Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 92797 |
|---|---|
| ensemblid | ENSG00000127311.10 |
| hgncid | 17196 |
| symbol | HELB |
| name | DNA helicase B |
| refseq_nuc | NM_001370285.1 |
| refseq_prot | NP_001357214.1 |
| ensembl_nuc | ENST00000247815.9 |
| ensembl_prot | ENSP00000247815.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 66302493 |
| end | 66338199 |
| strand | + |
| ver | v1.2 |
| region | chr12:66302493-66338199 |
| region5000 | chr12:66297493-66343199 |
| regionname0 | HELB_chr12_66302493_66338199 |
| regionname5000 | HELB_chr12_66297493_66343199 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1087 | 101 | 19 | 17 | 50 | 2 | 13 | 38 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002 | 0/0 | 1087 | 95 | 7 | 23 | 56 | 3 | 6 | 44 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0003 | 0/1 | 1087 | 51 | 2 | 11 | 29 | 1 | 7 | 22 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004 | 1/0 | 1087 | 48 | 12 | 5 | 21 | 2 | 7 | 13 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005 | 0/0 | 1087 | 20 | 9 | 3 | 6 | 0 | 2 | 6 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0006 | 0/0 | 1087 | 16 | 16 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0007 | 0/0 | 1087 | 8 | 7 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0008 | 0/0 | 1087 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0009 | 0/0 | 1087 | 5 | 1 | 2 | 2 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0010 | 0/0 | 1087 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0011 | 0/0 | 1087 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0012 | 0/0 | 1087 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0013 | 0/0 | 1087 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0014 | 0/0 | 1087 | 4 | 0 | 1 | 0 | 0 | 3 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0015 | 0/0 | 1087 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0016 | 0/0 | 1087 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0017 | 0/0 | 739 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0018 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0019 | 0/0 | 830 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0020 | 0/0 | 1087 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0021 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0022 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0023 | 0/0 | 1087 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0024 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0025 | 0/0 | 1087 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0026 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0027 | 0/0 | 1087 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3264 | 90 | 7 | 22 | 52 | 3 | 6 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0002 | 0/0 | 3264 | 61 | 6 | 16 | 29 | 2 | 8 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0003 | 0/1 | 3264 | 51 | 2 | 11 | 29 | 1 | 7 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0004 | 1/0 | 3264 | 38 | 4 | 3 | 21 | 2 | 7 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0005 | 0/0 | 3264 | 19 | 0 | 0 | 16 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0006 | 0/0 | 3264 | 11 | 0 | 3 | 6 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0007 | 0/0 | 3264 | 10 | 10 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0008 | 0/0 | 3264 | 8 | 6 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0009 | 0/0 | 3264 | 7 | 7 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0010 | 0/0 | 3264 | 6 | 6 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0011 | 0/0 | 3264 | 6 | 5 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0012 | 0/0 | 3264 | 5 | 0 | 0 | 5 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0013 | 0/0 | 3264 | 5 | 5 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0014 | 0/0 | 3264 | 4 | 1 | 2 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0015 | 0/0 | 3264 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0016 | 0/0 | 3264 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0017 | 0/0 | 3264 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0018 | 0/0 | 3264 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0019 | 0/0 | 3264 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0020 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0021 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0022 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0023 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0024 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0025 | 0/0 | 3264 | 3 | 0 | 0 | 0 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0026 | 0/0 | 3264 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0027 | 0/0 | 3264 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0028 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0029 | 0/0 | 3264 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0030 | 0/0 | 3264 | 2 | 1 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0031 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0032 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0033 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0034 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0035 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0036 | 0/0 | 3264 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0037 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0038 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0039 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0040 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0041 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0042 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0043 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0044 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0045 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0046 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0047 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0048 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0049 | 0/0 | 3264 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| c0050 | 0/0 | 3264 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/1 | 11 | 1 | 4 | 2 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0002 | 0/0 | 10 | 1 | 4 | 4 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0004 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0005 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0007 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0010 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0013 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0045 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0046 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3264 | 61 | 6 | 16 | 29 | 2 | 8 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0005 | 0/0 | 3264 | 19 | 0 | 0 | 16 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0012 | 0/0 | 3264 | 5 | 0 | 0 | 5 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0018 | 0/0 | 3264 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0022 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0024 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0029 | 0/0 | 3264 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0030 | 0/0 | 3264 | 2 | 1 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0046 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0050 | 0/0 | 3264 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002c0001 | 0/0 | 3264 | 90 | 7 | 22 | 52 | 3 | 6 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002c0017 | 0/0 | 3264 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002c0037 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0003c0003 | 0/1 | 3264 | 51 | 2 | 11 | 29 | 1 | 7 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0004 | 1/0 | 3264 | 38 | 4 | 3 | 21 | 2 | 7 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0008 | 0/0 | 3264 | 8 | 6 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0034 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0035 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0006 | 0/0 | 3264 | 11 | 0 | 3 | 6 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0015 | 0/0 | 3264 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0023 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0033 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0044 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0006c0007 | 0/0 | 3264 | 10 | 10 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0006c0010 | 0/0 | 3264 | 6 | 6 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0007c0009 | 0/0 | 3264 | 7 | 7 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0007c0043 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0008c0011 | 0/0 | 3264 | 6 | 5 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0009c0014 | 0/0 | 3264 | 4 | 1 | 2 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0009c0047 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0010c0013 | 0/0 | 3264 | 5 | 5 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0011c0020 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0011c0027 | 0/0 | 3264 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0012c0016 | 0/0 | 3264 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0013c0019 | 0/0 | 3264 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0014c0025 | 0/0 | 3264 | 3 | 0 | 0 | 0 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0014c0048 | 0/0 | 3264 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0015c0026 | 0/0 | 3264 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0016c0021 | 0/0 | 3264 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0017c0028 | 0/0 | 3264 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0018c0039 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0019c0038 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0020c0036 | 0/0 | 3264 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0021c0040 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0022c0041 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0023c0032 | 0/0 | 3264 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0024c0045 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0025c0049 | 0/0 | 3264 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0026c0042 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0027c0031 | 0/0 | 3264 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 3472 | 61 | 6 | 16 | 29 | 2 | 8 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0005t0001 | 0/0 | 3472 | 19 | 0 | 0 | 16 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0012t0001 | 0/0 | 3472 | 5 | 0 | 0 | 5 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0018t0001 | 0/0 | 3472 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0022t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0024t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0029t0001 | 0/0 | 3472 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0030t0001 | 0/0 | 3472 | 2 | 1 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0046t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0001c0050t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002c0001t0001 | 0/0 | 3472 | 61 | 6 | 14 | 34 | 3 | 4 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002c0001t0002 | 0/0 | 3471 | 29 | 1 | 8 | 18 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002c0017t0001 | 0/0 | 3472 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0002c0037t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0003c0003t0001 | 0/1 | 3472 | 50 | 2 | 11 | 28 | 1 | 7 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0003c0003t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0004t0001 | 1/0 | 3472 | 38 | 4 | 3 | 21 | 2 | 7 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0008t0001 | 0/0 | 3472 | 8 | 6 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0034t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0004c0035t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0006t0001 | 0/0 | 3472 | 7 | 0 | 3 | 2 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0006t0002 | 0/0 | 3471 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0015t0001 | 0/0 | 3472 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0023t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0033t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0005c0044t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0006c0007t0001 | 0/0 | 3472 | 10 | 10 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0006c0010t0001 | 0/0 | 3472 | 6 | 6 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0007c0009t0001 | 0/0 | 3472 | 7 | 7 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0007c0043t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0008c0011t0001 | 0/0 | 3472 | 6 | 5 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0009c0014t0001 | 0/0 | 3472 | 4 | 1 | 2 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0009c0047t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0010c0013t0001 | 0/0 | 3472 | 5 | 5 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0011c0020t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0011c0027t0001 | 0/0 | 3472 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0012c0016t0001 | 0/0 | 3472 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0013c0019t0001 | 0/0 | 3472 | 4 | 4 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0014c0025t0001 | 0/0 | 3472 | 3 | 0 | 0 | 0 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0014c0048t0001 | 0/0 | 3472 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0015c0026t0001 | 0/0 | 3472 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0016c0021t0001 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0017c0028t0001 | 0/0 | 3472 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0018c0039t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0019c0038t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0020c0036t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0021c0040t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0022c0041t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0023c0032t0001 | 0/0 | 3472 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0024c0045t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0025c0049t0001 | 0/0 | 3472 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0026c0042t0002 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| a0027c0031t0001 | 0/0 | 3472 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | copy fasta | chr12 | 66297493 | 66343199 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0002 | 0/0 | 9 | 1 | 4 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0003 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0012t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0012t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0012t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0012t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0018t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0018t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0018t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0022t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0022t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0022t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0024t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0024t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0024t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0029t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0029t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0030t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0030t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0046t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0001c0050t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0007 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0017t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0017t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0017t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0002c0037t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0001 | 0/1 | 10 | 0 | 4 | 2 | 0 | 3 