Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1975 |
|---|---|
| ensemblid | ENSG00000063046.18 |
| hgncid | 3285 |
| symbol | EIF4B |
| name | eukaryotic translation initiation factor 4B |
| refseq_nuc | NM_001417.7 |
| refseq_prot | NP_001408.2 |
| ensembl_nuc | ENST00000262056.14 |
| ensembl_prot | ENSP00000262056.9 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 53006456 |
| end | 53042215 |
| strand | + |
| ver | v1.2 |
| region | chr12:53006456-53042215 |
| region5000 | chr12:53001456-53047215 |
| regionname0 | EIF4B_chr12_53006456_53042215 |
| regionname5000 | EIF4B_chr12_53001456_53047215 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 611 | 365 | 95 | 65 | 153 | 10 | 40 | 119 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0002 | 0/0 | 611 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0003 | 0/0 | 611 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0004 | 0/0 | 601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1836 | 258 | 40 | 60 | 110 | 10 | 37 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0002 | 0/0 | 1836 | 91 | 43 | 5 | 41 | 0 | 2 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0003 | 1/0 | 1836 | 8 | 7 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0004 | 0/0 | 1836 | 5 | 0 | 5 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0005 | 0/0 | 1836 | 5 | 5 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0006 | 0/0 | 1836 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0007 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0008 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| c0009 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2024 | 141 | 4 | 45 | 59 | 7 | 25 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0002 | 0/0 | 2025 | 100 | 28 | 16 | 47 | 1 | 8 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0003 | 0/0 | 2024 | 34 | 1 | 1 | 32 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0004 | 0/0 | 2024 | 27 | 18 | 3 | 4 | 0 | 2 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0005 | 1/0 | 2021 | 19 | 17 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0006 | 0/0 | 2027 | 7 | 2 | 1 | 0 | 1 | 3 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0007 | 0/0 | 2021 | 6 | 6 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0008 | 0/0 | 2025 | 5 | 0 | 0 | 4 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0009 | 0/0 | 2021 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0010 | 0/0 | 2021 | 3 | 0 | 1 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0011 | 0/0 | 2024 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0012 | 0/0 | 2024 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0013 | 0/0 | 2021 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0014 | 0/0 | 2024 | 2 | 0 | 1 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0015 | 0/0 | 2024 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0016 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0017 | 0/0 | 2024 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0018 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0019 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0020 | 0/0 | 2021 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0021 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0022 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0023 | 0/0 | 2024 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0024 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0025 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0026 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0027 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0028 | 0/0 | 2025 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| t0029 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1836 | 258 | 40 | 60 | 110 | 10 | 37 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002 | 0/0 | 1836 | 91 | 43 | 5 | 41 | 0 | 2 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0003 | 1/0 | 1836 | 8 | 7 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0005 | 0/0 | 1836 | 5 | 5 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0006 | 0/0 | 1836 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0007 | 0/0 | 1836 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0002c0004 | 0/0 | 1836 | 5 | 0 | 5 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0003c0009 | 0/0 | 1836 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0004c0008 | 0/0 | 1806 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3859 | 133 | 4 | 41 | 56 | 7 | 24 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0002 | 0/0 | 3860 | 100 | 28 | 16 | 47 | 1 | 8 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0006 | 0/0 | 3862 | 7 | 2 | 1 | 0 | 1 | 3 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0008 | 0/0 | 3860 | 5 | 0 | 0 | 4 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0010 | 0/0 | 3856 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0014 | 0/0 | 3859 | 2 | 0 | 1 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0016 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0017 | 0/0 | 3859 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0021 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0022 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0023 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0024 | 0/0 | 3860 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0027 | 0/0 | 3860 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0028 | 0/0 | 3860 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0001t0029 | 0/0 | 3860 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0003 | 0/0 | 3859 | 34 | 1 | 1 | 32 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0004 | 0/0 | 3859 | 27 | 18 | 3 | 4 | 0 | 2 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0005 | 0/0 | 3856 | 9 | 8 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0007 | 0/0 | 3856 | 6 | 6 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0009 | 0/0 | 3856 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0011 | 0/0 | 3859 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0012 | 0/0 | 3859 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0015 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0018 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0019 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0020 | 0/0 | 3856 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0025 | 0/0 | 3860 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0002t0026 | 0/0 | 3860 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0003t0005 | 1/0 | 3856 | 8 | 7 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0005t0005 | 0/0 | 3856 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0005t0013 | 0/0 | 3856 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0006t0001 | 0/0 | 3859 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0001c0007t0001 | 0/0 | 3859 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0002c0004t0001 | 0/0 | 3859 | 4 | 0 | 4 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0002c0004t0010 | 0/0 | 3856 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0003c0009t0015 | 0/0 | 3859 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| a0004c0008t0001 | 0/0 | 3829 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | copy fasta | chr12 | 53001456 | 53047215 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0109 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0010g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0014g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0014g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0016g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0017g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0021g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0023g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0024g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0027g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0028g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0001t0029g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0009g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0009g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0011g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0011g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0011g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0012g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0012g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0012g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0015g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0018g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0019g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0020g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0025g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0002t0026g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0317 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0003t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0013g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0005t0013g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0006t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0006t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0001c0007t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0002c0004t0010g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0003c0009t0015g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| a0004c0008t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00423 | hp1 | a0001 | c0002 | t0012 | g0290 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0310 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00438 | hp1 | a0001 | c0006 | t0001 | g0153 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00544 | hp1 | a0001 | c0001 | t0029 | g0196 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0347 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01070 | hp1 | a0002 | c0004 | t0010 | g0050 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0315 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0297 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01169 | hp1 | a0001 | c0002 | t0004 | g0296 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01192 | hp2 | a0002 | c0004 | t0001 | g0052 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01255 | hp2 | a0001 | c0002 | t0004 | g0274 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01256 | hp1 | a0001 | c0001 | t0014 | g0014 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01257 | hp1 | a0002 | c0004 | t0001 | g0103 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01258 | hp2 | a0002 | c0004 | t0001 | g0105 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01884 | hp1 | a0001 | c0002 | t0009 | g0319 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01891 | hp1 | a0001 | c0002 | t0011 | g0359 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02040 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02055 | hp2 | a0001 | c0002 | t0005 | g0332 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0308 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0314 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0316 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02145 | hp1 | a0001 | c0002 | t0009 | g0318 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0329 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02148 | hp1 | a0001 | c0001 | t0017 | g0079 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0284 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0327 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0117 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02451 | hp1 | a0001 | c0002 | t0018 | g0292 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0159 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0313 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02572 | hp1 | a0001 | c0002 | t0011 | g0361 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0275 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02615 | hp2 | a0001 | c0003 | t0005 | g0323 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02622 | hp1 | a0001 | c0003 | t0005 | g0321 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02630 | hp1 | a0001 | c0001 | t0027 | g0184 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0277 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0280 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0183 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0326 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0335 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0286 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02886 | hp2 | a0001 | c0002 | t0004 | g0276 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0303 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02895 | hp2 | a0001 | c0001 | t0021 | g0025 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02896 | hp1 | a0001 | c0002 | t0007 | g0339 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0301 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0294 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0299 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0279 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0295 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02970 | hp2 | a0001 | c0005 | t0005 | g0009 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0300 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02976 | hp2 | a0001 | c0002 | t0007 | g0270 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0037 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03041 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03098 | hp2 | a0001 | c0002 | t0004 | g0302 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03130 | hp1 | a0001 | c0001 | t0024 | g0228 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03195 | hp1 | a0001 | c0002 | t0019 | g0278 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03209 | hp2 | a0001 | c0002 | t0020 | g0342 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03225 | hp1 | a0001 | c0002 | t0009 | g0341 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0330 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03453 | hp1 | a0001 | c0002 | t0007 | g0338 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0328 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03486 | hp1 | a0001 | c0002 | t0004 | g0005 