C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 4/7 | chr12 | 22671074 | ||||||
| chr12:22671444
|
G | C | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.784+89G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671444 | ||||||
| chr12:22671568
|
G | A | 5 | a0001c0002t0005g0009a0002c0004t0001g0009a0002c0004t0001g0062others(2): Show | 5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+213G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671568 | ||||||
| chr12:22671620
|
C | T | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.784+265C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671620 | ||||||
| chr12:22671680
|
T | C | 1 | a0001c0002t0001g0068 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.784+325T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671680 | ||||||
| chr12:22671705
|
G | C | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.784+350G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671705 | ||||||
| chr12:22671815
|
G | A | 52 | a0001c0001t0001g0210a0001c0001t0002g0004a0001c0001t0002g0026others(49): Show | 57 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.784+460G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671815 | ||||||
| chr12:22671817
|
C | T | 16 | a0001c0001t0004g0245a0001c0001t0009g0001a0001c0001t0009g0138others(13): Show | 20 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.784+462C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671817 | ||||||
| chr12:22671820
|
T | C | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+465T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671820 | ||||||
| chr12:22671841
|
T | TA | 10 | a0001c0001t0002g0223a0001c0001t0007g0095a0001c0001t0007g0202others(7): Show | 10 | HG01433.hp1 HG02027.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+508dupA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 22671841 | |||||
| chr12:22671841
|
T | TAAAAA | 12 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(9): Show | 16 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.784+504_784+508dup others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 22671841 | |||||
| chr12:22671841
|
TA | T | 12 | a0001c0001t0001g0182a0001c0001t0001g0210a0001c0001t0002g0211others(9): Show | 12 | HG00323.hp2 HG03491.hp2 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.784+508delA | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 22671841 | |||||
| chr12:22671866
|
A | C | 1 | a0001c0001t0009g0139 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784+511A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671866 | ||||||
| chr12:22671968
|
C | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+613C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671968 | ||||||
| chr12:22671977
|
A | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.784+622A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22671977 | ||||||
| chr12:22672288
|
C | A | 1 | a0001c0001t0002g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.784+933C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672288 | ||||||
| chr12:22672575
|
C | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.785-925C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672575 | ||||||
| chr12:22672703
|
G | A | 1 | a0001c0001t0023g0037 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.785-797G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672703 | ||||||
| chr12:22672760
|
C | T | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.785-740C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22672760 | ||||||
| chr12:22673001
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.785-499T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22673001 | ||||||
| chr12:22673345
|
T | C | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.785-155T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 5/7 | chr12 | 22673345 | ||||||
| chr12:22673797
|
T | A | 1 | a0001c0001t0011g0103 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.945+137T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22673797 | ||||||
| chr12:22673817
|
T | A | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(40): Show | 50 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.945+157T>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22673817 | ||||||
| chr12:22673839
|
A | C | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.945+179A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22673839 | ||||||
| chr12:22674408
|
G | A | 2 | a0001c0002t0001g0068a0001c0002t0016g0048 | 2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.945+748G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674408 | ||||||
| chr12:22674561
|
A | C | 2 | a0001c0001t0002g0218a0001c0001t0043g0233 | 2 | HG01071.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.945+901A>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674561 | ||||||
| chr12:22674678
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.945+1018A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674678 | ||||||
| chr12:22674959
|
C | T | 84 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(81): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.945+1299C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22674959 | ||||||
| chr12:22675002
|
C | T | 1 | a0001c0001t0008g0192 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.945+1342C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675002 | ||||||
| chr12:22675221
|
A | G | 6 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043others(3): Show | 6 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.945+1561A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675221 | ||||||
| chr12:22675222
|
AT | A | 69 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(66): Show | 81 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.945+1569delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22675222 | |||||
| chr12:22675377
|