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0003c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0008t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0034t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0004c0035t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0006t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0015t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0015t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0015t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0015t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0023t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0023t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0023t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0033t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0005c0044t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0007t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0010t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0010t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0010t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0006c0010t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0007c0009t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0007c0009t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0007c0009t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0007c0009t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0007c0009t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0007c0009t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0007c0043t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0008c0011t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0008c0011t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0008c0011t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0008c0011t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0008c0011t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0009c0014t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0009c0014t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0009c0014t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0009c0014t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0009c0047t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0010c0013t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0010c0013t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0010c0013t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0010c0013t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0010c0013t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0011c0020t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0011c0020t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0011c0020t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0011c0027t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0011c0027t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0012c0016t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0012c0016t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0012c0016t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0012c0016t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0013c0019t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0013c0019t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0013c0019t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0014c0025t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0014c0025t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0014c0025t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0014c0048t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0015c0026t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0015c0026t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0016c0021t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0016c0021t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0016c0021t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0017c0028t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0018c0039t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0019c0038t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0020c0036t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0021c0040t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0022c0041t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0023c0032t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0024c0045t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0025c0049t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0026c0042t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| a0027c0031t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0159 | EUR | GBR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00140 | hp2 | a0004 | c0004 | t0001 | g0009 | EUR | GBR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0150 | EUR | FIN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0046 | EUR | FIN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00438 | hp1 | a0004 | c0004 | t0001 | g0126 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00438 | hp2 | a0001 | c0005 | t0001 | g0059 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00544 | hp1 | a0004 | c0004 | t0001 | g0113 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00544 | hp2 | a0004 | c0004 | t0001 | g0145 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0030 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00597 | hp1 | a0004 | c0004 | t0001 | g0119 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00621 | hp1 | a0004 | c0004 | t0001 | g0127 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00621 | hp2 | a0001 | c0012 | t0001 | g0017 | EAS | CHS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00639 | hp2 | a0015 | c0026 | t0001 | g0005 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00642 | hp1 | a0004 | c0004 | t0001 | g0080 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00738 | hp2 | a0002 | c0037 | t0001 | g0158 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01069 | hp1 | a0004 | c0008 | t0001 | g0161 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0252 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01070 | hp1 | a0015 | c0026 | t0001 | g0241 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01071 | hp1 | a0015 | c0026 | t0001 | g0005 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01071 | hp2 | a0004 | c0008 | t0001 | g0160 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0054 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01081 | hp1 | a0005 | c0006 | t0001 | g0274 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0095 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01099 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01109 | hp2 | a0008 | c0011 | t0001 | g0123 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0082 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0007 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0132 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01168 | hp2 | a0005 | c0006 | t0001 | g0285 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0122 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01175 | hp2 | a0005 | c0006 | t0001 | g0273 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01192 | hp1 | a0004 | c0004 | t0001 | g0129 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0153 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0032 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01243 | hp2 | a0009 | c0014 | t0001 | g0066 | AMR | PUR | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0286 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01255 | hp2 | a0002 | c0001 | t0002 | g0039 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01257 | hp2 | a0002 | c0001 | t0001 | g0036 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01258 | hp1 | a0002 | c0001 | t0001 | g0027 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0036 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01261 | hp1 | a0004 | c0004 | t0001 | g0169 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01346 | hp2 | a0014 | c0048 | t0001 | g0255 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01358 | hp1 | a0002 | c0001 | t0002 | g0039 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0010 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01361 | hp1 | a0001 | c0029 | t0001 | g0214 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01361 | hp2 | a0002 | c0001 | t0002 | g0037 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01496 | hp2 | a0002 | c0001 | t0002 | g0208 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0171 | EUR | IBS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0283 | EUR | IBS | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01884 | hp1 | a0006 | c0007 | t0001 | g0226 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01884 | hp2 | a0007 | c0009 | t0001 | g0243 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01891 | hp1 | a0004 | c0008 | t0001 | g0109 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01891 | hp2 | a0004 | c0004 | t0001 | g0154 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01934 | hp1 | a0002 | c0001 | t0002 | g0207 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01952 | hp2 | a0002 | c0001 | t0002 | g0206 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01978 | hp1 | a0009 | c0014 | t0001 | g0062 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0168 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01993 | hp2 | a0002 | c0001 | t0002 | g0211 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02027 | hp1 | a0002 | c0001 | t0001 | g0152 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0100 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02040 | hp1 | a0001 | c0005 | t0001 | g0057 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02040 | hp2 | a0004 | c0004 | t0001 | g0074 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02055 | hp1 | a0001 | c0022 | t0001 | g0174 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02055 | hp2 | a0001 | c0030 | t0001 | g0244 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02056 | hp1 | a0009 | c0014 | t0001 | g0060 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02071 | hp1 | a0002 | c0001 | t0002 | g0197 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02071 | hp2 | a0017 | c0028 | t0001 | g0003 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02074 | hp1 | a0017 | c0028 | t0001 | g0003 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02074 | hp2 | a0004 | c0004 | t0001 | g0144 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02080 | hp2 | a0001 | c0005 | t0001 | g0063 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02083 | hp2 | a0002 | c0001 | t0001 | g0114 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0131 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02132 | hp1 | a0001 | c0012 | t0001 | g0172 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0120 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02135 | hp1 | a0003 | c0003 | t0001 | g0110 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02135 | hp2 | a0004 | c0004 | t0001 | g0094 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02145 | hp1 | a0006 | c0007 | t0001 | g0293 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02145 | hp2 | a0011 | c0020 | t0001 | g0228 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0084 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02155 | hp2 | a0001 | c0012 | t0001 | g0017 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02165 | hp1 | a0001 | c0012 | t0001 | g0018 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CDX | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02257 | hp1 | a0007 | c0009 | t0001 | g0248 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02258 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02258 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0185 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02280 | hp1 | a0004 | c0008 | t0001 | g0151 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02280 | hp2 | a0004 | c0004 | t0001 | g0022 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02293 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PEL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02451 | hp1 | a0006 | c0007 | t0001 | g0229 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02451 | hp2 | a0007 | c0009 | t0001 | g0245 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02523 | hp1 | a0001 | c0012 | t0001 | g0056 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | KHV | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02572 | hp1 | a0010 | c0013 | t0001 | g0238 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02572 | hp2 | a0007 | c0009 | t0001 | g0246 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02602 | hp1 | a0001 | c0005 | t0001 | g0018 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02615 | hp1 | a0001 | c0024 | t0001 | g0182 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02615 | hp2 | a0010 | c0013 | t0001 | g0237 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02622 | hp1 | a0007 | c0009 | t0001 | g0042 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02622 | hp2 | a0010 | c0013 | t0001 | g0235 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02630 | hp1 | a0006 | c0007 | t0001 | g0225 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02630 | hp2 | a0018 | c0039 | t0001 | g0107 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02647 | hp1 | a0004 | c0034 | t0001 | g0149 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02647 | hp2 | a0013 | c0019 | t0001 | g0047 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02683 | hp1 | a0001 | c0005 | t0001 | g0003 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02683 | hp2 | a0004 | c0004 | t0001 | g0088 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02698 | hp1 | a0001 | c0030 | t0001 | g0089 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02698 | hp2 | a0020 | c0036 | t0001 | g0004 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02717 | hp1 | a0007 | c0009 | t0001 | g0042 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02717 | hp2 | a0004 | c0008 | t0001 | g0093 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02723 | hp1 | a0007 | c0009 | t0001 | g0247 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02723 | hp2 | a0013 | c0019 | t0001 | g0279 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0079 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02735 | hp2 | a0004 | c0004 | t0001 | g0009 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02738 | hp1 | a0014 | c0025 | t0001 | g0291 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02738 | hp2 | a0002 | c0001 | t0001 | g0072 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02809 | hp1 | a0016 | c0021 | t0001 | g0224 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02809 | hp2 | a0006 | c0010 | t0001 | g0041 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02818 | hp1 | a0001 | c0024 | t0001 | g0181 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02818 | hp2 | a0005 | c0015 | t0001 | g0179 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02886 | hp1 | a0005 | c0023 | t0001 | g0069 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02886 | hp2 | a0010 | c0013 | t0001 | g0234 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02895 | hp1 | a0011 | c0020 | t0001 | g0230 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02895 | hp2 | a0006 | c0010 | t0001 | g0040 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02896 | hp1 | a0006 | c0007 | t0001 | g0041 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02896 | hp2 | a0011 | c0027 | t0001 | g0220 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02897 | hp1 | a0006 | c0010 | t0001 | g0250 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02897 | hp2 | a0011 | c0027 | t0001 | g0223 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02922 | hp1 | a0011 | c0020 | t0001 | g0292 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02922 | hp2 | a0004 | c0008 | t0001 | g0108 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02965 | hp2 | a0008 | c0011 | t0001 | g0033 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02970 | hp1 | a0001 | c0022 | t0001 | g0070 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02970 | hp2 | a0002 | c0001 | t0001 | g0078 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02976 | hp1 | a0004 | c0004 | t0001 | g0073 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02976 | hp2 | a0001 | c0022 | t0001 | g0071 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03041 | hp1 | a0001 | c0024 | t0001 | g0180 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03041 | hp2 | a0006 | c0007 | t0001 | g0218 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03098 | hp1 | a0006 | c0010 | t0001 | g0040 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03098 | hp2 | a0004 | c0004 | t0001 | g0035 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03130 | hp1 | a0001 | c0018 | t0001 | g0281 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03130 | hp2 | a0006 | c0007 | t0001 | g0213 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03139 | hp1 | a0005 | c0015 | t0001 | g0299 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03139 | hp2 | a0001 | c0029 | t0001 | g0178 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03209 | hp1 | a0006 | c0007 | t0001 | g0216 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03209 | hp2 | a0005 | c0015 | t0001 | g0050 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03225 | hp1 | a0001 | c0018 | t0001 | g0043 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0028 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03239 | hp1 | a0005 | c0006 | t0001 | g0267 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03453 | hp1 | a0005 | c0023 | t0001 | g0067 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03486 | hp1 | a0016 | c0021 | t0001 | g0222 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03486 | hp2 | a0005 | c0033 | t0001 | g0236 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03491 | hp2 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03516 | hp1 | a0008 | c0011 | t0001 | g0166 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03516 | hp2 | a0023 | c0032 | t0001 | g0249 | AFR | ESN | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03540 | hp1 | a0005 | c0044 | t0001 | g0242 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03540 | hp2 | a0001 | c0018 | t0001 | g0043 | AFR | GWD | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03579 | hp1 | a0010 | c0013 | t0001 | g0239 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03579 | hp2 | a0005 | c0023 | t0001 | g0068 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03688 | hp2 | a0002 | c0001 | t0002 | g0199 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03704 | hp2 | a0002 | c0001 | t0002 | g0200 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03710 | hp1 | a0014 | c0025 | t0001 | g0002 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0118 | SAS | PJL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03831 | hp1 | a0001 | c0005 | t0001 | g0003 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03831 | hp2 | a0004 | c0004 | t0001 | g0031 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03834 | hp2 | a0004 | c0004 | t0001 | g0128 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03942 | hp1 | a0014 | c0025 | t0001 | g0272 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04115 | hp1 | a0004 | c0004 | t0001 | g0115 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04115 | hp2 | a0025 | c0049 | t0001 | g0257 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04184 | hp1 | a0005 | c0006 | t0001 | g0258 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04184 | hp2 | a0003 | c0003 | t0001 | g0157 | SAS | BEB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0007 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04204 | hp1 | a0004 | c0004 | t0001 | g0105 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04204 | hp2 | a0001 | c0050 | t0001 | g0013 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0276 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG04228 | hp2 | a0004 | c0004 | t0001 | g0102 | SAS | STU | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18522 | hp1 | a0004 | c0008 | t0001 | g0091 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18522 | hp2 | a0002 | c0001 | t0001 | g0121 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0096 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18612 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0087 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | CHB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18906 | hp2 | a0019 | c0038 | t0001 | g0022 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0081 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18939 | hp2 | a0002 | c0017 | t0001 | g0016 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18941 | hp1 | a0003 | c0003 | t0001 | g0133 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18941 | hp2 | a0005 | c0006 | t0002 | g0262 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18942 | hp1 | a0002 | c0001 | t0002 | g0205 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18948 | hp1 | a0001 | c0005 | t0001 | g0020 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18950 | hp1 | a0002 | c0001 | t0002 | g0196 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18950 | hp2 | a0022 | c0041 | t0002 | g0188 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18952 | hp1 | a0004 | c0004 | t0001 | g0097 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18953 | hp2 | a0002 | c0001 | t0002 | g0202 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18954 | hp2 | a0002 | c0017 | t0001 | g0138 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18963 | hp2 | a0002 | c0001 | t0002 | g0204 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18965 | hp2 | a0004 | c0004 | t0001 | g0175 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18966 | hp1 | a0001 | c0005 | t0001 | g0019 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18967 | hp1 | a0001 | c0005 | t0001 | g0058 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18967 | hp2 | a0002 | c0001 | t0002 | g0101 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18968 | hp2 | a0004 | c0004 | t0001 | g0190 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18969 | hp1 | a0004 | c0004 | t0001 | g0189 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18970 | hp1 | a0009 | c0047 | t0001 | g0266 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18970 | hp2 | a0004 | c0004 | t0001 | g0187 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18971 | hp1 | a0002 | c0001 | t0002 | g0038 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0027 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18978 | hp1 | a0005 | c0006 | t0001 | g0290 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18978 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18979 | hp2 | a0001 | c0005 | t0001 | g0019 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18982 | hp1 | a0001 | c0005 | t0001 | g0065 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18982 | hp2 | a0004 | c0004 | t0001 | g0051 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18983 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18983 | hp2 | a0004 | c0004 | t0001 | g0031 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18986 | hp2 | a0002 | c0001 | t0001 | g0116 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0164 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18991 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18992 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18993 | hp1 | a0021 | c0040 | t0002 | g0193 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18993 | hp2 | a0001 | c0005 | t0001 | g0021 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18995 | hp1 | a0002 | c0001 | t0002 | g0210 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18995 | hp2 | a0002 | c0001 | t0002 | g0186 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18999 | hp2 | a0012 | c0016 | t0001 | g0139 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19000 | hp1 | a0005 | c0006 | t0002 | g0240 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19000 | hp2 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19004 | hp1 | a0002 | c0001 | t0002 | g0201 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19004 | hp2 | a0004 | c0004 | t0001 | g0111 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19005 | hp1 | a0001 | c0005 | t0001 | g0020 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19005 | hp2 | a0002 | c0017 | t0001 | g0016 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19006 | hp1 | a0005 | c0006 | t0002 | g0268 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19006 | hp2 | a0001 | c0005 | t0001 | g0173 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19007 | hp1 | a0027 | c0031 | t0001 | g0142 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19007 | hp2 | a0004 | c0004 | t0001 | g0141 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19009 | hp1 | a0005 | c0006 | t0002 | g0261 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19011 | hp2 | a0001 | c0005 | t0001 | g0061 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19012 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19030 | hp1 | a0004 | c0035 | t0001 | g0183 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19030 | hp2 | a0008 | c0011 | t0001 | g0001 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19043 | hp1 | a0006 | c0007 | t0001 | g0219 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19043 | hp2 | a0008 | c0011 | t0001 | g0033 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19054 | hp1 | a0026 | c0042 | t0002 | g0195 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19055 | hp2 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0212 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19056 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19057 | hp1 | a0002 | c0001 | t0002 | g0038 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19058 | hp1 | a0005 | c0006 | t0001 | g0265 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19058 | hp2 | a0002 | c0001 | t0002 | g0198 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0124 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19063 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19064 | hp1 | a0007 | c0043 | t0001 | g0012 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19067 | hp1 | a0002 | c0017 | t0001 | g0055 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19068 | hp1 | a0001 | c0005 | t0001 | g0003 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19072 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0130 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19074 | hp2 | a0002 | c0001 | t0002 | g0209 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19075 | hp1 | a0002 | c0001 | t0002 | g0194 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19075 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19076 | hp1 | a0004 | c0004 | t0001 | g0176 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19077 | hp1 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19077 | hp2 | a0002 | c0001 | t0002 | g0192 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19078 | hp1 | a0004 | c0004 | t0001 | g0106 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19082 | hp1 | a0002 | c0001 | t0002 | g0191 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19082 | hp2 | a0004 | c0004 | t0001 | g0135 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0287 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19083 | hp2 | a0002 | c0001 | t0002 | g0052 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19084 | hp1 | a0002 | c0001 | t0002 | g0184 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19085 | hp1 | a0012 | c0016 | t0001 | g0137 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19087 | hp1 | a0012 | c0016 | t0001 | g0136 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19090 | hp1 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19090 | hp2 | a0001 | c0005 | t0001 | g0021 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19091 | hp1 | a0012 | c0016 | t0001 | g0140 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19091 | hp2 | a0024 | c0045 | t0001 | g0045 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19240 | hp1 | a0006 | c0007 | t0001 | g0217 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA19240 | hp2 | a0013 | c0019 | t0001 | g0280 | AFR | YRI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | ASW | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20129 | hp2 | a0016 | c0021 | t0001 | g0221 | AFR | ASW | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20805 | hp1 | a0004 | c0004 | t0001 | g0009 | EUR | TSI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20805 | hp2 | a0002 | c0001 | t0001 | g0032 | EUR | TSI | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | GIH | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0296 | SAS | GIH | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG01123 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | CLM | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02109 | hp1 | a0009 | c0014 | t0001 | g0064 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02109 | hp2 | a0001 | c0018 | t0001 | g0259 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0028 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02486 | hp2 | a0005 | c0015 | t0001 | g0177 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02559 | hp1 | a0001 | c0046 | t0001 | g0288 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG02559 | hp2 | a0006 | c0010 | t0001 | g0227 | AFR | ACB | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03471 | hp1 | a0013 | c0019 | t0001 | g0047 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG03471 | hp2 | a0006 | c0010 | t0001 | g0215 | AFR | MSL | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG06807 | hp1 | a0004 | c0008 | t0001 | g0092 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18955 | hp1 | a0004 | c0004 | t0001 | g0203 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0077 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA20300 | hp2 | a0002 | c0001 | t0002 | g0037 | AFR | USA | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA21309 | hp1 | a0008 | c0011 | t0001 | g0076 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | LWK | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0001 | REF | REF | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| homoSapiens_grch38 | hp1 | a0004 | c0004 | t0001 | g0035 | REF | REF | HELB_chr12_66297493_66343199 | HELB | chr12 | 66297493 | 66343199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:66302684
|
C | A | 1 | a0027 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.81C>A | p.Asp27Glu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/13 | 192/3472 | 81/3264 | 27/1087 | chr12 | 66302684 | ||
| chr12:66304989
|
A | G | 1 | a0026 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.446A>G | p.Lys149Arg | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/13 | 557/3472 | 446/3264 | 149/1087 | chr12 | 66304989 | ||
| chr12:66305057
|
G | A | 3 | a0006a0011a0016 | 24 | HG01884.hp1 HG02145.hp1 HG02145.hp2 others(21): Show |
missense_variant | MODERATE | c.514G>A | p.Glu172Lys | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/13 | 625/3472 | 514/3264 | 172/1087 | chr12 | 66305057 | ||
| chr12:66305115
|
T | C | 15 | a0001a0005a0006others(12): Show | 179 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(176): Show |
missense_variant | MODERATE | c.572T>C | p.Leu191Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/13 | 683/3472 | 572/3264 | 191/1087 | chr12 | 66305115 | ||
| chr12:66309727
|
C | T | 1 | a0008 | 6 | HG01109.hp2 HG02965.hp2 HG03516.hp1 others(3): Show |
missense_variant | MODERATE | c.799C>T | p.Leu267Phe | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 910/3472 | 799/3264 | 267/1087 | chr12 | 66309727 | ||
| chr12:66310388
|
G | A | 2 | a0007a0023 | 9 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.1460G>A | p.Arg487His | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1571/3472 | 1460/3264 | 487/1087 | chr12 | 66310388 | ||
| chr12:66310445
|
A | G | 3 | a0014a0015a0025 | 8 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
missense_variant | MODERATE | c.1517A>G | p.Asp506Gly | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1628/3472 | 1517/3264 | 506/1087 | chr12 | 66310445 | ||
| chr12:66310496
|
A | C | 1 | a0015 | 3 | HG00639.hp2 HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.1568A>C | p.Gln523Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1679/3472 | 1568/3264 | 523/1087 | chr12 | 66310496 | ||
| chr12:66314028
|
A | G | 1 | a0013 | 4 | HG02647.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.1723A>G | p.Thr575Ala | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/13 | 1834/3472 | 1723/3264 | 575/1087 | chr12 | 66314028 | ||
| chr12:66315325
|
A | G | 4 | a0010a0016a0021others(1): Show | 10 | HG02572.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
missense_variant | MODERATE | c.1942A>G | p.Ile648Val | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/13 | 2053/3472 | 1942/3264 | 648/1087 | chr12 | 66315325 | ||
| chr12:66318648
|
C | T | 1 | a0018 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2011C>T | p.Arg671Cys | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/13 | 2122/3472 | 2011/3264 | 671/1087 | chr12 | 66318648 | ||
| chr12:66322010
|
C | T | 1 | a0017 | 2 | HG02071.hp2 HG02074.hp1 |
stop_gained | HIGH | c.2218C>T | p.Gln740* | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/13 | 2329/3472 | 2218/3264 | 740/1087 | chr12 | 66322010 | ||
| chr12:66322762
|
A | T | 1 | a0022 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.2276A>T | p.His759Leu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/13 | 2387/3472 | 2276/3264 | 759/1087 | chr12 | 66322762 | ||
| chr12:66324176
|
C | T | 1 | a0019 | 1 | NA18906.hp2 | stop_gained | HIGH | c.2491C>T | p.Arg831* | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2602/3472 | 2491/3264 | 831/1087 | chr12 | 66324176 | ||
| chr12:66331160
|
G | A | 1 | a0024 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.2677G>A | p.Glu893Lys | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2788/3472 | 2677/3264 | 893/1087 | chr12 | 66331160 | ||
| chr12:66331320
|
G | A | 1 | a0012 | 4 | NA18999.hp2 NA19085.hp1 NA19087.hp1 others(1): Show |
missense_variant | MODERATE | c.2837G>A | p.Arg946His | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2948/3472 | 2837/3264 | 946/1087 | chr12 | 66331320 | ||
| chr12:66331373
|
G | T | 1 | a0020 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2890G>T | p.Asp964Tyr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3001/3472 | 2890/3264 | 964/1087 | chr12 | 66331373 | ||
| chr12:66331380
|
C | T | 17 | a0002a0003a0005others(14): Show | 201 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(198): Show |
missense_variant | MODERATE | c.2897C>T | p.Pro966Leu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3008/3472 | 2897/3264 | 966/1087 | chr12 | 66331380 | ||
| chr12:66331422
|
C | T | 8 | a0003a0009a0012others(5): Show | 65 | HG00280.hp1 HG00558.hp2 HG00597.hp2 others(62): Show |
missense_variant | MODERATE | c.2939C>T | p.Thr980Ile | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3050/3472 | 2939/3264 | 980/1087 | chr12 | 66331422 | ||
| chr12:66331521
|