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03486 | hp2 | a0001 | c0002 | t0011 | g0360 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03516 | hp1 | a0003 | c0009 | t0015 | g0304 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ESN | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03540 | hp1 | a0001 | c0003 | t0005 | g0325 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0340 | AFR | GWD | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0322 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0246 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03688 | hp2 | a0001 | c0007 | t0001 | g0101 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0245 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0287 | SAS | PJL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0289 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04204 | hp2 | a0001 | c0001 | t0028 | g0224 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18522 | hp1 | a0001 | c0005 | t0005 | g0009 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18906 | hp1 | a0001 | c0002 | t0007 | g0337 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0204 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0349 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0271 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0283 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0199 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0348 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18952 | hp1 | a0001 | c0006 | t0001 | g0125 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0346 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18954 | hp1 | a0001 | c0002 | t0026 | g0343 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18956 | hp2 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0357 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18969 | hp2 | a0001 | c0001 | t0010 | g0144 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0305 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18978 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0345 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18990 | hp2 | a0001 | c0002 | t0012 | g0285 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0358 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18993 | hp1 | a0001 | c0002 | t0003 | g0350 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0356 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0306 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0320 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19000 | hp1 | a0001 | c0002 | t0004 | g0282 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19000 | hp2 | a0004 | c0008 | t0001 | g0152 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19001 | hp2 | a0001 | c0002 | t0025 | g0355 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0311 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0344 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19030 | hp1 | a0001 | c0001 | t0022 | g0263 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19030 | hp2 | a0001 | c0005 | t0013 | g0272 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19043 | hp1 | a0001 | c0002 | t0004 | g0293 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19043 | hp2 | a0001 | c0002 | t0005 | g0333 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19055 | hp1 | a0001 | c0001 | t0008 | g0031 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0354 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0352 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0351 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0307 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19065 | hp1 | a0001 | c0001 | t0008 | g0181 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0353 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0309 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19091 | hp1 | a0001 | c0002 | t0012 | g0273 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19240 | hp1 | a0001 | c0002 | t0004 | g0005 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA19240 | hp2 | a0001 | c0002 | t0015 | g0281 | AFR | YRI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20129 | hp1 | a0001 | c0005 | t0013 | g0312 | AFR | ASW | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ASW | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20752 | hp1 | a0001 | c0001 | t0014 | g0071 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0032 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0229 | EUR | TSI | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | GIH | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02109 | hp2 | a0001 | c0002 | t0005 | g0324 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0291 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0298 | AFR | ACB | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0362 | AFR | MSL | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG06807 | hp1 | a0001 | c0005 | t0013 | g0334 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0331 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | USA | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0092 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| NA21309 | hp2 | a0001 | c0002 | t0007 | g0336 | AFR | LWK | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0109 | REF | REF | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0005 | g0317 | REF | REF | EIF4B_chr12_53001456_53047215 | EIF4B | chr12 | 53001456 | 53047215 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53037514
|
T | A | 1 | a0002 | 5 | HG01070.hp1 HG01192.hp2 HG01257.hp1 others(2): Show |
missense_variant | MODERATE | c.1412T>A | p.Leu471Gln | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/15 | 1440/3856 | 1412/1836 | 471/611 | chr12 | 53037514 | ||
| chr12:53039625
|
TGCAGGAA others(27): Show |
T | 1 | a0004 | 1 | NA19000.hp2 | splice_acceptor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1683-4_1712delGCAG others(30): Show |
p.Lys562_Arg571del | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/15 | 1683/1836 | 561/611 | chr12 | 53039625 | |||
| chr12:53040177
|
C | T | 1 | a0003 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.1790C>T | p.Ser597Phe | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1818/3856 | 1790/1836 | 597/611 | chr12 | 53040177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53028118
|
C | T | 1 | a0001c0006 | 2 | HG00438.hp1 NA18952.hp1 |
synonymous_variant | LOW | c.909C>T | p.Asp303Asp | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/15 | 937/3856 | 909/1836 | 303/611 | chr12 | 53028118 | ||
| chr12:53033813
|
C | G | 1 | a0001c0005 | 5 | HG02970.hp2 HG06807.hp1 NA18522.hp1 others(2): Show |
synonymous_variant | LOW | c.987C>G | p.Pro329Pro | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 9/15 | 1015/3856 | 987/1836 | 329/611 | chr12 | 53033813 | ||
| chr12:53034032
|
G | A | 1 | a0001c0007 | 1 | HG03688.hp2 | splice_region_variant&synonymous_variant | LOW | c.1206G>A | p.Glu402Glu | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 9/15 | 1234/3856 | 1206/1836 | 402/611 | chr12 | 53034032 | ||
| chr12:53039305
|
C | A | 8 | a0001c0001a0001c0002a0001c0005others(5): Show | 364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
synonymous_variant | LOW | c.1644C>A | p.Gly548Gly | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/15 | 1672/3856 | 1644/1836 | 548/611 | chr12 | 53039305 | ||
| chr12:53039702
|
C | T | 5 | a0001c0001a0001c0006a0001c0007others(2): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
splice_region_variant&synonymous_variant | LOW | c.1755C>T | p.Ser585Ser | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/15 | 1783/3856 | 1755/1836 | 585/611 | chr12 | 53039702 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53006459
|
T | C | 1 | a0001c0002t0009 | 3 | HG01884.hp1 HG02145.hp1 HG03225.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/15 | chr12 | 53006459 | ||||||
| chr12:53040260
|
C | T | 2 | a0001c0002t0015a0003c0009t0015 | 2 | HG03516.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*37C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 37 | chr12 | 53040260 | |||||
| chr12:53040321
|
C | A | 11 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(8): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*98C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 98 | chr12 | 53040321 | |||||
| chr12:53040477
|
G | A | 1 | a0001c0002t0011 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*254G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 254 | chr12 | 53040477 | |||||
| chr12:53040543
|
T | C | 1 | a0001c0002t0012 | 3 | HG00423.hp1 NA18990.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*320T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 320 | chr12 | 53040543 | |||||
| chr12:53040788
|
C | CT | 8 | a0001c0001t0002a0001c0001t0008a0001c0001t0024others(5): Show | 111 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*577dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 578 | INFO_REALIGN_3_PRIME | chr12 | 53040788 | ||||
| chr12:53040788
|
C | CTTT | 9 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(6): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*575_*577dupTTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 578 | INFO_REALIGN_3_PRIME | chr12 | 53040788 | ||||
| chr12:53040990
|
G | A | 1 | a0001c0001t0008 | 5 | HG02683.hp1 NA18944.hp1 NA18978.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*767G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 767 | chr12 | 53040990 | |||||
| chr12:53041006
|
C | T | 2 | a0001c0001t0017a0001c0001t0029 | 2 | HG00544.hp1 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*783C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 783 | chr12 | 53041006 | |||||
| chr12:53041127
|
T | C | 1 | a0001c0001t0024 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 904 | chr12 | 53041127 | |||||
| chr12:53041128
|
C | T | 1 | a0001c0001t0016 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 905 | chr12 | 53041128 | |||||
| chr12:53041129
|
A | G | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(22): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*906A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 906 | chr12 | 53041129 | |||||
| chr12:53041211
|
C | G | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*988C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 988 | chr12 | 53041211 | |||||
| chr12:53041240
|
C | T | 1 | a0001c0005t0013 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1017C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1017 | chr12 | 53041240 | |||||
| chr12:53041398
|
T | G | 1 | a0001c0001t0027 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1175 | chr12 | 53041398 | |||||
| chr12:53041458
|
A | G | 1 | a0001c0001t0014 | 2 | HG01256.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1235A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1235 | chr12 | 53041458 | |||||
| chr12:53041500
|
T | TTTG | 6 | a0001c0002t0004a0001c0002t0012a0001c0002t0015others(3): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1286_*1288dupGTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1289 | INFO_REALIGN_3_PRIME | chr12 | 53041500 | ||||
| chr12:53041509
|
G | GTTT | 24 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(21): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*1291_*1293dupTTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1294 | INFO_REALIGN_3_PRIME | chr12 | 53041509 | ||||
| chr12:53041509
|
G | T | 1 | a0001c0002t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1286G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1286 | chr12 | 53041509 | |||||
| chr12:53041575
|
T | C | 1 | a0001c0002t0011 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1352T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1352 | chr12 | 53041575 | |||||
| chr12:53041838
|
TAAG | T | 10 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(7): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1619_*1621delAAG | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1619 | INFO_REALIGN_3_PRIME | chr12 | 53041838 | ||||
| chr12:53041915
|
G | A | 1 | a0001c0001t0021 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1692 | chr12 | 53041915 | |||||
| chr12:53041952
|
A | G | 1 | a0001c0002t0019 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1729 | chr12 | 53041952 | |||||
| chr12:53041967
|
C | G | 1 | a0001c0001t0028 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1744C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1744 | chr12 | 53041967 | |||||
| chr12:53041978
|
T | C | 2 | a0001c0002t0003a0001c0002t0025 | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1755T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1755 | chr12 | 53041978 | |||||
| chr12:53041997
|
C | G | 2 | a0001c0001t0021a0001c0001t0023 | 2 | HG02451.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1774C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1774 | chr12 | 53041997 | |||||
| chr12:53042017
|
C | G | 1 | a0001c0002t0018 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1794C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1794 | chr12 | 53042017 | |||||
| chr12:53042112
|
T | C | 2 | a0001c0002t0007a0001c0002t0009 | 9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1889T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 15/15 | 1889 | chr12 | 53042112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53006656
|
T | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.13+160T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006656 | ||||||
| chr12:53006712
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.13+216C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006712 | ||||||
| chr12:53006785
|
G | A | 1 | a0001c0002t0007g0270 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.13+289G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006785 | ||||||
| chr12:53006913
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0012 | 2 | HG00642.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.13+417T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006913 | ||||||
| chr12:53006929
|
G | C | 1 | a0001c0002t0003g0271 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.13+433G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006929 | ||||||
| chr12:53006929
|