A | T | 1 | a0001c0001t0002g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.945+1717A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675377 | ||||||
| chr12:22675418
|
C | T | 1 | a0001c0001t0007g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.945+1758C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675418 | ||||||
| chr12:22675620
|
G | A | 1 | a0001c0002t0005g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.945+1960G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675620 | ||||||
| chr12:22675758
|
A | G | 3 | a0001c0001t0018g0039a0001c0001t0018g0040a0001c0001t0018g0043 | 3 | HG01168.hp1 HG01169.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.945+2098A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675758 | ||||||
| chr12:22675875
|
T | C | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.945+2215T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22675875 | ||||||
| chr12:22676051
|
G | A | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.945+2391G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676051 | ||||||
| chr12:22676094
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.945+2434T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676094 | ||||||
| chr12:22676404
|
A | G | 2 | a0001c0001t0025g0033a0001c0001t0025g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.945+2744A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676404 | ||||||
| chr12:22676471
|
G | A | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945+2811G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676471 | ||||||
| chr12:22676725
|
T | C | 1 | a0001c0001t0032g0257 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.945+3065T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22676725 | ||||||
| chr12:22676856
|
GT | G | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.945+3206delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22676856 | |||||
| chr12:22676856
|
GTT | G | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.945+3205_945+3206d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22676856 | |||||
| chr12:22677066
|
A | G | 4 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0001t0010g0159others(1): Show | 4 | NA18965.hp2 NA18967.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+3406A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677066 | ||||||
| chr12:22677091
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.945+3431G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677091 | ||||||
| chr12:22677574
|
G | A | 3 | a0001c0001t0003g0154a0001c0001t0003g0155a0001c0001t0003g0168 | 3 | HG01257.hp1 HG01258.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.945+3914G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677574 | ||||||
| chr12:22677764
|
C | T | 41 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(38): Show | 48 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.945+4104C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677764 | ||||||
| chr12:22677828
|
G | A | 69 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(66): Show | 81 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.945+4168G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677828 | ||||||
| chr12:22677964
|
C | T | 1 | a0001c0002t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.945+4304C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22677964 | ||||||
| chr12:22678251
|
C | T | 134 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(131): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.945+4591C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678251 | ||||||
| chr12:22678356
|
A | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.945+4696A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678356 | ||||||
| chr12:22678425
|
A | G | 1 | a0001c0002t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.945+4765A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678425 | ||||||
| chr12:22678529
|
G | A | 84 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(81): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.945+4869G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678529 | ||||||
| chr12:22678617
|
A | G | 2 | a0001c0001t0003g0155a0001c0001t0003g0168 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.945+4957A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678617 | ||||||
| chr12:22678781
|
A | G | 15 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(12): Show | 19 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.945+5121A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678781 | ||||||
| chr12:22678858
|
G | T | 1 | a0001c0002t0039g0130 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.945+5198G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678858 | ||||||
| chr12:22678925
|
A | G | 1 | a0001c0001t0035g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.945+5265A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22678925 | ||||||
| chr12:22679301
|
T | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-5182T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679301 | ||||||
| chr12:22679320
|
G | T | 1 | a0001c0001t0003g0175 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.946-5163G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679320 | ||||||
| chr12:22679444
|
C | CT | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-5039_946-5038i others(3): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679444 | ||||||
| chr12:22679616
|
G | T | 1 | a0001c0001t0018g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.946-4867G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679616 | ||||||
| chr12:22679627
|
G | T | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-4856G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679627 | ||||||
| chr12:22679670
|
C | T | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.946-4813C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679670 | ||||||