T | C | 1 | a0013 | 4 | HG02647.hp2 HG02723.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.3038T>C | p.Phe1013Ser | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3149/3472 | 3038/3264 | 1013/1087 | chr12 | 66331521 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:66302630
|
C | T | 14 | a0001c0002a0001c0018a0001c0046others(11): Show | 94 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(91): Show |
synonymous_variant | LOW | c.27C>T | p.Arg9Arg | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/13 | 138/3472 | 27/3264 | 9/1087 | chr12 | 66302630 | ||
| chr12:66306493
|
G | A | 6 | a0001c0005a0001c0012a0001c0022others(3): Show | 36 | HG00438.hp2 HG00621.hp2 HG01243.hp2 others(33): Show |
synonymous_variant | LOW | c.756G>A | p.Pro252Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/13 | 867/3472 | 756/3264 | 252/1087 | chr12 | 66306493 | ||
| chr12:66309963
|
A | T | 1 | a0001c0050 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1035A>T | p.Thr345Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/13 | 1146/3472 | 1035/3264 | 345/1087 | chr12 | 66309963 | ||
| chr12:66324004
|
T | A | 12 | a0001c0005a0001c0012a0001c0022others(9): Show | 54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
synonymous_variant | LOW | c.2319T>A | p.Val773Val | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2430/3472 | 2319/3264 | 773/1087 | chr12 | 66324004 | ||
| chr12:66324130
|
G | A | 1 | a0014c0048 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.2445G>A | p.Thr815Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2556/3472 | 2445/3264 | 815/1087 | chr12 | 66324130 | ||
| chr12:66324130
|
G | T | 12 | a0001c0005a0001c0012a0001c0022others(9): Show | 54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
synonymous_variant | LOW | c.2445G>T | p.Thr815Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/13 | 2556/3472 | 2445/3264 | 815/1087 | chr12 | 66324130 | ||
| chr12:66331336
|
G | A | 1 | a0001c0012 | 5 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(2): Show |
synonymous_variant | LOW | c.2853G>A | p.Leu951Leu | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2964/3472 | 2853/3264 | 951/1087 | chr12 | 66331336 | ||
| chr12:66331357
|
C | T | 1 | a0002c0037 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.2874C>T | p.Ser958Ser | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 2985/3472 | 2874/3264 | 958/1087 | chr12 | 66331357 | ||
| chr12:66331426
|
G | A | 1 | a0002c0017 | 4 | NA18939.hp2 NA18954.hp2 NA19005.hp2 others(1): Show |
synonymous_variant | LOW | c.2943G>A | p.Pro981Pro | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3054/3472 | 2943/3264 | 981/1087 | chr12 | 66331426 | ||
| chr12:66331486
|
C | T | 1 | a0004c0035 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.3003C>T | p.Ser1001Ser | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3114/3472 | 3003/3264 | 1001/1087 | chr12 | 66331486 | ||
| chr12:66331612
|
G | A | 1 | a0001c0018 | 4 | HG02109.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.3129G>A | p.Val1043Val | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/13 | 3240/3472 | 3129/3264 | 1043/1087 | chr12 | 66331612 | ||
| chr12:66338084
|
C | A | 32 | a0001c0022a0001c0024a0001c0046others(29): Show | 227 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(224): Show |
synonymous_variant | LOW | c.3246C>A | p.Thr1082Thr | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 13/13 | 3357/3472 | 3246/3264 | 1082/1087 | chr12 | 66338084 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:66338132
|
GT | G | 6 | a0002c0001t0002a0003c0003t0002a0005c0006t0002others(3): Show | 37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*35delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 13/13 | 35 | INFO_REALIGN_3_PRIME | chr12 | 66338132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:66302902
|
A | G | 1 | a0005c0015t0001g0299 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.187+112A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302902 | ||||||
| chr12:66302903
|
G | A | 1 | a0005c0015t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+113G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302903 | ||||||
| chr12:66302926
|
C | T | 149 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(146): Show | 178 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(175): Show |
intron_variant | MODIFIER | c.187+136C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302926 | ||||||
| chr12:66302985
|
G | GT | 13 | a0001c0002t0001g0049a0001c0002t0001g0294a0001c0002t0001g0295others(10): Show | 14 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.187+210dupT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66302985 | |||||
| chr12:66302985
|
GT | G | 16 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(13): Show | 18 | HG01074.hp2 HG02486.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.187+210delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66302985 | |||||
| chr12:66302989
|
T | G | 9 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(6): Show | 9 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+199T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66302989 | ||||||
| chr12:66303086
|
CT | C | 45 | a0001c0029t0001g0178a0002c0001t0001g0081a0002c0001t0001g0086others(42): Show | 48 | HG01167.hp1 HG01255.hp2 HG01358.hp1 others(45): Show |
intron_variant | MODIFIER | c.187+317delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303086 | |||||
| chr12:66303086
|
CTT | C | 12 | a0001c0029t0001g0214a0006c0007t0001g0213a0006c0007t0001g0216others(9): Show | 12 | HG01361.hp1 HG02809.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.187+316_187+317del others(2): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303086 | |||||
| chr12:66303101
|
T | A | 3 | a0001c0012t0001g0017a0001c0012t0001g0056a0001c0012t0001g0172 | 4 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+311T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303101 | ||||||
| chr12:66303102
|
T | A | 12 | a0001c0005t0001g0018a0001c0012t0001g0017a0001c0012t0001g0018others(9): Show | 13 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.187+312T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303102 | ||||||
| chr12:66303103
|
T | A | 61 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(58): Show | 73 | HG00438.hp2 HG00621.hp2 HG01255.hp2 others(70): Show |
intron_variant | MODIFIER | c.187+313T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303103 | ||||||
| chr12:66303104
|
T | A | 67 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(64): Show | 79 | HG00438.hp2 HG00621.hp2 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.187+314T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303104 | ||||||
| chr12:66303105
|
T | A | 69 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(66): Show | 81 | HG00438.hp2 HG00621.hp2 HG01243.hp2 others(78): Show |
intron_variant | MODIFIER | c.187+315T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303105 | ||||||
| chr12:66303105
|
TTTA | T | 6 | a0006c0007t0001g0041a0006c0007t0001g0225a0006c0007t0001g0226others(3): Show | 7 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+316_187+318del others(3): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303105 | ||||||
| chr12:66303106
|
T | A | 80 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(77): Show | 92 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.187+316T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303106 | ||||||
| chr12:66303106
|
TTA | T | 20 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0001g0233others(17): Show | 21 | HG01070.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.187+317_187+318del others(2): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303106 | ||||||
| chr12:66303107
|
T | A | 205 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(202): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.187+317T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303107 | ||||||
| chr12:66303107
|
T | TA | 3 | a0002c0017t0001g0055a0003c0003t0001g0162a0003c0003t0001g0163 | 3 | NA18978.hp2 NA19009.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.187+321dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303107 | |||||
| chr12:66303107
|
TA | T | 60 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(57): Show | 84 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.187+321delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66303107 | |||||
| chr12:66303108
|
A | T | 4 | a0001c0002t0001g0289a0001c0002t0001g0298a0005c0006t0001g0290others(1): Show | 4 | HG01109.hp1 HG01261.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+318A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303108 | ||||||
| chr12:66303620
|
T | C | 176 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(173): Show | 214 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.187+830T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303620 | ||||||
| chr12:66303889
|
T | C | 1 | a0002c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.188-842T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303889 | ||||||
| chr12:66303900
|
T | C | 5 | a0006c0007t0001g0229a0006c0007t0001g0293a0011c0020t0001g0228others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-831T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66303900 | ||||||
| chr12:66304008
|
A | G | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.188-723A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304008 | ||||||
| chr12:66304024
|
C | T | 3 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182 | 3 | HG02615.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.188-707C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304024 | ||||||
| chr12:66304065
|
A | G | 1 | a0001c0002t0001g0049 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.188-666A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304065 | ||||||
| chr12:66304295
|
T | G | 2 | a0001c0002t0001g0251a0001c0002t0001g0252 | 2 | HG01069.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.188-436T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304295 | ||||||
| chr12:66304296
|
GAT | G | 86 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(83): Show | 111 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.188-433_188-432del others(2): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66304296 | |||||
| chr12:66304364
|
A | G | 136 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(133): Show | 171 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.188-367A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304364 | ||||||
| chr12:66304658
|
G | A | 176 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(173): Show | 214 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.188-73G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304658 | ||||||
| chr12:66304681
|
A | G | 136 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(133): Show | 171 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.188-50A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304681 | ||||||
| chr12:66304700
|
C | T | 1 | a0002c0001t0002g0039 | 2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.188-31C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | chr12 | 66304700 | ||||||
| chr12:66304719
|
GT | G | 8 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.188-3delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 66304719 | |||||
| chr12:66305174
|
C | G | 201 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(198): Show | 247 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.607+24C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305174 | ||||||
| chr12:66305314
|
T | C | 1 | a0006c0010t0001g0215 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.607+164T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305314 | ||||||
| chr12:66305380
|
C | T | 176 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(173): Show | 214 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.607+230C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305380 | ||||||
| chr12:66305511
|
G | A | 32 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(29): Show | 35 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.607+361G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305511 | ||||||
| chr12:66305746
|
TA | T | 160 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(157): Show | 203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.608-584delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 66305746 | |||||
| chr12:66305782
|
T | A | 4 | a0004c0008t0001g0091a0004c0008t0001g0092a0004c0008t0001g0093others(1): Show | 4 | HG02280.hp1 HG02717.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-563T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305782 | ||||||
| chr12:66305790
|
G | A | 1 | a0002c0001t0001g0079 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.608-555G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305790 | ||||||
| chr12:66305974
|
G | A | 1 | a0006c0007t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.608-371G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66305974 | ||||||
| chr12:66306087
|
A | C | 8 | a0001c0030t0001g0244a0007c0009t0001g0042a0007c0009t0001g0243others(5): Show | 9 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-258A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66306087 | ||||||
| chr12:66306142
|
G | T | 160 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(157): Show | 203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.608-203G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66306142 | ||||||
| chr12:66306324
|
T | C | 7 | a0002c0001t0001g0023a0002c0001t0001g0024a0002c0001t0001g0025others(4): Show | 10 | HG01099.hp1 HG02135.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.608-21T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 2/12 | chr12 | 66306324 | ||||||
| chr12:66306592
|
T | C | 3 | a0004c0004t0001g0022a0004c0004t0001g0073a0019c0038t0001g0022 | 3 | HG02280.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.777+78T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306592 | ||||||
| chr12:66306928
|
C | T | 1 | a0001c0002t0001g0287 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.777+414C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306928 | ||||||
| chr12:66306942
|
C | T | 1 | a0001c0002t0001g0286 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.777+428C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306942 | ||||||
| chr12:66306950
|
A | G | 1 | a0003c0003t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.777+436A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66306950 | ||||||
| chr12:66307221
|
A | G | 134 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(131): Show | 168 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.777+707A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307221 | ||||||
| chr12:66307300
|
A | G | 1 | a0001c0029t0001g0214 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.777+786A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307300 | ||||||
| chr12:66307376
|
T | TA | 19 | a0002c0001t0001g0015a0002c0001t0001g0027a0002c0001t0001g0053others(16): Show | 23 | HG01258.hp1 HG02027.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.777+869dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66307376 | |||||
| chr12:66307767
|
T | C | 111 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(108): Show | 144 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.777+1253T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307767 | ||||||
| chr12:66307797
|
G | T | 168 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(165): Show | 211 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.777+1283G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307797 | ||||||
| chr12:66307844
|
G | A | 1 | a0002c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.777+1330G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307844 | ||||||
| chr12:66307948
|
A | C | 201 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(198): Show | 247 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.777+1434A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66307948 | ||||||
| chr12:66308043
|
T | TA | 30 | a0001c0002t0001g0252a0001c0002t0001g0283a0001c0002t0001g0284others(27): Show | 32 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.777+1551dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | |||||
| chr12:66308043
|
T | TAA | 127 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(124): Show | 169 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.777+1550_777+1551d others(4): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | |||||
| chr12:66308043
|
T | TAAA | 10 | a0001c0002t0001g0254a0002c0001t0001g0034a0002c0001t0001g0087others(7): Show | 11 | HG01192.hp2 HG01346.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.777+1549_777+1551d others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | |||||
| chr12:66308043
|
TA | T | 13 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(10): Show | 14 | HG02486.hp2 HG02615.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.777+1551delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 66308043 | |||||
| chr12:66308070
|