G | T | 1 | a0001c0002t0003g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.13+433G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006929 | ||||||
| chr12:53006944
|
A | T | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.13+448A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53006944 | ||||||
| chr12:53007062
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.13+566A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007062 | ||||||
| chr12:53007070
|
G | C | 1 | a0001c0005t0013g0272 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13+574G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007070 | ||||||
| chr12:53007122
|
C | T | 17 | a0001c0002t0003g0010a0001c0002t0003g0344a0001c0002t0003g0345others(14): Show | 18 | HG00544.hp2 NA18939.hp1 NA18950.hp2 others(15): Show |
intron_variant | MODIFIER | c.13+626C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007122 | ||||||
| chr12:53007224
|
T | C | 1 | a0001c0001t0002g0013 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.13+728T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007224 | ||||||
| chr12:53007233
|
G | A | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.13+737G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007233 | ||||||
| chr12:53007278
|
C | T | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.13+782C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007278 | ||||||
| chr12:53007310
|
A | G | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.13+814A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007310 | ||||||
| chr12:53007364
|
G | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.13+868G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007364 | ||||||
| chr12:53007420
|
C | CT | 39 | a0001c0002t0003g0320a0001c0002t0003g0356a0001c0002t0003g0357others(36): Show | 40 | HG00423.hp1 HG01109.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.13+952dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | |||||
| chr12:53007420
|
C | CTT | 17 | a0001c0002t0004g0005a0001c0002t0004g0300a0001c0002t0004g0301others(14): Show | 19 | HG02818.hp1 HG02895.hp1 HG02896.hp1 others(16): Show |
intron_variant | MODIFIER | c.13+951_13+952dupTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | |||||
| chr12:53007420
|
CT | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(147): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.13+952delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | |||||
| chr12:53007420
|
CTT | C | 9 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(6): Show | 9 | HG01070.hp2 HG01346.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+951_13+952delTT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53007420 | |||||
| chr12:53007444
|
T | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0014g0014 | 4 | HG01256.hp1 HG01258.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+948T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007444 | ||||||
| chr12:53007445
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(255): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.13+949T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007445 | ||||||
| chr12:53007445
|
T | TA | 5 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(2): Show | 5 | HG00558.hp1 HG02559.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.13+949_13+950insA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007445 | ||||||
| chr12:53007697
|
G | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(143): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.13+1201G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007697 | ||||||
| chr12:53007896
|
T | C | 11 | a0001c0002t0004g0274a0001c0002t0004g0282a0001c0002t0004g0283others(8): Show | 11 | HG00423.hp1 HG01255.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.13+1400T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007896 | ||||||
| chr12:53007934
|
G | C | 2 | a0001c0005t0013g0272a0001c0005t0013g0334 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.13+1438G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007934 | ||||||
| chr12:53007995
|
A | G | 1 | a0001c0002t0012g0290 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.13+1499A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53007995 | ||||||
| chr12:53008083
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.13+1587A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008083 | ||||||
| chr12:53008310
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.13+1814A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008310 | ||||||
| chr12:53008379
|
C | T | 1 | a0001c0001t0006g0037 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.13+1883C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008379 | ||||||
| chr12:53008711
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.13+2215G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008711 | ||||||
| chr12:53008986
|
G | A | 2 | a0001c0001t0021g0025a0001c0001t0023g0159 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.13+2490G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53008986 | ||||||
| chr12:53009083
|
A | G | 2 | a0001c0002t0015g0281a0003c0009t0015g0304 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.13+2587A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009083 | ||||||
| chr12:53009149
|
C | A | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.13+2653C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009149 | ||||||
| chr12:53009162
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.13+2666A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009162 | ||||||
| chr12:53009164
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.13+2668T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009164 | ||||||
| chr12:53009204
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.13+2708G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009204 | ||||||
| chr12:53009243
|
G | A | 1 | a0001c0002t0004g0275 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.13+2747G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009243 | ||||||
| chr12:53009329
|
G | T | 1 | a0001c0001t0002g0251 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.13+2833G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009329 | ||||||
| chr12:53009399
|
G | A | 1 | a0001c0001t0002g0160 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.13+2903G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009399 | ||||||
| chr12:53009474
|
G | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0267 | 2 | HG02559.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.13+2978G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009474 | ||||||
| chr12:53009489
|
C | T | 9 | a0001c0002t0007g0270a0001c0002t0007g0336a0001c0002t0007g0337others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+2993C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009489 | ||||||
| chr12:53009494
|
C | CA | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(262): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.13+3010dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53009494 | |||||
| chr12:53009494
|
CAAAAAA | C | 31 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(28): Show | 32 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.13+3005_13+3010del others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53009494 | |||||
| chr12:53009507
|
C | A | 1 | a0001c0001t0002g0161 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.13+3011C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009507 | ||||||
| chr12:53009586
|
A | C | 2 | a0001c0002t0004g0299a0001c0002t0004g0303 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.13+3090A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009586 | ||||||
| chr12:53009639
|
G | A | 1 | a0001c0002t0004g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13+3143G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009639 | ||||||
| chr12:53009740
|
T | C | 1 | a0001c0002t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.13+3244T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009740 | ||||||
| chr12:53009796
|
T | C | 3 | a0001c0001t0021g0025a0001c0001t0023g0159a0001c0002t0004g0300 | 3 | HG02451.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.13+3300T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009796 | ||||||
| chr12:53009837
|
A | T | 3 | a0001c0002t0004g0296a0001c0002t0004g0297a0001c0002t0004g0298 | 3 | HG01167.hp1 HG01169.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.13+3341A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009837 | ||||||
| chr12:53009864
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.13+3368T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009864 | ||||||
| chr12:53009934
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.13+3438T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53009934 | ||||||
| chr12:53010037
|
T | C | 346 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(343): Show | 355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.13+3541T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010037 | ||||||
| chr12:53010137
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.13+3641A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010137 | ||||||
| chr12:53010151
|
T | C | 1 | a0001c0002t0018g0292 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.13+3655T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010151 | ||||||
| chr12:53010392
|
G | A | 2 | a0001c0002t0004g0282a0001c0002t0004g0283 | 2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.13+3896G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010392 | ||||||
| chr12:53010399
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.13+3903C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010399 | ||||||
| chr12:53010454
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.13+3958A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010454 | ||||||
| chr12:53010564
|
C | CTGTT | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.13+4070_13+4071ins others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53010564 | |||||
| chr12:53010727
|
A | G | 1 | a0001c0002t0004g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.13+4231A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010727 | ||||||
| chr12:53010754
|
C | T | 1 | a0001c0002t0005g0008 | 2 | HG01109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.13+4258C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010754 | ||||||
| chr12:53010872
|
C | A | 79 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0017others(76): Show | 79 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.13+4376C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010872 | ||||||
| chr12:53010916
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.13+4420T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53010916 | ||||||
| chr12:53011289
|
C | T | 1 | a0001c0002t0025g0355 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.13+4793C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011289 | ||||||
| chr12:53011467
|
C | A | 4 | a0001c0002t0004g0284a0001c0002t0012g0273a0001c0002t0012g0285others(1): Show | 4 | HG00423.hp1 HG02165.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+4971C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011467 | ||||||
| chr12:53011502
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0268 | 2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.14-4971T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011502 | ||||||
| chr12:53011537
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.14-4936A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011537 | ||||||
| chr12:53011598
|
C | T | 2 | a0001c0002t0004g0275a0001c0002t0004g0280 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.14-4875C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011598 | ||||||
| chr12:53011613
|
C | G | 1 | a0001c0002t0003g0316 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.14-4860C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53011613 | ||||||
| chr12:53012101
|
G | A | 1 | a0001c0002t0003g0311 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.14-4372G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012101 | ||||||
| chr12:53012319
|
CAG | C | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(259): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.14-4151_14-4150del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53012319 | |||||
| chr12:53012321
|
G | C | 1 | a0001c0001t0002g0163 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.14-4152G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012321 | ||||||
| chr12:53012370
|
C | G | 3 | a0001c0002t0009g0318a0001c0002t0009g0319a0001c0002t0009g0341 | 3 | HG01884.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.14-4103C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012370 | ||||||
| chr12:53012429
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.14-4044C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012429 | ||||||
| chr12:53012469
|
G | A | 1 | a0001c0001t0002g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.14-4004G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012469 | ||||||
| chr12:53012478
|
C | T | 2 | a0001c0002t0015g0281a0003c0009t0015g0304 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.14-3995C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012478 | ||||||
| chr12:53012503
|
G | A | 1 | a0001c0005t0005g0009 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.14-3970G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012503 | ||||||
| chr12:53012567
|
C | T | 1 | a0001c0002t0004g0279 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.14-3906C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012567 | ||||||
| chr12:53012569
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.14-3904T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012569 | ||||||
| chr12:53012597
|
C | CT | 6 | a0001c0002t0003g0358a0001c0002t0004g0289a0001c0002t0005g0332others(3): Show | 6 | HG02055.hp2 HG03516.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.14-3863dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53012597 | |||||
| chr12:53012614
|
T | C | 1 | a0001c0001t0002g0164 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.14-3859T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012614 | ||||||
| chr12:53012629