| chr12:22679701
|
TG | T | 13 | a0001c0001t0009g0001a0001c0001t0009g0139a0001c0001t0009g0144others(10): Show | 17 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.946-4781delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679701 | ||||||
| chr12:22679702
|
G | GT | 23 | a0001c0001t0001g0183a0001c0001t0002g0092a0001c0001t0002g0093others(20): Show | 24 | HG00673.hp2 HG01169.hp1 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.946-4765dupT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22679702 | |||||
| chr12:22679702
|
G | T | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-4781G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679702 | ||||||
| chr12:22679702
|
GT | G | 23 | a0001c0001t0003g0024a0001c0001t0003g0151a0001c0001t0004g0007others(20): Show | 29 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.946-4765delT | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22679702 | |||||
| chr12:22679702
|
GTT | G | 45 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(42): Show | 51 | HG00733.hp2 HG00741.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.946-4766_946-4765d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22679702 | |||||
| chr12:22679733
|
C | T | 1 | a0001c0001t0014g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.946-4750C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679733 | ||||||
| chr12:22679739
|
C | T | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-4744C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679739 | ||||||
| chr12:22679884
|
G | T | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-4599G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679884 | ||||||
| chr12:22679953
|
G | A | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-4530G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22679953 | ||||||
| chr12:22680012
|
AATAC | A | 84 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(81): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.946-4464_946-4461d others(6): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680012 | |||||
| chr12:22680120
|
G | A | 1 | a0001c0002t0005g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.946-4363G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680120 | ||||||
| chr12:22680202
|
G | A | 1 | a0001c0001t0055g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.946-4281G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680202 | ||||||
| chr12:22680291
|
T | G | 5 | a0001c0002t0005g0009a0002c0004t0001g0009a0002c0004t0001g0062others(2): Show | 5 | HG00408.hp1 NA18954.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.946-4192T>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680291 | ||||||
| chr12:22680430
|
C | G | 18 | a0001c0001t0008g0025a0001c0001t0008g0054a0001c0001t0008g0187others(15): Show | 19 | HG00544.hp1 HG00673.hp2 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.946-4053C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680430 | ||||||
| chr12:22680473
|
C | G | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-4010C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680473 | ||||||
| chr12:22680584
|
T | C | 1 | a0001c0001t0011g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.946-3899T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680584 | ||||||
| chr12:22680595
|
A | T | 1 | a0001c0001t0020g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.946-3888A>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680595 | ||||||
| chr12:22680723
|
T | C | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-3760T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680723 | ||||||
| chr12:22680754
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.946-3729C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680754 | ||||||
| chr12:22680889
|
TTC | T | 9 | a0001c0001t0004g0105a0001c0001t0004g0110a0001c0001t0004g0111others(6): Show | 10 | HG00558.hp2 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.946-3593_946-3592d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680889 | ||||||
| chr12:22680889
|
TTCC | T | 11 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0238others(8): Show | 15 | HG00323.hp1 HG00423.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.946-3593_946-3591d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680889 | ||||||
| chr12:22680890
|
T | TC | 65 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0002g0026others(62): Show | 67 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.946-3588dupC | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680890 | |||||
| chr12:22680890
|
T | TCC | 15 | a0001c0001t0001g0185a0001c0001t0002g0228a0001c0001t0007g0208others(12): Show | 15 | HG00408.hp1 HG00621.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.946-3589_946-3588d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680890 | |||||
| chr12:22680893
|
CCCG | C | 27 | a0001c0001t0003g0008a0001c0001t0003g0150a0001c0001t0003g0161others(24): Show | 34 | HG00733.hp2 HG01175.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.946-3587_946-3585d others(5): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680893 | |||||
| chr12:22680894
|
CCG | C | 20 | a0001c0001t0002g0092a0001c0001t0003g0013a0001c0001t0003g0022others(17): Show | 23 | HG01074.hp2 HG01081.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.946-3587_946-3586d others(4): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22680894 | |||||
| chr12:22680895
|
C | A | 1 | a0001c0001t0007g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.946-3588C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680895 | ||||||
| chr12:22680895
|
CG | C | 32 | a0001c0001t0001g0014a0001c0001t0001g0179a0001c0001t0001g0183others(29): Show | 35 | HG00741.hp2 HG01081.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.946-3587delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680895 | ||||||
| chr12:22680896
|