A | G | 1 | a0001c0002t0001g0048 | 2 | HG02293.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.777+1556A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308070 | ||||||
| chr12:66308102
|
T | A | 1 | a0003c0003t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.777+1588T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308102 | ||||||
| chr12:66308102
|
T | G | 160 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(157): Show | 203 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.777+1588T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308102 | ||||||
| chr12:66308183
|
C | T | 1 | a0001c0024t0001g0182 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.778-1523C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308183 | ||||||
| chr12:66308203
|
A | T | 6 | a0006c0007t0001g0041a0006c0007t0001g0225a0006c0010t0001g0040others(3): Show | 7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-1503A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308203 | ||||||
| chr12:66308296
|
T | A | 1 | a0001c0002t0001g0256 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.778-1410T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308296 | ||||||
| chr12:66308348
|
G | A | 1 | a0003c0003t0001g0010 | 3 | HG01358.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.778-1358G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308348 | ||||||
| chr12:66308378
|
A | T | 201 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(198): Show | 247 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(244): Show |
intron_variant | MODIFIER | c.778-1328A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308378 | ||||||
| chr12:66308647
|
G | C | 1 | a0025c0049t0001g0257 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.778-1059G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66308647 | ||||||
| chr12:66309060
|
G | T | 1 | a0001c0002t0001g0282 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.778-646G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66309060 | ||||||
| chr12:66309204
|
C | T | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.778-502C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 3/12 | chr12 | 66309204 | ||||||
| chr12:66310621
|
A | G | 3 | a0011c0020t0001g0228a0011c0020t0001g0230a0011c0020t0001g0292 | 3 | HG02145.hp2 HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1680+13A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310621 | ||||||
| chr12:66310727
|
T | C | 1 | a0007c0009t0001g0243 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1680+119T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310727 | ||||||
| chr12:66310811
|
A | G | 205 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(202): Show | 251 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.1680+203A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310811 | ||||||
| chr12:66310818
|
C | G | 1 | a0001c0018t0001g0281 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1680+210C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310818 | ||||||
| chr12:66310828
|
G | A | 1 | a0001c0005t0001g0019 | 2 | NA18966.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1680+220G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310828 | ||||||
| chr12:66310846
|
A | G | 34 | a0001c0029t0001g0178a0002c0001t0002g0037a0002c0001t0002g0038others(31): Show | 37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.1680+238A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310846 | ||||||
| chr12:66310916
|
C | T | 1 | a0002c0001t0002g0186 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1680+308C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310916 | ||||||
| chr12:66310917
|
G | A | 124 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(121): Show | 156 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.1680+309G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66310917 | ||||||
| chr12:66311036
|
G | A | 157 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(154): Show | 193 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.1680+428G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311036 | ||||||
| chr12:66311086
|
G | C | 2 | a0001c0002t0001g0251a0001c0002t0001g0252 | 2 | HG01069.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1680+478G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311086 | ||||||
| chr12:66311088
|
T | A | 7 | a0001c0029t0001g0214a0004c0008t0001g0091a0004c0008t0001g0092others(4): Show | 7 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1680+480T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311088 | ||||||
| chr12:66311149
|
G | A | 3 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182 | 3 | HG02615.hp1 HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1680+541G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311149 | ||||||
| chr12:66311157
|
G | GA | 140 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(137): Show | 175 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.1680+563dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 66311157 | |||||
| chr12:66311202
|
T | G | 6 | a0004c0008t0001g0091a0004c0008t0001g0092a0004c0008t0001g0093others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1680+594T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311202 | ||||||
| chr12:66311332
|
T | C | 5 | a0006c0007t0001g0229a0006c0007t0001g0293a0011c0020t0001g0228others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1680+724T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311332 | ||||||
| chr12:66311817
|
G | C | 7 | a0001c0029t0001g0214a0004c0008t0001g0091a0004c0008t0001g0092others(4): Show | 7 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1680+1209G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311817 | ||||||
| chr12:66311860
|
A | C | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1680+1252A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66311860 | ||||||
| chr12:66312028
|
G | T | 34 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(31): Show | 43 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.1680+1420G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312028 | ||||||
| chr12:66312144
|
A | G | 1 | a0001c0005t0001g0063 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1680+1536A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312144 | ||||||
| chr12:66312173
|
AG | A | 15 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(12): Show | 18 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.1680+1566delG | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312173 | ||||||
| chr12:66312203
|
A | G | 1 | a0002c0001t0001g0032 | 2 | HG01243.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1680+1595A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312203 | ||||||
| chr12:66312246
|
G | A | 199 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(196): Show | 244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.1680+1638G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312246 | ||||||
| chr12:66312306
|
G | T | 145 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(142): Show | 180 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.1681-1680G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312306 | ||||||
| chr12:66312779
|
T | G | 309 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(306): Show | 388 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1681-1207T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312779 | ||||||
| chr12:66312968
|
T | G | 198 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(195): Show | 243 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.1681-1018T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312968 | ||||||
| chr12:66312990
|
T | C | 8 | a0001c0029t0001g0214a0004c0008t0001g0091a0004c0008t0001g0092others(5): Show | 8 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1681-996T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66312990 | ||||||
| chr12:66313114
|
C | A | 2 | a0003c0003t0001g0112a0004c0004t0001g0111 | 2 | NA19004.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1681-872C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313114 | ||||||
| chr12:66313200
|
T | TAGAAAAA others(3): Show |
116 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(113): Show | 148 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(145): Show |
intron_variant | MODIFIER | c.1681-779_1681-778i others(12): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 66313200 | |||||
| chr12:66313380
|
C | T | 3 | a0001c0012t0001g0017a0001c0012t0001g0056a0001c0012t0001g0172 | 4 | HG00621.hp2 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.1681-606C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313380 | ||||||
| chr12:66313543
|
C | T | 7 | a0002c0001t0001g0023a0002c0001t0001g0024a0002c0001t0001g0025others(4): Show | 10 | HG01099.hp1 HG02135.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1681-443C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313543 | ||||||
| chr12:66313619
|
G | A | 2 | a0003c0003t0001g0028a0003c0003t0001g0082 | 3 | HG01167.hp1 HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1681-367G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313619 | ||||||
| chr12:66313864
|
G | T | 47 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(44): Show | 56 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(53): Show |
intron_variant | MODIFIER | c.1681-122G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313864 | ||||||
| chr12:66313949
|
A | T | 2 | a0002c0001t0002g0184a0002c0001t0002g0201 | 2 | NA19004.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1681-37A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313949 | ||||||
| chr12:66313973
|
A | G | 5 | a0006c0007t0001g0229a0006c0007t0001g0293a0011c0020t0001g0228others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1681-13A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 4/12 | chr12 | 66313973 | ||||||
| chr12:66314213
|
GTTAGTTG others(14): Show |
G | 29 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(26): Show | 32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.1858+71_1858+91del others(21): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 66314213 | |||||
| chr12:66314284
|
C | T | 7 | a0001c0046t0001g0288a0007c0009t0001g0042a0007c0009t0001g0243others(4): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1858+121C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314284 | ||||||
| chr12:66314358
|
T | A | 199 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(196): Show | 244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.1858+195T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314358 | ||||||
| chr12:66314727
|
G | C | 48 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(45): Show | 57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.1859-515G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314727 | ||||||
| chr12:66314976
|
A | G | 1 | a0003c0003t0001g0146 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1859-266A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66314976 | ||||||
| chr12:66315004
|
C | T | 289 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(286): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.1859-238C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 5/12 | chr12 | 66315004 | ||||||
| chr12:66315573
|
T | C | 199 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(196): Show | 244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2000+190T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315573 | ||||||
| chr12:66315654
|
T | A | 6 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+271T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315654 | ||||||
| chr12:66315708
|
C | T | 40 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(37): Show | 49 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.2000+325C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315708 | ||||||
| chr12:66315751
|
G | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+368G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315751 | ||||||
| chr12:66315792
|
C | T | 65 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(62): Show | 88 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.2000+409C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315792 | ||||||
| chr12:66315904
|
C | T | 7 | a0001c0046t0001g0288a0007c0009t0001g0042a0007c0009t0001g0243others(4): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000+521C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315904 | ||||||
| chr12:66315968
|
T | C | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+585T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315968 | ||||||
| chr12:66315987
|
G | A | 1 | a0001c0002t0001g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2000+604G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66315987 | ||||||
| chr12:66316183
|
C | T | 8 | a0001c0029t0001g0214a0004c0008t0001g0091a0004c0008t0001g0092others(5): Show | 8 | HG01361.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+800C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316183 | ||||||
| chr12:66316258
|
G | A | 1 | a0009c0014t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2000+875G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316258 | ||||||
| chr12:66316330
|
A | G | 1 | a0006c0007t0001g0293 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2000+947A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316330 | ||||||
| chr12:66316344
|
T | A | 1 | a0006c0007t0001g0293 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2000+961T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316344 | ||||||
| chr12:66316421
|
G | A | 5 | a0006c0007t0001g0229a0006c0007t0001g0293a0011c0020t0001g0228others(2): Show | 5 | HG02145.hp1 HG02145.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2000+1038G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316421 | ||||||
| chr12:66316567
|
A | AAAT | 8 | a0001c0005t0001g0020a0002c0001t0001g0025a0003c0003t0001g0085others(5): Show | 10 | HG00544.hp2 HG02015.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2000+1217_2000+121 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
A | AAATAAT | 72 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(69): Show | 83 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(80): Show |
intron_variant | MODIFIER | c.2000+1214_2000+121 others(10): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
A | AAATAATA others(2): Show |
20 | a0001c0029t0001g0178a0001c0029t0001g0214a0004c0034t0001g0149others(17): Show | 22 | HG01361.hp1 HG01884.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2000+1211_2000+121 others(13): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
A | AAATAATA others(5): Show |
12 | a0001c0022t0001g0070a0001c0022t0001g0174a0001c0030t0001g0244others(9): Show | 12 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2000+1208_2000+121 others(16): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
A | AAATAATA others(8): Show |
3 | a0001c0022t0001g0071a0001c0046t0001g0288a0010c0013t0001g0238 | 3 | HG02559.hp1 HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2000+1205_2000+121 others(19): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
A | AAATAATA others(11): Show |
1 | a0010c0013t0001g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2000+1202_2000+121 others(22): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
AAAT | A | 60 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(57): Show | 83 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.2000+1217_2000+121 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
AAATAAT | A | 32 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0001g0233others(29): Show | 41 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.2000+1214_2000+121 others(10): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316567
|
AAATAATA others(5): Show |
A | 5 | a0001c0002t0001g0289a0001c0002t0001g0294a0001c0002t0001g0295others(2): Show | 5 | HG00741.hp1 HG01109.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.2000+1208_2000+121 others(16): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66316567 | |||||
| chr12:66316619
|
C | T | 1 | a0027c0031t0001g0142 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2000+1236C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316619 | ||||||
| chr12:66316741
|
C | T | 6 | a0006c0007t0001g0041a0006c0007t0001g0225a0006c0010t0001g0040others(3): Show | 7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+1358C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316741 | ||||||
| chr12:66316748
|
G | A | 7 | a0001c0046t0001g0288a0007c0009t0001g0042a0007c0009t0001g0243others(4): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2000+1365G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316748 | ||||||
| chr12:66316757
|
T | G | 2 | a0001c0029t0001g0178a0005c0015t0001g0177 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2000+1374T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316757 | ||||||
| chr12:66316816
|
G | A | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+1433G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316816 | ||||||
| chr12:66316887
|
C | T | 1 | a0001c0002t0001g0233 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2000+1504C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316887 | ||||||