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.14-3844G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012629 | ||||||
| chr12:53012669
|
G | A | 31 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(28): Show | 32 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.14-3804G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012669 | ||||||
| chr12:53012796
|
C | T | 27 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(24): Show | 30 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.14-3677C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012796 | ||||||
| chr12:53012827
|
C | T | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-3646C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012827 | ||||||
| chr12:53012874
|
G | T | 1 | a0001c0001t0002g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.14-3599G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012874 | ||||||
| chr12:53012881
|
C | T | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-3592C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53012881 | ||||||
| chr12:53013054
|
A | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(152): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.14-3419A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013054 | ||||||
| chr12:53013228
|
A | G | 3 | a0001c0001t0001g0104a0002c0004t0001g0103a0002c0004t0001g0105 | 3 | HG01257.hp1 HG01258.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.14-3245A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013228 | ||||||
| chr12:53013256
|
G | A | 1 | a0001c0001t0022g0263 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.14-3217G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013256 | ||||||
| chr12:53013263
|
C | A | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG01081.hp2 HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.14-3210C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013263 | ||||||
| chr12:53013783
|
T | TA | 55 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 58 | HG00423.hp2 HG00544.hp2 HG01261.hp2 others(55): Show |
intron_variant | MODIFIER | c.14-2675dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53013783 | |||||
| chr12:53013885
|
A | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.14-2588A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013885 | ||||||
| chr12:53013904
|
T | C | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.14-2569T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013904 | ||||||
| chr12:53013920
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.14-2553G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53013920 | ||||||
| chr12:53014065
|
A | G | 108 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(105): Show | 110 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.14-2408A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014065 | ||||||
| chr12:53014157
|
C | T | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.14-2316C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014157 | ||||||
| chr12:53014160
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.14-2313G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014160 | ||||||
| chr12:53014246
|
TA | T | 9 | a0001c0001t0001g0102a0001c0001t0001g0155a0001c0001t0002g0243others(6): Show | 9 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.14-2211delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53014246 | |||||
| chr12:53014285
|
G | A | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.14-2188G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014285 | ||||||
| chr12:53014381
|
C | G | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.14-2092C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014381 | ||||||
| chr12:53014412
|
C | CA | 15 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0110others(12): Show | 16 | HG01358.hp1 HG01358.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.14-2045dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53014412 | |||||
| chr12:53014603
|
T | G | 6 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0309others(3): Show | 8 | HG02071.hp1 HG02083.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.14-1870T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014603 | ||||||
| chr12:53014739
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.14-1734T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014739 | ||||||
| chr12:53014796
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(150): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.14-1677A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014796 | ||||||
| chr12:53014869
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.14-1604G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014869 | ||||||
| chr12:53014900
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.14-1573C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53014900 | ||||||
| chr12:53015116
|
A | G | 1 | a0001c0002t0007g0340 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.14-1357A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015116 | ||||||
| chr12:53015141
|
T | C | 1 | a0001c0001t0006g0016 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.14-1332T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015141 | ||||||
| chr12:53015273
|
G | A | 6 | a0001c0002t0004g0275a0001c0002t0004g0277a0001c0002t0004g0280others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-1200G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015273 | ||||||
| chr12:53015309
|
C | T | 1 | a0001c0007t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.14-1164C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015309 | ||||||
| chr12:53015470
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.14-1003G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015470 | ||||||
| chr12:53015526
|
T | C | 4 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-947T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015526 | ||||||
| chr12:53015630
|
G | A | 1 | a0001c0002t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.14-843G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015630 | ||||||
| chr12:53015680
|
C | CA | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(250): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.14-781dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015680 | |||||
| chr12:53015680
|
C | CAA | 10 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0119others(7): Show | 10 | HG00735.hp1 HG01255.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.14-782_14-781dupAA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015680 | |||||
| chr12:53015709
|
G | A | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG02698.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.14-764G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015709 | ||||||
| chr12:53015718
|
C | T | 2 | a0001c0002t0004g0291a0001c0002t0018g0292 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.14-755C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015718 | ||||||
| chr12:53015806
|
G | A | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.14-667G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53015806 | ||||||
| chr12:53015978
|
C | CAA | 27 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0271others(24): Show | 29 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.14-479_14-478dupAA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015978 | |||||
| chr12:53015978
|
CA | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.14-478delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr12 | 53015978 | |||||
| chr12:53016266
|
CAT | C | 108 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(105): Show | 110 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.14-206_14-205delAT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 1/14 | chr12 | 53016266 | ||||||
| chr12:53017252
|
CA | C | 34 | a0001c0001t0021g0025a0001c0001t0023g0159a0001c0002t0003g0006others(31): Show | 37 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.151+657delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 53017252 | |||||
| chr12:53017252
|
CAA | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.151+656_151+657del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 53017252 | |||||
| chr12:53017295
|
A | G | 8 | a0001c0001t0001g0100a0001c0001t0006g0016a0001c0002t0004g0284others(5): Show | 8 | HG00423.hp1 HG01070.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+685A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017295 | ||||||
| chr12:53017348
|
CAG | C | 3 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0251 | 3 | HG02015.hp1 HG02074.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.151+741_151+742del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr12 | 53017348 | |||||
| chr12:53017518
|
C | T | 6 | a0001c0002t0004g0284a0001c0002t0004g0287a0001c0002t0004g0288others(3): Show | 6 | HG00423.hp1 HG02040.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+908C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017518 | ||||||
| chr12:53017697
|
G | A | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.151+1087G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017697 | ||||||
| chr12:53017748
|
C | T | 2 | a0001c0002t0004g0291a0001c0002t0018g0292 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.152-1050C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017748 | ||||||
| chr12:53017938
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.152-860C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53017938 | ||||||
| chr12:53018174
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.152-624A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018174 | ||||||
| chr12:53018194
|
A | G | 1 | a0001c0002t0004g0286 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.152-604A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018194 | ||||||
| chr12:53018238
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.152-560T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018238 | ||||||
| chr12:53018383
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.152-415T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018383 | ||||||
| chr12:53018526
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.152-272A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018526 | ||||||
| chr12:53018538
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.152-260G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018538 | ||||||
| chr12:53018543
|
T | C | 25 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(22): Show | 28 | HG00544.hp2 HG02071.hp1 HG02083.hp2 others(25): Show |
intron_variant | MODIFIER | c.152-255T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018543 | ||||||
| chr12:53018678
|
T | C | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.152-120T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018678 | ||||||
| chr12:53018702
|
A | G | 21 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0040others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.152-96A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018702 | ||||||
| chr12:53018753
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.152-45G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 2/14 | chr12 | 53018753 | ||||||
| chr12:53019134
|
C | G | 1 | a0001c0001t0001g0086 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.360+128C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019134 | ||||||
| chr12:53019147
|
C | G | 1 | a0001c0002t0003g0307 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.360+141C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019147 | ||||||
| chr12:53019423
|
TTA | T | 6 | a0001c0001t0002g0171a0001c0001t0002g0176a0001c0001t0002g0177others(3): Show | 6 | HG00609.hp1 HG02717.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+431_360+432del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019423 | |||||
| chr12:53019423
|
TTATA | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0126a0001c0001t0001g0135others(5): Show | 8 | HG01074.hp2 HG01123.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+429_360+432del others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019423 | |||||
| chr12:53019432
|
TATA | T | 41 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0022others(38): Show | 42 | HG00438.hp1 HG00609.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.360+427_360+429del others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019432 | ||||||
| chr12:53019433
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0072 | 2 | NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.360+428_360+429ins others(10): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019433 | |||||
| chr12:53019433
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0077 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.360+428_360+429ins others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019433 | |||||
| chr12:53019433
|
A | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0085 | 3 | HG01167.hp2 HG01169.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.360+427A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019433 | ||||||
| chr12:53019434
|
TATA | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0106others(40): Show | 44 | HG00140.hp2 HG01081.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.360+429_360+431del others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019434 | ||||||
| chr12:53019435
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.360+429A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019435 | ||||||
| chr12:53019435
|
A | T | 76 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(73): Show | 76 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.360+429A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019435 | ||||||
| chr12:53019436
|
T | TTTTTTTT others(4): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(2): Show | 5 | HG02040.hp1 NA18948.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+430_360+431ins others(11): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019436 | ||||||
| chr12:53019436
|
TA | T | 73 | a0001c0001t0002g0004a0001c0001t0002g0013a0001c0001t0002g0026others(70): Show | 75 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.360+431delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019436 | ||||||
| chr12:53019437
|
A | ATATATTT others(9): Show |