G | C | 189 | a0001c0001t0001g0083a0001c0001t0001g0182a0001c0001t0001g0184others(186): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.946-3587G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680896 | ||||||
| chr12:22680896
|
G | T | 3 | a0001c0003t0007g0112a0001c0003t0011g0017a0001c0003t0011g0113 | 4 | HG01884.hp2 HG02451.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.946-3587G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680896 | ||||||
| chr12:22680897
|
C | A | 1 | a0001c0001t0019g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946-3586C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680897 | ||||||
| chr12:22680900
|
C | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-3583C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680900 | ||||||
| chr12:22680905
|
T | C | 49 | a0001c0001t0002g0036a0001c0001t0003g0008a0001c0001t0003g0013others(46): Show | 56 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.946-3578T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22680905 | ||||||
| chr12:22681205
|
TG | T | 47 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(44): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.946-3276delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22681205 | |||||
| chr12:22681472
|
G | A | 1 | a0001c0001t0014g0141 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.946-3011G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22681472 | ||||||
| chr12:22681843
|
T | C | 2 | a0001c0001t0028g0046a0001c0001t0028g0047 | 2 | HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.946-2640T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22681843 | ||||||
| chr12:22682145
|
C | A | 1 | a0001c0002t0001g0080 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.946-2338C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22682145 | ||||||
| chr12:22682399
|
T | C | 1 | a0001c0001t0002g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.946-2084T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22682399 | ||||||
| chr12:22682730
|
CCTTGA | C | 19 | a0001c0001t0001g0210a0001c0002t0001g0059a0001c0002t0001g0069others(16): Show | 19 | HG00408.hp1 HG00639.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.946-1749_946-1745d others(7): Show |
ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 22682730 | |||||
| chr12:22683118
|
G | T | 70 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(67): Show | 82 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.946-1365G>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683118 | ||||||
| chr12:22683553
|
C | G | 16 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(13): Show | 20 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.946-930C>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683553 | ||||||
| chr12:22683845
|
G | C | 1 | a0001c0001t0003g0148 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.946-638G>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683845 | ||||||
| chr12:22683965
|
A | G | 44 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0022others(41): Show | 51 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.946-518A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22683965 | ||||||
| chr12:22684007
|
G | A | 173 | a0001c0001t0001g0014a0001c0001t0001g0083a0001c0001t0001g0179others(170): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.946-476G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684007 | ||||||
| chr12:22684027
|
A | G | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-456A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684027 | ||||||
| chr12:22684166
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.946-317T>C | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684166 | ||||||
| chr12:22684219
|
A | G | 4 | a0001c0002t0001g0011a0001c0002t0001g0080a0001c0002t0001g0089others(1): Show | 6 | HG00558.hp1 HG02132.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.946-264A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684219 | ||||||
| chr12:22684308
|
G | A | 1 | a0001c0001t0034g0135 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-175G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684308 | ||||||
| chr12:22684323
|
C | T | 14 | a0001c0001t0009g0001a0001c0001t0009g0138a0001c0001t0009g0139others(11): Show | 18 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.946-160C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684323 | ||||||
| chr12:22684327
|
CG | C | 3 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0172 | 3 | NA18945.hp2 NA18954.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.946-155delG | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684327 | ||||||
| chr12:22684348
|
A | G | 21 | a0001c0001t0004g0007a0001c0001t0004g0032a0001c0001t0004g0105others(18): Show | 26 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.946-135A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684348 | ||||||
| chr12:22684388
|
A | G | 2 | a0001c0001t0014g0136a0001c0001t0014g0137 | 2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.946-95A>G | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684388 | ||||||
| chr12:22684475
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.946-8C>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 6/7 | chr12 | 22684475 | ||||||
| chr12:22684583
|
C | T | 1 | a0001c0001t0020g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1019+27C>T | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 7/7 | chr12 | 22684583 | ||||||
| chr12:22684718
|
G | A | 1 | a0001c0001t0003g0157 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1019+162G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 7/7 | chr12 | 22684718 | ||||||
| chr12:22684791
|
G | A | 2 | a0001c0001t0029g0195a0001c0001t0029g0196 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1020-91G>A | ETNK1 | ENSG00000139163.16 | transcript | ENST00000266517.9 | protein_coding | 7/7 | chr12 | 22684791 |