| chr12:66316892
|
G | A | 48 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(45): Show | 57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2000+1509G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316892 | ||||||
| chr12:66316897
|
T | C | 29 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(26): Show | 32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2000+1514T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316897 | ||||||
| chr12:66316950
|
C | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2000+1567C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316950 | ||||||
| chr12:66316967
|
C | T | 2 | a0002c0001t0001g0024a0002c0001t0001g0081 | 3 | NA18939.hp1 NA19063.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2000+1584C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66316967 | ||||||
| chr12:66317018
|
C | CA | 10 | a0003c0003t0001g0030a0003c0003t0001g0110a0003c0003t0001g0122others(7): Show | 12 | HG00558.hp2 HG01175.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2001-1599dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317018 | |||||
| chr12:66317018
|
CA | C | 141 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(138): Show | 173 | HG00140.hp1 HG00558.hp1 HG00639.hp1 others(170): Show |
intron_variant | MODIFIER | c.2001-1599delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317018 | |||||
| chr12:66317018
|
CAA | C | 52 | a0001c0002t0001g0046a0001c0002t0001g0277a0001c0002t0001g0278others(49): Show | 64 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.2001-1600_2001-159 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317018 | |||||
| chr12:66317101
|
A | G | 199 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(196): Show | 244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2001-1537A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317101 | ||||||
| chr12:66317111
|
C | T | 28 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(25): Show | 31 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2001-1527C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317111 | ||||||
| chr12:66317185
|
C | T | 2 | a0005c0015t0001g0050a0005c0015t0001g0299 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2001-1453C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317185 | ||||||
| chr12:66317196
|
C | CA | 29 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0034others(26): Show | 38 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.2001-1430dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317196 | |||||
| chr12:66317196
|
CA | C | 10 | a0003c0003t0001g0147a0004c0004t0001g0176a0006c0007t0001g0041others(7): Show | 11 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2001-1430delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 66317196 | |||||
| chr12:66317311
|
A | G | 2 | a0001c0022t0001g0070a0001c0022t0001g0071 | 2 | HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2001-1327A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317311 | ||||||
| chr12:66317455
|
A | T | 199 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(196): Show | 244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2001-1183A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317455 | ||||||
| chr12:66317562
|
C | T | 1 | a0005c0033t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2001-1076C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317562 | ||||||
| chr12:66317677
|
G | A | 206 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(203): Show | 252 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.2001-961G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317677 | ||||||
| chr12:66317720
|
C | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2001-918C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317720 | ||||||
| chr12:66317721
|
G | T | 2 | a0002c0001t0002g0199a0002c0001t0002g0200 | 2 | HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2001-917G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317721 | ||||||
| chr12:66317814
|
C | A | 1 | a0008c0011t0001g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2001-824C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317814 | ||||||
| chr12:66317933
|
G | A | 1 | a0002c0001t0001g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2001-705G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66317933 | ||||||
| chr12:66318096
|
C | T | 22 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(19): Show | 22 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2001-542C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318096 | ||||||
| chr12:66318097
|
A | G | 3 | a0002c0001t0001g0029a0002c0001t0001g0054a0002c0001t0001g0121 | 4 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001-541A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318097 | ||||||
| chr12:66318115
|
A | G | 48 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(45): Show | 57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2001-523A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318115 | ||||||
| chr12:66318564
|
A | T | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2001-74A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 6/12 | chr12 | 66318564 | ||||||
| chr12:66318872
|
C | T | 48 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(45): Show | 57 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2155+80C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66318872 | ||||||
| chr12:66318940
|
G | T | 90 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(87): Show | 121 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.2155+148G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66318940 | ||||||
| chr12:66319101
|
C | A | 1 | a0007c0009t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2155+309C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319101 | ||||||
| chr12:66319110
|
T | C | 6 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155+318T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319110 | ||||||
| chr12:66319167
|
A | T | 1 | a0006c0007t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2155+375A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319167 | ||||||
| chr12:66319280
|
C | A | 199 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(196): Show | 244 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.2155+488C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319280 | ||||||
| chr12:66319280
|
C | T | 1 | a0002c0001t0001g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2155+488C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319280 | ||||||
| chr12:66319605
|
G | A | 1 | a0009c0014t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2155+813G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319605 | ||||||
| chr12:66319880
|
G | GT | 125 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(122): Show | 158 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.2155+1088_2155+108 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319880 | ||||||
| chr12:66319880
|
G | GTT | 28 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(25): Show | 31 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.2155+1088_2155+108 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319880 | ||||||
| chr12:66319881
|
G | T | 195 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(192): Show | 240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2155+1089G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66319881 | ||||||
| chr12:66320080
|
C | T | 6 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2155+1288C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320080 | ||||||
| chr12:66320113
|
A | G | 1 | a0001c0002t0001g0275 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2155+1321A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320113 | ||||||
| chr12:66320122
|
C | G | 2 | a0012c0016t0001g0139a0012c0016t0001g0140 | 2 | NA18999.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2155+1330C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320122 | ||||||
| chr12:66320198
|
T | C | 32 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(29): Show | 41 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.2155+1406T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320198 | ||||||
| chr12:66320430
|
A | C | 115 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(112): Show | 147 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2156-1518A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320430 | ||||||
| chr12:66320513
|
A | G | 6 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-1435A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320513 | ||||||
| chr12:66320728
|
G | GA | 195 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(192): Show | 240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2156-1220_2156-121 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320728 | ||||||
| chr12:66320812
|
G | A | 2 | a0003c0003t0001g0124a0003c0003t0001g0125 | 2 | NA19060.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2156-1136G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320812 | ||||||
| chr12:66320854
|
G | GA | 6 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-1089dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 66320854 | |||||
| chr12:66320916
|
A | G | 29 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(26): Show | 32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2156-1032A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320916 | ||||||
| chr12:66320975
|
G | A | 29 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(26): Show | 32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2156-973G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320975 | ||||||
| chr12:66320997
|
T | C | 195 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(192): Show | 240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2156-951T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66320997 | ||||||
| chr12:66321000
|
C | T | 7 | a0001c0030t0001g0244a0005c0033t0001g0236a0010c0013t0001g0234others(4): Show | 7 | HG02055.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-948C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321000 | ||||||
| chr12:66321001
|
G | A | 1 | a0002c0001t0001g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2156-947G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321001 | ||||||
| chr12:66321050
|
C | T | 1 | a0002c0001t0001g0103 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2156-898C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321050 | ||||||
| chr12:66321102
|
T | A | 2 | a0001c0029t0001g0178a0005c0015t0001g0177 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2156-846T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321102 | ||||||
| chr12:66321103
|
G | T | 2 | a0001c0029t0001g0178a0005c0015t0001g0177 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2156-845G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321103 | ||||||
| chr12:66321174
|
A | G | 3 | a0001c0002t0001g0231a0001c0002t0001g0232a0001c0002t0001g0233 | 3 | HG02965.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2156-774A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321174 | ||||||
| chr12:66321240
|
C | T | 1 | a0002c0001t0001g0170 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2156-708C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321240 | ||||||
| chr12:66321419
|
T | C | 6 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2156-529T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321419 | ||||||
| chr12:66321539
|
A | G | 1 | a0002c0001t0001g0156 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2156-409A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321539 | ||||||
| chr12:66321631
|
T | C | 3 | a0004c0008t0001g0091a0004c0008t0001g0092a0004c0008t0001g0151 | 3 | HG02280.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2156-317T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321631 | ||||||
| chr12:66321633
|
G | A | 2 | a0002c0001t0001g0029a0002c0001t0001g0121 | 3 | HG02257.hp2 HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2156-315G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321633 | ||||||
| chr12:66321708
|
T | A | 150 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(147): Show | 186 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2156-240T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321708 | ||||||
| chr12:66321793
|
G | A | 1 | a0001c0002t0001g0263 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2156-155G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 7/12 | chr12 | 66321793 | ||||||
| chr12:66322038
|
T | C | 4 | a0006c0007t0001g0293a0011c0020t0001g0228a0011c0020t0001g0230others(1): Show | 4 | HG02145.hp1 HG02145.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2237+9T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322038 | ||||||
| chr12:66322089
|
A | G | 29 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(26): Show | 32 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.2237+60A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322089 | ||||||
| chr12:66322222
|
T | A | 3 | a0001c0018t0001g0043a0001c0018t0001g0259a0001c0018t0001g0281 | 4 | HG02109.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2237+193T>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322222 | ||||||
| chr12:66322271
|
A | G | 115 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(112): Show | 147 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2237+242A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322271 | ||||||
| chr12:66322285
|
G | T | 5 | a0002c0017t0001g0138a0012c0016t0001g0136a0012c0016t0001g0137others(2): Show | 5 | NA18954.hp2 NA18999.hp2 NA19085.hp1 others(2): Show |
intron_variant | MODIFIER | c.2237+256G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | chr12 | 66322285 | ||||||
| chr12:66322565
|
CA | C | 85 | a0001c0046t0001g0288a0002c0001t0001g0015a0002c0001t0001g0027others(82): Show | 115 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.2238-142delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 66322565 | |||||
| chr12:66322565
|
CAAA | C | 93 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(90): Show | 125 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.2238-144_2238-142d others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 66322565 | |||||
| chr12:66322565
|
CAAAA | C | 101 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(98): Show | 114 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(111): Show |
intron_variant | MODIFIER | c.2238-145_2238-142d others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 66322565 | |||||
| chr12:66323039
|
A | G | 6 | a0006c0007t0001g0041a0006c0007t0001g0225a0006c0010t0001g0040others(3): Show | 7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2297+256A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323039 | ||||||
| chr12:66323064
|
G | A | 150 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(147): Show | 186 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2297+281G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323064 | ||||||
| chr12:66323246
|
A | T | 1 | a0002c0001t0001g0053 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2297+463A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323246 | ||||||
| chr12:66323333
|
C | G | 1 | a0004c0004t0001g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2297+550C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323333 | ||||||
| chr12:66323422
|
C | T | 45 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(42): Show | 54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2298-561C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323422 | ||||||
| chr12:66323423
|
G | A | 7 | a0006c0007t0001g0041a0006c0007t0001g0225a0006c0007t0001g0226others(4): Show | 8 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2298-560G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323423 | ||||||
| chr12:66323680
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2298-303G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323680 | ||||||
| chr12:66323912
|
T | G | 195 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(192): Show | 240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2298-71T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323912 | ||||||
| chr12:66323916
|
T | C | 1 | a0003c0003t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2298-67T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323916 | ||||||
| chr12:66323936
|
C | T | 195 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(192): Show | 240 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(237): Show |
intron_variant | MODIFIER | c.2298-47C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 9/12 | chr12 | 66323936 | ||||||
| chr12:66324218
|
GA | G | 45 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(42): Show | 54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2526+11delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 66324218 | |||||
| chr12:66324230
|
T | G | 1 | a0009c0014t0001g0064 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2526+19T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324230 | ||||||