6 | a0001c0002t0003g0309a0001c0002t0003g0313a0001c0002t0003g0314others(3): Show | 6 | HG02071.hp1 HG02523.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATATTT others(10): Show |
9 | a0001c0002t0003g0311a0001c0002t0003g0320a0001c0002t0003g0344others(6): Show | 9 | HG00544.hp2 NA18950.hp2 NA18992.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATATTT others(11): Show |
4 | a0001c0002t0003g0010a0001c0002t0003g0316a0001c0002t0003g0349others(1): Show | 5 | HG02083.hp2 NA18939.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATTTTT others(8): Show |
1 | a0001c0002t0003g0306 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.360+432_360+433ins others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATTTTT others(9): Show |
3 | a0001c0002t0003g0305a0001c0002t0003g0307a0001c0002t0003g0350 | 3 | NA18975.hp1 NA18993.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.360+432_360+433ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATTTTT others(10): Show |
2 | a0001c0002t0003g0006a0001c0002t0003g0357 | 3 | NA18944.hp2 NA18967.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.360+432_360+433ins others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATTTTT others(11): Show |
4 | a0001c0002t0003g0007a0001c0002t0003g0271a0001c0002t0003g0310others(1): Show | 5 | HG00423.hp2 HG01099.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATTTTT others(12): Show |
1 | a0001c0002t0003g0351 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.360+432_360+433ins others(19): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | ATATTTTT others(13): Show |
1 | a0001c0002t0003g0352 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.360+432_360+433ins others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019437 | |||||
| chr12:53019437
|
A | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0072 | 2 | NA18991.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.360+431A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019437 | ||||||
| chr12:53019437
|
A | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(138): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.360+431A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019437 | ||||||
| chr12:53019438
|
T | TA | 5 | a0001c0002t0005g0008a0001c0002t0005g0324a0001c0002t0005g0331others(2): Show | 6 | HG01109.hp1 HG02109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+432_360+433ins others(1): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019438 | ||||||
| chr12:53019439
|
T | A | 16 | a0001c0002t0004g0005a0001c0002t0004g0276a0001c0002t0004g0279others(13): Show | 17 | HG01891.hp1 HG02572.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.360+433T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019439 | ||||||
| chr12:53019440
|
T | TTTTTTTC | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0021others(11): Show | 14 | HG01952.hp2 HG01975.hp1 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(7): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019440 | |||||
| chr12:53019441
|
T | A | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.360+435T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019441 | ||||||
| chr12:53019441
|
T | TTTTTTC | 11 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(8): Show | 11 | HG01070.hp2 HG01106.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019441 | |||||
| chr12:53019442
|
T | TTTTTC | 7 | a0001c0001t0001g0043a0001c0001t0001g0055a0001c0001t0001g0085others(4): Show | 7 | HG01167.hp2 HG01358.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019442 | |||||
| chr12:53019443
|
T | A | 1 | a0001c0002t0011g0359 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.360+437T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019443 | ||||||
| chr12:53019443
|
T | TTTTC | 23 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0040others(20): Show | 23 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.360+440_360+441ins others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019443 | |||||
| chr12:53019446
|
T | C | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.360+440T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019446 | ||||||
| chr12:53019447
|
T | C | 7 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0175others(4): Show | 7 | HG00438.hp2 HG02723.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+441T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019447 | ||||||
| chr12:53019448
|
T | C | 83 | a0001c0001t0002g0004a0001c0001t0002g0013a0001c0001t0002g0026others(80): Show | 84 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.360+442T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019448 | ||||||
| chr12:53019449
|
T | C | 13 | a0001c0001t0001g0024a0001c0001t0006g0032a0001c0001t0006g0037others(10): Show | 13 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+443T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019449 | ||||||
| chr12:53019449
|
TC | T | 8 | a0001c0001t0002g0170a0001c0001t0002g0175a0001c0002t0007g0336others(5): Show | 8 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.360+444delC | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019449 | ||||||
| chr12:53019450
|
C | CT | 22 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0124others(19): Show | 22 | HG00423.hp1 HG00438.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.361-436dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019450 | |||||
| chr12:53019450
|
C | CTTTTTTT others(8): Show |
1 | a0001c0002t0003g0308 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.361-450_361-436dup others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019450 | |||||
| chr12:53019450
|
C | T | 211 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0017others(208): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.360+444C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019450 | ||||||
| chr12:53019450
|
CT | C | 6 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(3): Show | 6 | HG00140.hp2 HG02258.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-436delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019450 | |||||
| chr12:53019453
|
T | C | 1 | a0001c0007t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.360+447T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019453 | ||||||
| chr12:53019454
|
T | C | 1 | a0001c0002t0003g0344 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.360+448T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019454 | ||||||
| chr12:53019456
|
T | C | 5 | a0001c0001t0002g0169a0001c0001t0002g0225a0001c0001t0002g0226others(2): Show | 5 | HG00438.hp2 HG03831.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+450T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019456 | ||||||
| chr12:53019457
|
T | C | 82 | a0001c0001t0002g0004a0001c0001t0002g0013a0001c0001t0002g0026others(79): Show | 83 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.360+451T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019457 | ||||||
| chr12:53019457
|
T | TTC | 23 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0172others(20): Show | 23 | HG02015.hp1 HG02074.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.360+452_361-451ins others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019457 | |||||
| chr12:53019458
|
T | TC | 3 | a0001c0001t0002g0003a0001c0001t0002g0162a0001c0001t0002g0268 | 4 | HG01934.hp1 HG01975.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+452_361-451ins others(1): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019458 | ||||||
| chr12:53019641
|
C | T | 110 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(107): Show | 112 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.361-269C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019641 | ||||||
| chr12:53019653
|
A | G | 1 | a0001c0001t0002g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.361-257A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019653 | ||||||
| chr12:53019675
|
C | CT | 113 | a0001c0001t0001g0017a0001c0001t0001g0073a0001c0001t0001g0139others(110): Show | 115 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.361-218dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019675 | |||||
| chr12:53019675
|
C | CTT | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(134): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.361-219_361-218dup others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019675 | |||||
| chr12:53019675
|
C | CTTT | 6 | a0001c0001t0001g0023a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01074.hp2 HG01978.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-220_361-218dup others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr12 | 53019675 | |||||
| chr12:53019754
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-156A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 3/14 | chr12 | 53019754 | ||||||
| chr12:53020223
|
C | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG02027.hp2 HG02155.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+197C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020223 | ||||||
| chr12:53020226
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.477+200A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020226 | ||||||
| chr12:53020266
|
A | T | 1 | a0001c0002t0003g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.477+240A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020266 | ||||||
| chr12:53020542
|
A | G | 2 | a0001c0002t0015g0281a0003c0009t0015g0304 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.477+516A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020542 | ||||||
| chr12:53020654
|
A | G | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.477+628A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020654 | ||||||
| chr12:53020907
|
G | A | 3 | a0001c0002t0004g0275a0001c0002t0004g0277a0001c0002t0004g0280 | 3 | HG02572.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.477+881G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020907 | ||||||
| chr12:53020985
|
A | C | 2 | a0001c0001t0002g0221a0001c0001t0002g0222 | 2 | NA19002.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.478-821A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020985 | ||||||
| chr12:53020988
|
G | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.478-818G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53020988 | ||||||
| chr12:53021255
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.478-551A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021255 | ||||||
| chr12:53021350
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.478-456T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021350 | ||||||
| chr12:53021565
|
G | T | 1 | a0001c0007t0001g0101 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.478-241G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021565 | ||||||
| chr12:53021622
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.478-184T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021622 | ||||||
| chr12:53021664
|
A | G | 2 | a0001c0002t0004g0291a0001c0002t0018g0292 | 2 | HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.478-142A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021664 | ||||||
| chr12:53021732
|
A | C | 2 | a0001c0001t0002g0218a0001c0001t0002g0219 | 2 | HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.478-74A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 4/14 | chr12 | 53021732 | ||||||
| chr12:53022216
|
G | A | 1 | a0001c0001t0008g0183 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.533-277G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022216 | ||||||
| chr12:53022291
|
A | T | 1 | a0001c0001t0014g0071 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.533-202A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022291 | ||||||
| chr12:53022335
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.533-158T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022335 | ||||||
| chr12:53022338
|
A | C | 25 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0276others(22): Show | 26 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.533-155A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022338 | ||||||
| chr12:53022467
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.533-26C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022467 | ||||||
| chr12:53022479
|
T | C | 1 | a0001c0002t0003g0307 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.533-14T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 5/14 | chr12 | 53022479 | ||||||
| chr12:53022841
|
G | A | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.667+214G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53022841 | ||||||
| chr12:53022915
|
A | G | 109 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(106): Show | 111 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.667+288A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53022915 | ||||||
| chr12:53022989
|
C | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0064 | 2 | NA19083.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.667+362C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53022989 | ||||||
| chr12:53023023
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.667+396G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023023 | ||||||
| chr12:53023271
|
C | T | 1 | a0001c0002t0004g0279 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.667+644C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023271 | ||||||
| chr12:53023313
|
A | G | 3 | a0001c0001t0002g0217a0001c0001t0002g0239a0001c0001t0002g0240 | 3 | HG01106.hp2 HG03490.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.667+686A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023313 | ||||||
| chr12:53023378
|
G | A | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.667+751G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023378 | ||||||
| chr12:53023381
|
C | T | 4 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+754C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023381 | ||||||
| chr12:53023420
|
A | C | 1 | a0001c0002t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.667+793A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023420 | ||||||
| chr12:53023420
|
A | G | 1 | a0001c0002t0004g0289 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.667+793A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023420 | ||||||
| chr12:53023437
|