| chr12:66324427
|
G | T | 45 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(42): Show | 54 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.2526+216G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324427 | ||||||
| chr12:66324499
|
G | A | 1 | a0006c0007t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2526+288G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324499 | ||||||
| chr12:66324590
|
T | C | 1 | a0001c0030t0001g0244 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2526+379T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324590 | ||||||
| chr12:66324885
|
A | G | 2 | a0001c0002t0001g0276a0001c0002t0001g0277 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2527-98A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324885 | ||||||
| chr12:66324953
|
A | G | 1 | a0006c0007t0001g0213 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2527-30A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 10/12 | chr12 | 66324953 | ||||||
| chr12:66325177
|
C | T | 4 | a0001c0022t0001g0174a0004c0008t0001g0160a0004c0008t0001g0161others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+51C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325177 | ||||||
| chr12:66325193
|
C | G | 36 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(33): Show | 45 | HG00438.hp2 HG00621.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.2670+67C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325193 | ||||||
| chr12:66325272
|
C | T | 105 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(102): Show | 136 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2670+146C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325272 | ||||||
| chr12:66325297
|
C | G | 1 | a0002c0001t0001g0155 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2670+171C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325297 | ||||||
| chr12:66325370
|
C | T | 1 | a0002c0001t0001g0165 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2670+244C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325370 | ||||||
| chr12:66325445
|
A | G | 1 | a0002c0001t0002g0198 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2670+319A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325445 | ||||||
| chr12:66325496
|
G | A | 1 | a0002c0037t0001g0158 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2670+370G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325496 | ||||||
| chr12:66325545
|
G | C | 7 | a0006c0007t0001g0041a0006c0007t0001g0225a0006c0007t0001g0226others(4): Show | 8 | HG01884.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2670+419G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325545 | ||||||
| chr12:66325572
|
T | C | 1 | a0001c0024t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2670+446T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325572 | ||||||
| chr12:66325598
|
G | A | 1 | a0005c0015t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2670+472G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325598 | ||||||
| chr12:66325873
|
C | A | 1 | a0001c0046t0001g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2670+747C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66325873 | ||||||
| chr12:66326015
|
T | C | 78 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(75): Show | 105 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2670+889T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326015 | ||||||
| chr12:66326195
|
A | C | 1 | a0001c0002t0001g0271 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2670+1069A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326195 | ||||||
| chr12:66326537
|
G | A | 4 | a0012c0016t0001g0136a0012c0016t0001g0137a0012c0016t0001g0139others(1): Show | 4 | NA18999.hp2 NA19085.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1411G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326537 | ||||||
| chr12:66326724
|
AT | A | 167 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(164): Show | 214 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.2670+1610delT | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66326724 | |||||
| chr12:66326797
|
C | T | 2 | a0002c0001t0001g0053a0009c0014t0001g0064 | 2 | HG02109.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2670+1671C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66326797 | ||||||
| chr12:66327028
|
T | C | 4 | a0005c0015t0001g0050a0005c0015t0001g0177a0005c0015t0001g0179others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1902T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327028 | ||||||
| chr12:66327035
|
C | CA | 5 | a0001c0002t0001g0044a0004c0004t0001g0080a0004c0004t0001g0127others(2): Show | 6 | HG00621.hp1 HG00642.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.2670+1941dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327035 | |||||
| chr12:66327035
|
CA | C | 119 | a0001c0002t0001g0008a0001c0002t0001g0045a0001c0002t0001g0049others(116): Show | 167 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.2670+1941delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327035 | |||||
| chr12:66327035
|
CAA | C | 23 | a0001c0002t0001g0270a0001c0005t0001g0061a0001c0005t0001g0173others(20): Show | 24 | HG00140.hp1 HG00558.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327035 | |||||
| chr12:66327054
|
A | ATATATAT others(16): Show |
1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2670+1928_2670+192 others(27): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327054 | ||||||
| chr12:66327054
|
A | T | 1 | a0006c0007t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2670+1928A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327054 | ||||||
| chr12:66327056
|
A | T | 2 | a0004c0035t0001g0183a0006c0007t0001g0226 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2670+1930A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327056 | ||||||
| chr12:66327058
|
A | T | 16 | a0002c0001t0001g0027a0002c0001t0001g0053a0002c0001t0001g0099others(13): Show | 17 | HG01168.hp2 HG01258.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2670+1932A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327058 | ||||||
| chr12:66327060
|
A | AATATATA others(5): Show |
2 | a0006c0007t0001g0213a0006c0007t0001g0229 | 2 | HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2670+1935_2670+193 others(16): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327060 | |||||
| chr12:66327060
|
A | AATATATA others(7): Show |
1 | a0005c0033t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2670+1935_2670+193 others(18): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327060 | |||||
| chr12:66327060
|
A | AT | 3 | a0003c0003t0001g0082a0009c0014t0001g0062a0009c0014t0001g0066 | 3 | HG01167.hp1 HG01243.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2670+1934_2670+193 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327060 | ||||||
| chr12:66327060
|
A | T | 50 | a0001c0002t0001g0232a0001c0005t0001g0020a0001c0005t0001g0021others(47): Show | 60 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.2670+1934A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327060 | ||||||
| chr12:66327062
|
A | AATATATA others(3): Show |
1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2670+1937_2670+193 others(14): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327062 | |||||
| chr12:66327062
|
A | AT | 3 | a0001c0002t0001g0231a0001c0002t0001g0289a0006c0010t0001g0250 | 3 | HG01261.hp2 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2670+1936_2670+193 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327062 | ||||||
| chr12:66327062
|
A | T | 167 | a0001c0002t0001g0232a0001c0005t0001g0003a0001c0005t0001g0018others(164): Show | 211 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.2670+1936A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327062 | ||||||
| chr12:66327064
|
A | AATATATA others(17): Show |
1 | a0011c0027t0001g0223 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2670+1939_2670+194 others(28): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | |||||
| chr12:66327064
|
A | AATATATA others(21): Show |
2 | a0002c0001t0002g0186a0002c0001t0002g0200 | 2 | HG03704.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2670+1939_2670+194 others(32): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | |||||
| chr12:66327064
|
A | AATATATA others(23): Show |
3 | a0002c0001t0002g0038a0002c0001t0002g0208a0005c0006t0002g0268 | 4 | HG01496.hp2 NA18971.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1939_2670+194 others(34): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | |||||
| chr12:66327064
|
A | AATATATA others(27): Show |
1 | a0005c0006t0002g0262 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2670+1939_2670+194 others(38): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | |||||
| chr12:66327064
|
A | AATATATA others(45): Show |
1 | a0022c0041t0002g0188 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2670+1939_2670+194 others(56): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327064 | |||||
| chr12:66327064
|
A | AT | 4 | a0001c0002t0001g0233a0001c0002t0001g0269a0001c0002t0001g0295others(1): Show | 4 | HG01346.hp1 NA18906.hp1 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.2670+1938_2670+193 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | ||||||
| chr12:66327064
|
A | ATATATAT others(22): Show |
1 | a0002c0001t0002g0211 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2670+1938_2670+193 others(33): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | ||||||
| chr12:66327064
|
A | ATATATAT others(28): Show |
1 | a0002c0001t0002g0210 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2670+1938_2670+193 others(39): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | ||||||
| chr12:66327064
|
A | T | 188 | a0001c0002t0001g0014a0001c0002t0001g0231a0001c0002t0001g0232others(185): Show | 239 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.2670+1938A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327064 | ||||||
| chr12:66327066
|
A | AAAAAAAA others(19): Show |
1 | a0005c0015t0001g0299 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(30): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AAAAAATA others(31): Show |
1 | a0002c0001t0002g0192 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(42): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AAAAATAT others(26): Show |
1 | a0021c0040t0002g0193 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(37): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AAAATATA others(21): Show |
1 | a0005c0015t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(32): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AAAATATA others(25): Show |
2 | a0002c0001t0002g0198a0002c0001t0002g0201 | 2 | NA19004.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2670+1941_2670+194 others(36): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AAAATATA others(27): Show |
1 | a0002c0001t0002g0184 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(38): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AAAATATA others(29): Show |
1 | a0005c0006t0002g0240 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(40): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AAATATAT others(30): Show |
1 | a0002c0001t0002g0194 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2670+1941_2670+194 others(41): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AATATATA others(11): Show |
1 | a0005c0015t0001g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2670+1956_2670+195 others(22): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AATATATA others(19): Show |
2 | a0002c0001t0002g0206a0016c0021t0001g0221 | 2 | HG01952.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2670+1956_2670+195 others(30): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AATATATA others(23): Show |
3 | a0002c0001t0002g0202a0002c0001t0002g0204a0002c0001t0002g0205 | 3 | NA18942.hp1 NA18953.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2670+1956_2670+195 others(34): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AATATATA others(25): Show |
1 | a0002c0001t0002g0052 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2670+1956_2670+195 others(36): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AATATATA others(29): Show |
1 | a0026c0042t0002g0195 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2670+1956_2670+195 others(40): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327066 | |||||
| chr12:66327066
|
A | AT | 3 | a0001c0002t0001g0013a0001c0050t0001g0013a0004c0004t0001g0105 | 4 | HG03942.hp2 HG04204.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | ATATATAT others(10): Show |
1 | a0005c0015t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2670+1940_2670+194 others(21): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | ATATATAT others(18): Show |
1 | a0011c0027t0001g0220 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2670+1940_2670+194 others(29): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | ATATATAT others(20): Show |
2 | a0002c0001t0002g0037a0002c0001t0002g0185 | 3 | HG01361.hp2 HG02273.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(31): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | ATATATAT others(22): Show |
3 | a0002c0001t0002g0039a0002c0001t0002g0207a0016c0021t0001g0222 | 4 | HG01255.hp2 HG01358.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(33): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | ATATATAT others(24): Show |
2 | a0004c0004t0001g0190a0016c0021t0001g0224 | 2 | HG02809.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(35): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | ATATATAT others(26): Show |
1 | a0002c0001t0002g0199 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2670+1940_2670+194 others(37): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | ATATATAT others(28): Show |
5 | a0002c0001t0002g0101a0002c0001t0002g0191a0002c0001t0002g0196others(2): Show | 5 | HG02071.hp1 NA18950.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.2670+1940_2670+194 others(39): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327066
|
A | T | 234 | a0001c0002t0001g0005a0001c0002t0001g0014a0001c0002t0001g0045others(231): Show | 292 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(289): Show |
intron_variant | MODIFIER | c.2670+1940A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327066 | ||||||
| chr12:66327321
|
C | G | 167 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(164): Show | 214 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.2670+2195C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327321 | ||||||
| chr12:66327342
|
T | C | 1 | a0006c0007t0001g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2670+2216T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327342 | ||||||
| chr12:66327566
|
G | GT | 25 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0032others(22): Show | 34 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2670+2440_2670+244 others(5): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327566 | ||||||
| chr12:66327567
|
G | C | 25 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0032others(22): Show | 34 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.2670+2441G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327567 | ||||||
| chr12:66327567
|
G | GTTC | 142 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(139): Show | 180 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.2670+2443_2670+244 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327567 | |||||
| chr12:66327761
|
A | G | 167 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(164): Show | 214 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.2670+2635A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327761 | ||||||
| chr12:66327793
|
T | TA | 34 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(31): Show | 37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.2670+2675dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66327793 | |||||
| chr12:66327949
|
G | A | 2 | a0004c0008t0001g0160a0004c0008t0001g0161 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2670+2823G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66327949 | ||||||
| chr12:66328011
|
G | A | 1 | a0006c0007t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2670+2885G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328011 | ||||||
| chr12:66328011
|
G | C | 2 | a0002c0001t0002g0196a0021c0040t0002g0193 | 2 | NA18950.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.2670+2885G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328011 | ||||||
| chr12:66328056
|
A | G | 4 | a0001c0002t0001g0012a0001c0002t0001g0253a0001c0002t0001g0282others(1): Show | 5 | NA18984.hp1 NA19011.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670+2930A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328056 | ||||||
| chr12:66328079
|
G | A | 1 | a0006c0010t0001g0227 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2670+2953G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328079 | ||||||
| chr12:66328172
|
G | C | 1 | a0006c0007t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2671-2982G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328172 | ||||||
| chr12:66328337
|