T | TGGCCAGG others(20): Show |
1 | a0001c0002t0004g0284 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.667+811_667+837dup others(27): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023437 | |||||
| chr12:53023463
|
C | G | 1 | a0001c0002t0003g0310 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.667+836C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023463 | ||||||
| chr12:53023578
|
A | AT | 22 | a0001c0001t0001g0021a0001c0001t0001g0049a0001c0001t0001g0063others(19): Show | 22 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.667+973dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | |||||
| chr12:53023578
|
A | ATT | 101 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(98): Show | 104 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.667+972_667+973dup others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | |||||
| chr12:53023578
|
A | ATTT | 41 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0002g0182others(38): Show | 44 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.667+971_667+973dup others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | |||||
| chr12:53023578
|
A | ATTTT | 7 | a0001c0001t0002g0244a0001c0002t0003g0305a0001c0002t0003g0308others(4): Show | 7 | HG02056.hp1 HG02083.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.667+970_667+973dup others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | |||||
| chr12:53023578
|
AT | A | 13 | a0001c0001t0001g0024a0001c0001t0001g0087a0001c0001t0001g0127others(10): Show | 13 | HG01070.hp1 HG01515.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.667+973delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53023578 | |||||
| chr12:53023617
|
C | G | 2 | a0001c0002t0004g0299a0001c0002t0004g0303 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.667+990C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023617 | ||||||
| chr12:53023686
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.667+1059C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023686 | ||||||
| chr12:53023763
|
A | T | 1 | a0001c0002t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.667+1136A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023763 | ||||||
| chr12:53023802
|
C | T | 1 | a0001c0002t0004g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.667+1175C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023802 | ||||||
| chr12:53023919
|
C | A | 1 | a0001c0001t0001g0015 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.667+1292C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023919 | ||||||
| chr12:53023964
|
G | C | 2 | a0001c0001t0006g0033a0001c0001t0006g0036 | 2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.667+1337G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53023964 | ||||||
| chr12:53024047
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0065a0001c0001t0001g0078others(2): Show | 5 | HG01952.hp2 HG01975.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.667+1420G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024047 | ||||||
| chr12:53024097
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.667+1470C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024097 | ||||||
| chr12:53024199
|
T | C | 1 | a0001c0001t0006g0032 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.667+1572T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024199 | ||||||
| chr12:53024314
|
A | T | 1 | a0001c0002t0004g0274 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.667+1687A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024314 | ||||||
| chr12:53024315
|
TAAC | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG00140.hp2 HG01081.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.667+1693_667+1695d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53024315 | |||||
| chr12:53024408
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG00140.hp2 HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.667+1781G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024408 | ||||||
| chr12:53024429
|
G | A | 107 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(104): Show | 109 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.667+1802G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024429 | ||||||
| chr12:53024448
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.667+1821C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024448 | ||||||
| chr12:53024467
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.667+1840A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024467 | ||||||
| chr12:53024490
|
C | G | 1 | a0001c0001t0001g0039 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.667+1863C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024490 | ||||||
| chr12:53024510
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.667+1883A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024510 | ||||||
| chr12:53024648
|
CTTTGTTT others(3): Show |
C | 6 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.667+2041_667+2050d others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53024648 | |||||
| chr12:53024791
|
G | T | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.667+2164G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024791 | ||||||
| chr12:53024800
|
T | C | 1 | a0001c0001t0002g0251 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.667+2173T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024800 | ||||||
| chr12:53024946
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.667+2319G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53024946 | ||||||
| chr12:53025453
|
A | C | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.668-2329A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025453 | ||||||
| chr12:53025654
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.668-2128T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025654 | ||||||
| chr12:53025827
|
G | T | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-1955G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025827 | ||||||
| chr12:53025831
|
G | T | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-1951G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025831 | ||||||
| chr12:53025974
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0133a0001c0001t0001g0262 | 3 | HG03831.hp1 HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.668-1808G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53025974 | ||||||
| chr12:53026066
|
C | G | 1 | a0001c0001t0001g0257 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.668-1716C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026066 | ||||||
| chr12:53026144
|
A | G | 1 | a0001c0002t0004g0274 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.668-1638A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026144 | ||||||
| chr12:53026267
|
C | G | 1 | a0001c0003t0005g0327 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.668-1515C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026267 | ||||||
| chr12:53026435
|
AAAC | A | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-1342_668-1340d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53026435 | |||||
| chr12:53026496
|
C | T | 1 | a0001c0002t0003g0344 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.668-1286C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026496 | ||||||
| chr12:53026497
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.668-1285A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026497 | ||||||
| chr12:53026602
|
GATTT | G | 3 | a0001c0002t0004g0275a0001c0002t0004g0277a0001c0002t0004g0280 | 3 | HG02572.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.668-1167_668-1164d others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53026602 | |||||
| chr12:53026606
|
T | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.668-1176T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026606 | ||||||
| chr12:53026726
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.668-1056C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026726 | ||||||
| chr12:53026840
|
C | G | 3 | a0001c0001t0002g0028a0001c0001t0002g0212a0001c0001t0002g0220 | 3 | HG00735.hp2 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.668-942C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026840 | ||||||
| chr12:53026841
|
A | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.668-941A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026841 | ||||||
| chr12:53026879
|
A | C | 3 | a0001c0001t0002g0160a0001c0001t0002g0164a0001c0001t0027g0184 | 3 | HG01891.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.668-903A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026879 | ||||||
| chr12:53026879
|
A | G | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(294): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.668-903A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53026879 | ||||||
| chr12:53027124
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.668-658A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027124 | ||||||
| chr12:53027136
|
A | ATTT | 3 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0251 | 3 | HG02015.hp1 HG02074.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.668-646_668-645ins others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0141 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.668-646_668-645ins others(10): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0002g0170a0001c0001t0002g0185 | 2 | NA18965.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.668-646_668-645ins others(11): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(5): Show |
23 | a0001c0001t0002g0013a0001c0001t0002g0164a0001c0001t0002g0171others(20): Show | 23 | HG00609.hp1 HG00642.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(6): Show |
34 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0026others(31): Show | 36 | HG00438.hp2 HG00544.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(13): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(7): Show |
19 | a0001c0001t0002g0027a0001c0001t0002g0029a0001c0001t0002g0163others(16): Show | 19 | HG00558.hp1 HG00558.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(14): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(8): Show |
17 | a0001c0001t0001g0255a0001c0001t0002g0030a0001c0001t0002g0180others(14): Show | 17 | HG01106.hp2 HG01952.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(9): Show |
6 | a0001c0001t0001g0254a0001c0001t0002g0028a0001c0001t0002g0173others(3): Show | 6 | HG02300.hp1 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(10): Show |
10 | a0001c0001t0001g0080a0001c0001t0001g0142a0001c0001t0001g0261others(7): Show | 10 | HG02129.hp1 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(11): Show |
22 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0051others(19): Show | 23 | HG01070.hp1 HG01070.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(12): Show |
56 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0023others(53): Show | 56 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(19): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(13): Show |
42 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(39): Show | 43 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(14): Show |
14 | a0001c0001t0001g0024a0001c0001t0001g0072a0001c0001t0001g0094others(11): Show | 14 | HG00140.hp2 HG00438.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(21): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(15): Show |
6 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0113others(3): Show | 6 | HG02056.hp2 HG03239.hp1 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.668-646_668-645ins others(22): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.668-646_668-645ins others(23): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0001g0061 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.668-646_668-645ins others(24): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.668-646_668-645ins others(25): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(19): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0055 | 2 | HG01358.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.668-646_668-645ins others(26): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027136
|
A | ATTTTTTT others(21): Show |
1 | a0001c0001t0001g0114 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.668-646_668-645ins others(28): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027136 | ||||||
| chr12:53027137
|
A | AAATTTTT others(6): Show |
1 | a0001c0002t0003g0305 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.668-645_668-644ins others(13): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | ||||||
| chr12:53027137
|
A | AAATTTTT others(9): Show |
1 | a0001c0002t0003g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.668-645_668-644ins others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | ||||||
| chr12:53027137
|
A | AATTTTTT others(3): Show |
2 | a0001c0002t0003g0306a0001c0002t0003g0315 | 2 | HG01099.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.668-645_668-644ins others(10): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | ||||||
| chr12:53027137
|
A | AATTTTTT others(4): Show |
18 | a0001c0002t0003g0007a0001c0002t0003g0010a0001c0002t0003g0271others(15): Show | 20 | HG00423.hp2 HG00544.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.668-645_668-644ins others(11): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | ||||||
| chr12:53027137
|
A | AATTTTTT others(5): Show |
11 | a0001c0002t0003g0006a0001c0002t0003g0311a0001c0002t0003g0314others(8): Show | 12 | HG02071.hp1 HG02083.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.668-645_668-644ins others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | ||||||
| chr12:53027137
|
A | AT | 14 | a0001c0002t0004g0282a0001c0002t0004g0288a0001c0002t0004g0289others(11): Show | 14 | HG02040.hp2 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.668-625dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | |||||
| chr12:53027137
|
A | ATTTTTTT others(7): Show |
2 | a0001c0002t0011g0360a0001c0002t0011g0361 | 2 | HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.668-638_668-625dup others(14): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | |||||
| chr12:53027137
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.668-644_668-625dup others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | |||||
| chr12:53027137
|
A | ATTTTTTT others(15): Show |
1 | a0001c0002t0011g0359 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.668-625_668-624ins others(22): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr12 | 53027137 | |||||
| chr12:53027137
|
A | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(258): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.668-645A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027137 | ||||||
| chr12:53027193
|
C | T | 4 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361others(1): Show | 4 | HG01891.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-589C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027193 | ||||||
| chr12:53027279
|
G | A | 2 | a0001c0001t0021g0025a0001c0001t0023g0159 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.668-503G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027279 | ||||||
| chr12:53027322
|
C | G | 4 | a0001c0002t0004g0284a0001c0002t0012g0273a0001c0002t0012g0285others(1): Show | 4 | HG00423.hp1 HG02165.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.668-460C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027322 | ||||||
| chr12:53027323
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.668-459G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027323 | ||||||
| chr12:53027343
|
A | T | 31 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(28): Show | 32 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.668-439A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027343 | ||||||
| chr12:53027345
|
G | A | 2 | a0001c0001t0021g0025a0001c0001t0023g0159 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.668-437G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027345 | ||||||
| chr12:53027354
|
G | A | 9 | a0001c0002t0007g0270a0001c0002t0007g0336a0001c0002t0007g0337others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.668-428G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027354 | ||||||
| chr12:53027624
|
T | G | 2 | a0001c0001t0021g0025a0001c0001t0023g0159 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.668-158T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027624 | ||||||
| chr12:53027723
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.668-59G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 6/14 | chr12 | 53027723 | ||||||
| chr12:53027962
|
CT | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.806-43delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 53027962 | |||||
| chr12:53028261
|
C | T | 2 | a0001c0002t0004g0276a0001c0002t0005g0335 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.979+73C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028261 | ||||||
| chr12:53028346
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.979+158T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028346 | ||||||
| chr12:53028447
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.979+259A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028447 | ||||||
| chr12:53028556
|
C | CA | 6 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0060others(3): Show | 6 | HG02027.hp2 NA18939.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.979+383dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53028556 | |||||
| chr12:53028742
|
G | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.979+554G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028742 | ||||||
| chr12:53028820
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.979+632A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028820 | ||||||
| chr12:53028834
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.979+646G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53028834 | ||||||
| chr12:53029083
|
C | G | 1 | a0001c0002t0003g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.979+895C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029083 | ||||||
| chr12:53029094
|
C | A | 1 | a0001c0001t0002g0028 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.979+906C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029094 | ||||||
| chr12:53029120
|
C | CA | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(257): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.979+944dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53029120 | |||||
| chr12:53029137
|
T | C | 2 | a0001c0002t0004g0296a0001c0002t0004g0297 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.979+949T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029137 | ||||||
| chr12:53029177
|
A | G | 1 | a0001c0002t0019g0278 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.979+989A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029177 | ||||||
| chr12:53029204
|
C | T | 1 | a0001c0002t0018g0292 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.979+1016C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029204 | ||||||
| chr12:53029220
|
C | T | 1 | a0001c0001t0006g0037 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.979+1032C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029220 | ||||||
| chr12:53029239
|
T | C | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.979+1051T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029239 | ||||||
| chr12:53029274
|
T | C | 109 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(106): Show | 111 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.979+1086T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029274 | ||||||
| chr12:53029375
|
TTA | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(282): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.979+1189_979+1190d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53029375 | |||||
| chr12:53029376
|
TA | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0108a0001c0001t0001g0155others(7): Show | 10 | HG01070.hp2 HG01981.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.979+1189delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029376 | ||||||
| chr12:53029377
|
A | T | 2 | a0001c0002t0003g0362a0001c0002t0020g0342 | 2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.979+1189A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029377 | ||||||
| chr12:53029380
|
T | A | 1 | a0001c0001t0002g0195 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.979+1192T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029380 | ||||||
| chr12:53029395
|
C | T | 1 | a0001c0002t0004g0276 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.979+1207C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029395 | ||||||
| chr12:53029532
|
T | C | 1 | a0001c0001t0029g0196 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.979+1344T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029532 | ||||||
| chr12:53029609
|
C | T | 4 | a0001c0005t0005g0009a0001c0005t0013g0272a0001c0005t0013g0312others(1): Show | 5 | HG02970.hp2 HG06807.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+1421C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029609 | ||||||
| chr12:53029654
|
A | G | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(330): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.979+1466A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029654 | ||||||
| chr12:53029695
|
T | A | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.979+1507T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029695 | ||||||
| chr12:53029709
|
C | T | 33 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(30): Show | 36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.979+1521C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029709 | ||||||
| chr12:53029721
|
G | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.979+1533G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029721 | ||||||
| chr12:53029856
|
C | T | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.979+1668C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53029856 | ||||||
| chr12:53029927
|
T | TA | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(268): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.979+1747dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53029927 | |||||
| chr12:53030009
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.979+1821T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030009 | ||||||
| chr12:53030021
|
A | G | 2 | a0001c0001t0021g0025a0001c0001t0023g0159 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.979+1833A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030021 | ||||||
| chr12:53030031
|
TGGCAACA others(151): Show |
T | 11 | a0001c0001t0001g0024a0001c0001t0001g0072a0001c0001t0001g0095others(8): Show | 11 | HG01123.hp1 HG03710.hp1 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+1879_979+2036d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030031 | |||||
| chr12:53030043
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | HG02027.hp2 HG02155.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+1855G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030043 | ||||||
| chr12:53030063
|
AATACAAA others(153): Show |
A | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.979+1879_979+2038d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030063 | |||||
| chr12:53030067
|
C | CAAAAGTT others(151): Show |
2 | a0001c0002t0004g0296a0001c0002t0004g0297 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.979+2025_979+2182d others(160): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030067 | |||||
| chr12:53030067
|
CAAAAGTT others(151): Show |
C | 4 | a0001c0005t0005g0009a0001c0005t0013g0272a0001c0005t0013g0312others(1): Show | 5 | HG02970.hp2 HG06807.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2025_979+2182d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030067 | |||||
| chr12:53030069
|
A | T | 1 | a0001c0001t0002g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.979+1881A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030069 | ||||||
| chr12:53030108
|
G | A | 2 | a0001c0002t0007g0337a0001c0002t0007g0339 | 2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.979+1920G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030108 | ||||||
| chr12:53030162
|
CAGTTAGC others(149): Show |
C | 1 | a0001c0001t0002g0241 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.979+1975_979+2130d others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030162 | ||||||
| chr12:53030225
|
TAA | T | 11 | a0001c0001t0001g0024a0001c0001t0001g0072a0001c0001t0001g0095others(8): Show | 11 | HG01123.hp1 HG03710.hp1 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+2040_979+2041d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030225 | |||||
| chr12:53030227
|
A | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.979+2039A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030227 | ||||||
| chr12:53030330
|
A | G | 1 | a0001c0002t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.979+2142A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030330 | ||||||
| chr12:53030370
|
T | TA | 9 | a0001c0002t0007g0270a0001c0002t0007g0336a0001c0002t0007g0337others(6): Show | 9 | HG01884.hp1 HG02145.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.979+2188dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030370 | |||||
| chr12:53030413
|
C | CT | 10 | a0001c0001t0001g0046a0001c0001t0001g0090a0001c0001t0002g0026others(7): Show | 10 | HG01074.hp1 HG01081.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.979+2250dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0001g0135a0001c0001t0002g0173a0001c0001t0002g0232others(1): Show | 4 | HG01123.hp1 HG02109.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+2241_979+2250d others(12): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0119a0001c0001t0002g0197a0001c0001t0002g0233 | 3 | HG02129.hp2 HG02132.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.979+2240_979+2250d others(13): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0234a0001c0001t0002g0238 | 3 | HG02922.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.979+2239_979+2250d others(14): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0151a0001c0001t0002g0160 | 2 | HG00738.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.979+2237_979+2250d others(16): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0027a0001c0001t0002g0264 | 2 | HG00558.hp1 HG00558.hp2 |
intron_variant | MODIFIER | c.979+2236_979+2250d others(17): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(9): Show |
8 | a0001c0001t0002g0028a0001c0001t0002g0030a0001c0001t0002g0163others(5): Show | 8 | HG02273.hp1 HG02280.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.979+2235_979+2250d others(18): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(10): Show |
9 | a0001c0001t0002g0174a0001c0001t0002g0187a0001c0001t0002g0203others(6): Show | 9 | HG02486.hp2 HG03098.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.979+2234_979+2250d others(19): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(11): Show |
21 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0002g0004others(18): Show | 22 | HG00544.hp1 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.979+2233_979+2250d others(20): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(12): Show |
29 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0087others(26): Show | 30 | HG00140.hp1 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.979+2232_979+2250d others(21): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(13): Show |
19 | a0001c0001t0001g0044a0001c0001t0001g0053a0001c0001t0001g0066others(16): Show | 19 | HG00438.hp2 HG01169.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.979+2231_979+2250d others(22): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(14): Show |
20 | a0001c0001t0001g0020a0001c0001t0001g0051a0001c0001t0001g0057others(17): Show | 20 | HG01123.hp2 HG01167.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.979+2230_979+2250d others(23): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(15): Show |
22 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0040others(19): Show | 22 | HG00280.hp1 HG00280.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.979+2229_979+2250d others(24): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(16): Show |
19 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(16): Show | 20 | HG00140.hp2 HG00735.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.979+2228_979+2250d others(25): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(17): Show |