A | G | 164 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(161): Show | 211 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.2671-2817A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328337 | ||||||
| chr12:66328455
|
C | T | 1 | a0004c0004t0001g0176 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2671-2699C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328455 | ||||||
| chr12:66328498
|
G | T | 2 | a0011c0027t0001g0220a0011c0027t0001g0223 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2671-2656G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328498 | ||||||
| chr12:66328578
|
C | G | 1 | a0004c0008t0001g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2671-2576C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328578 | ||||||
| chr12:66328665
|
A | C | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2671-2489A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328665 | ||||||
| chr12:66328803
|
AATG | A | 33 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(30): Show | 36 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.2671-2345_2671-234 others(7): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 66328803 | |||||
| chr12:66328811
|
T | G | 1 | a0005c0006t0001g0273 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2671-2343T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328811 | ||||||
| chr12:66328886
|
G | T | 1 | a0004c0008t0001g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2671-2268G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66328886 | ||||||
| chr12:66329160
|
A | G | 2 | a0002c0001t0001g0099a0002c0001t0001g0165 | 2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2671-1994A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329160 | ||||||
| chr12:66329336
|
G | A | 1 | a0014c0025t0001g0291 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2671-1818G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329336 | ||||||
| chr12:66329513
|
A | G | 3 | a0002c0001t0001g0029a0002c0001t0001g0054a0002c0001t0001g0121 | 4 | HG01074.hp2 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2671-1641A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329513 | ||||||
| chr12:66329538
|
G | A | 2 | a0011c0027t0001g0220a0011c0027t0001g0223 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2671-1616G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329538 | ||||||
| chr12:66329736
|
G | A | 34 | a0001c0005t0001g0003a0001c0005t0001g0018a0001c0005t0001g0019others(31): Show | 43 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.2671-1418G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329736 | ||||||
| chr12:66329768
|
A | G | 1 | a0002c0001t0002g0210 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2671-1386A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66329768 | ||||||
| chr12:66330166
|
A | G | 1 | a0003c0003t0001g0146 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2671-988A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66330166 | ||||||
| chr12:66330691
|
G | A | 4 | a0005c0015t0001g0050a0005c0015t0001g0177a0005c0015t0001g0179others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2671-463G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66330691 | ||||||
| chr12:66330760
|
C | A | 1 | a0002c0001t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2671-394C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 11/12 | chr12 | 66330760 | ||||||
| chr12:66331790
|
C | A | 1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3162+145C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66331790 | ||||||
| chr12:66332116
|
A | G | 1 | a0003c0003t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3162+471A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332116 | ||||||
| chr12:66332132
|
C | A | 159 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(156): Show | 201 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.3162+487C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332132 | ||||||
| chr12:66332421
|
G | C | 1 | a0003c0003t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3162+776G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332421 | ||||||
| chr12:66332575
|
G | A | 115 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(112): Show | 154 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.3162+930G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332575 | ||||||
| chr12:66332659
|
C | T | 180 | a0001c0022t0001g0174a0001c0024t0001g0180a0001c0024t0001g0181others(177): Show | 223 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(220): Show |
intron_variant | MODIFIER | c.3162+1014C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66332659 | ||||||
| chr12:66333239
|
T | C | 1 | a0001c0018t0001g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3162+1594T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333239 | ||||||
| chr12:66333571
|
C | T | 1 | a0003c0003t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3162+1926C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333571 | ||||||
| chr12:66333599
|
G | C | 1 | a0005c0015t0001g0179 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3162+1954G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333599 | ||||||
| chr12:66333615
|
T | C | 4 | a0005c0015t0001g0050a0005c0015t0001g0177a0005c0015t0001g0179others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3162+1970T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333615 | ||||||
| chr12:66333628
|
A | G | 159 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(156): Show | 201 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.3162+1983A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333628 | ||||||
| chr12:66333788
|
A | G | 159 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(156): Show | 201 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.3162+2143A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333788 | ||||||
| chr12:66333823
|
T | C | 1 | a0002c0001t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3162+2178T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333823 | ||||||
| chr12:66333862
|
T | C | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3162+2217T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333862 | ||||||
| chr12:66333864
|
C | T | 1 | a0003c0003t0001g0011 | 3 | HG01123.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3162+2219C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333864 | ||||||
| chr12:66333965
|
G | T | 4 | a0005c0015t0001g0050a0005c0015t0001g0177a0005c0015t0001g0179others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3162+2320G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66333965 | ||||||
| chr12:66334029
|
A | G | 1 | a0006c0007t0001g0225 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3162+2384A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334029 | ||||||
| chr12:66334051
|
G | T | 309 | a0001c0002t0001g0002a0001c0002t0001g0005a0001c0002t0001g0008others(306): Show | 388 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.3162+2406G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334051 | ||||||
| chr12:66334052
|
C | T | 1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3162+2407C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334052 | ||||||
| chr12:66334053
|
G | T | 155 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(152): Show | 197 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(194): Show |
intron_variant | MODIFIER | c.3162+2408G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334053 | ||||||
| chr12:66334092
|
C | T | 1 | a0003c0003t0001g0112 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3162+2447C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334092 | ||||||
| chr12:66334170
|
C | A | 6 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3162+2525C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334170 | ||||||
| chr12:66334275
|
A | G | 1 | a0014c0048t0001g0255 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3162+2630A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334275 | ||||||
| chr12:66334422
|
G | A | 34 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(31): Show | 37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.3162+2777G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334422 | ||||||
| chr12:66334454
|
C | G | 159 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(156): Show | 201 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.3162+2809C>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334454 | ||||||
| chr12:66334471
|
GA | G | 125 | a0001c0022t0001g0174a0001c0024t0001g0180a0001c0024t0001g0181others(122): Show | 161 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.3162+2843delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334471 | |||||
| chr12:66334471
|
GAA | G | 35 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(32): Show | 38 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.3162+2842_3162+284 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334471 | |||||
| chr12:66334501
|
A | C | 1 | a0005c0044t0001g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3162+2856A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334501 | ||||||
| chr12:66334524
|
T | C | 1 | a0005c0015t0001g0177 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3162+2879T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334524 | ||||||
| chr12:66334549
|
C | T | 12 | a0005c0023t0001g0067a0005c0023t0001g0068a0005c0023t0001g0069others(9): Show | 13 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3162+2904C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334549 | ||||||
| chr12:66334550
|
G | A | 1 | a0004c0004t0001g0190 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3162+2905G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334550 | ||||||
| chr12:66334752
|
C | A | 2 | a0001c0002t0001g0263a0001c0002t0001g0298 | 2 | HG00738.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.3162+3107C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334752 | ||||||
| chr12:66334780
|
A | AAAAT | 19 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(16): Show | 20 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.3162+3153_3162+315 others(8): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334780 | |||||
| chr12:66334780
|
AAAAT | A | 114 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(111): Show | 153 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.3162+3153_3162+315 others(8): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66334780 | |||||
| chr12:66334798
|
A | C | 120 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(117): Show | 159 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(156): Show |
intron_variant | MODIFIER | c.3162+3153A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334798 | ||||||
| chr12:66334920
|
G | T | 1 | a0002c0001t0001g0117 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3163-3081G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334920 | ||||||
| chr12:66334962
|
G | C | 3 | a0011c0020t0001g0228a0011c0020t0001g0230a0011c0020t0001g0292 | 3 | HG02145.hp2 HG02895.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3163-3039G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334962 | ||||||
| chr12:66334990
|
G | C | 1 | a0001c0002t0001g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3163-3011G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66334990 | ||||||
| chr12:66335010
|
A | T | 2 | a0001c0005t0001g0058a0001c0005t0001g0059 | 2 | HG00438.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.3163-2991A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335010 | ||||||
| chr12:66335062
|
G | A | 159 | a0002c0001t0001g0006a0002c0001t0001g0007a0002c0001t0001g0015others(156): Show | 201 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.3163-2939G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335062 | ||||||
| chr12:66335140
|
T | C | 34 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(31): Show | 37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.3163-2861T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335140 | ||||||
| chr12:66335420
|
G | C | 1 | a0005c0044t0001g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3163-2581G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335420 | ||||||
| chr12:66335457
|
A | G | 3 | a0001c0018t0001g0043a0001c0018t0001g0259a0001c0018t0001g0281 | 4 | HG02109.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3163-2544A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335457 | ||||||
| chr12:66335470
|
T | C | 180 | a0001c0022t0001g0174a0001c0024t0001g0180a0001c0024t0001g0181others(177): Show | 223 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(220): Show |
intron_variant | MODIFIER | c.3163-2531T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335470 | ||||||
| chr12:66335535
|
G | T | 1 | a0001c0022t0001g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3163-2466G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335535 | ||||||
| chr12:66335536
|
G | C | 1 | a0003c0003t0001g0030 | 2 | HG00558.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.3163-2465G>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335536 | ||||||
| chr12:66335603
|
A | C | 34 | a0002c0001t0002g0037a0002c0001t0002g0038a0002c0001t0002g0039others(31): Show | 37 | HG01255.hp2 HG01358.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.3163-2398A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66335603 | ||||||
| chr12:66336088
|
T | G | 1 | a0004c0004t0001g0190 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3163-1913T>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336088 | ||||||
| chr12:66336211
|
T | C | 13 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3163-1790T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336211 | ||||||
| chr12:66336617
|
G | T | 4 | a0002c0001t0001g0098a0002c0017t0001g0016a0002c0017t0001g0055others(1): Show | 5 | NA18939.hp2 NA18952.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163-1384G>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336617 | ||||||
| chr12:66336760
|
T | C | 14 | a0001c0022t0001g0174a0001c0024t0001g0180a0001c0024t0001g0181others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3163-1241T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336760 | ||||||
| chr12:66336813
|
G | A | 1 | a0004c0035t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3163-1188G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336813 | ||||||
| chr12:66336833
|
C | T | 13 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3163-1168C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336833 | ||||||
| chr12:66336840
|
C | T | 1 | a0001c0002t0001g0276 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3163-1161C>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336840 | ||||||
| chr12:66336862
|
CTG | C | 5 | a0011c0027t0001g0220a0011c0027t0001g0223a0016c0021t0001g0221others(2): Show | 5 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163-1136_3163-113 others(6): Show |
HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66336862 | |||||
| chr12:66336889
|
A | G | 14 | a0001c0022t0001g0174a0001c0024t0001g0180a0001c0024t0001g0181others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3163-1112A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66336889 | ||||||
| chr12:66337039
|
G | A | 1 | a0003c0003t0001g0212 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3163-962G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337039 | ||||||
| chr12:66337301
|
A | T | 4 | a0007c0009t0001g0042a0007c0009t0001g0243a0007c0009t0001g0245others(1): Show | 5 | HG01884.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3163-700A>T | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337301 | ||||||
| chr12:66337418
|
C | A | 6 | a0005c0033t0001g0236a0011c0027t0001g0220a0011c0027t0001g0223others(3): Show | 6 | HG02809.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3163-583C>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337418 | ||||||
| chr12:66337505
|
T | C | 1 | a0005c0033t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3163-496T>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337505 | ||||||
| chr12:66337563
|
G | A | 1 | a0001c0002t0001g0275 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3163-438G>A | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337563 | ||||||
| chr12:66337619
|
T | TA | 6 | a0001c0002t0001g0269a0003c0003t0001g0124a0004c0004t0001g0097others(3): Show | 6 | HG01192.hp1 NA18952.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.3163-366dupA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66337619 | |||||
| chr12:66337619
|
TA | T | 25 | a0001c0024t0001g0180a0001c0024t0001g0181a0001c0024t0001g0182others(22): Show | 25 | HG01074.hp2 HG01168.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.3163-366delA | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 66337619 | |||||
| chr12:66337635
|
A | C | 1 | a0014c0025t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3163-366A>C | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337635 | ||||||
| chr12:66337643
|
A | G | 1 | a0003c0003t0001g0011 | 3 | HG01123.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.3163-358A>G | HELB | ENSG00000127311.10 | transcript | ENST00000247815.9 | protein_coding | 12/12 | chr12 | 66337643 |