11 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0060others(8): Show | 11 | HG00642.hp2 HG01952.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.979+2227_979+2250d others(26): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(18): Show |
5 | a0001c0001t0001g0055a0001c0001t0001g0076a0001c0001t0001g0129others(2): Show | 5 | HG01433.hp2 HG02027.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2226_979+2250d others(27): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.979+2250_979+2251i others(28): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(20): Show |
4 | a0001c0001t0001g0041a0001c0001t0001g0049a0001c0001t0001g0084others(1): Show | 4 | HG01978.hp1 NA18991.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.979+2250_979+2251i others(29): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(21): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0039a0001c0001t0001g0073others(1): Show | 4 | HG02165.hp2 NA18978.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+2250_979+2251i others(30): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(22): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0136a0001c0001t0001g0137others(1): Show | 4 | HG01496.hp1 HG01934.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+2250_979+2251i others(31): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0096 | 2 | HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.979+2250_979+2251i others(32): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.979+2250_979+2251i others(33): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0001g0089 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.979+2250_979+2251i others(34): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0138 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.979+2250_979+2251i others(35): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
C | CTTTTTTT others(27): Show |
2 | a0001c0001t0001g0145a0001c0006t0001g0153 | 2 | HG00438.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.979+2250_979+2251i others(36): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
CT | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0106others(13): Show | 17 | HG00609.hp1 HG02027.hp2 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.979+2250delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
CTT | C | 7 | a0001c0001t0001g0097a0001c0001t0001g0148a0001c0001t0001g0256others(4): Show | 7 | HG00423.hp2 HG03486.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.979+2249_979+2250d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
CTTT | C | 41 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0038others(38): Show | 44 | HG00544.hp2 HG00609.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.979+2248_979+2250d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030413
|
CTTTTTTT others(6): Show |
C | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.979+2238_979+2250d others(15): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53030413 | |||||
| chr12:53030482
|
C | T | 5 | a0001c0001t0002g0175a0001c0001t0002g0180a0001c0001t0002g0205others(2): Show | 5 | HG02717.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.979+2294C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030482 | ||||||
| chr12:53030490
|
C | T | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.979+2302C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030490 | ||||||
| chr12:53030683
|
T | A | 2 | a0001c0001t0021g0025a0001c0001t0023g0159 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.979+2495T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030683 | ||||||
| chr12:53030708
|
T | C | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.979+2520T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030708 | ||||||
| chr12:53030859
|
A | C | 1 | a0001c0002t0003g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.979+2671A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030859 | ||||||
| chr12:53030906
|
C | T | 1 | a0001c0002t0004g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.979+2718C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53030906 | ||||||
| chr12:53031019
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.980-2787T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031019 | ||||||
| chr12:53031182
|
TCTC | T | 59 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(56): Show | 61 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.980-2621_980-2619d others(5): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53031182 | |||||
| chr12:53031460
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.980-2346A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031460 | ||||||
| chr12:53031644
|
C | T | 6 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0140others(3): Show | 6 | HG02056.hp2 NA18956.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-2162C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031644 | ||||||
| chr12:53031645
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.980-2161G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031645 | ||||||
| chr12:53031695
|
G | A | 3 | a0001c0005t0013g0272a0001c0005t0013g0312a0001c0005t0013g0334 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.980-2111G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031695 | ||||||
| chr12:53031709
|
G | A | 3 | a0001c0001t0002g0013a0001c0001t0002g0186a0001c0001t0002g0265 | 3 | NA18945.hp2 NA18947.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.980-2097G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031709 | ||||||
| chr12:53031763
|
A | G | 1 | a0001c0001t0002g0164 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.980-2043A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031763 | ||||||
| chr12:53031770
|
G | A | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.980-2036G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031770 | ||||||
| chr12:53031833
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.980-1973G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53031833 | ||||||
| chr12:53032026
|
A | T | 33 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(30): Show | 36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.980-1780A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032026 | ||||||
| chr12:53032052
|
ACTGC | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.980-1747_980-1744d others(6): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53032052 | |||||
| chr12:53032319
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.980-1487A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032319 | ||||||
| chr12:53032386
|
T | G | 1 | a0001c0001t0002g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.980-1420T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032386 | ||||||
| chr12:53032401
|
C | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.980-1405C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032401 | ||||||
| chr12:53032493
|
C | T | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.980-1313C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032493 | ||||||
| chr12:53032669
|
G | GT | 126 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0001g0059others(123): Show | 128 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.980-1122dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53032669 | |||||
| chr12:53032669
|
G | GTT | 8 | a0001c0001t0002g0026a0001c0001t0002g0160a0001c0001t0002g0179others(5): Show | 8 | HG00544.hp1 HG01891.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.980-1123_980-1122d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53032669 | |||||
| chr12:53032669
|
G | T | 3 | a0001c0001t0002g0163a0001c0001t0002g0174a0001c0001t0002g0201 | 3 | NA18998.hp1 NA19004.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.980-1137G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032669 | ||||||
| chr12:53032670
|
T | G | 1 | a0001c0002t0003g0315 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.980-1136T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032670 | ||||||
| chr12:53032724
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.980-1082G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032724 | ||||||
| chr12:53032782
|
C | A | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(259): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.980-1024C>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032782 | ||||||
| chr12:53032901
|
T | C | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(293): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.980-905T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032901 | ||||||
| chr12:53032963
|
G | A | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.980-843G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53032963 | ||||||
| chr12:53033007
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.980-799A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033007 | ||||||
| chr12:53033011
|
A | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(261): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.980-795A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033011 | ||||||
| chr12:53033164
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.980-642C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033164 | ||||||
| chr12:53033334
|
C | CT | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(283): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.980-460dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53033334 | |||||
| chr12:53033334
|
C | CTT | 8 | a0001c0001t0001g0077a0001c0001t0001g0110a0001c0001t0001g0126others(5): Show | 8 | HG01496.hp1 NA18945.hp1 NA19000.hp2 others(5): Show |
intron_variant | MODIFIER | c.980-461_980-460dup others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr12 | 53033334 | |||||
| chr12:53033366
|
C | T | 1 | a0001c0002t0004g0295 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.980-440C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033366 | ||||||
| chr12:53033398
|
AG | A | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.980-407delG | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033398 | ||||||
| chr12:53033447
|
A | G | 1 | a0001c0001t0014g0014 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.980-359A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033447 | ||||||
| chr12:53033543
|
A | G | 1 | a0001c0002t0005g0333 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.980-263A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033543 | ||||||
| chr12:53033650
|
T | C | 2 | a0001c0002t0003g0305a0001c0002t0003g0308 | 2 | HG02056.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.980-156T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 8/14 | chr12 | 53033650 | ||||||
| chr12:53034042
|
G | T | 5 | a0001c0002t0003g0271a0001c0002t0003g0305a0001c0002t0003g0306others(2): Show | 5 | HG02056.hp1 NA18940.hp1 NA18975.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1208+8G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 9/14 | chr12 | 53034042 | ||||||
| chr12:53034870
|
G | A | 1 | a0001c0001t0006g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1306+161G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53034870 | ||||||
| chr12:53034886
|
A | C | 2 | a0001c0002t0004g0296a0001c0002t0004g0297 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1306+177A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53034886 | ||||||
| chr12:53034956
|
C | CT | 11 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0086others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306+269dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | |||||
| chr12:53034956
|
C | CTT | 33 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(30): Show | 36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1306+268_1306+269d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | |||||
| chr12:53034956
|
CT | C | 117 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(114): Show | 119 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.1306+269delT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | |||||
| chr12:53034956
|
CTT | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1306+268_1306+269d others(4): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53034956 | |||||
| chr12:53035017
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1306+308T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035017 | ||||||
| chr12:53035287
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1306+578C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035287 | ||||||
| chr12:53035347
|
C | G | 1 | a0001c0002t0007g0339 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1306+638C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035347 | ||||||
| chr12:53035371
|
A | AT | 4 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0002g0215others(1): Show | 4 | HG02647.hp1 HG02970.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+666dupT | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53035371 | |||||
| chr12:53035371
|
A | T | 8 | a0001c0001t0002g0160a0001c0001t0002g0164a0001c0001t0008g0035others(5): Show | 8 | HG01891.hp2 HG02630.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306+662A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035371 | ||||||
| chr12:53035375
|
T | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(127): Show | 132 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.1306+666T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035375 | ||||||
| chr12:53035376
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1306+667C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035376 | ||||||
| chr12:53035379
|
T | A | 3 | a0001c0001t0006g0016a0001c0001t0006g0032a0001c0001t0006g0037 | 3 | HG01070.hp2 HG03017.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1306+670T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035379 | ||||||
| chr12:53035432
|
G | A | 1 | a0001c0001t0006g0016 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1306+723G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035432 | ||||||
| chr12:53035495
|
A | C | 5 | a0001c0002t0003g0271a0001c0002t0003g0305a0001c0002t0003g0306others(2): Show | 5 | HG02056.hp1 NA18940.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+786A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035495 | ||||||
| chr12:53035526
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1306+817A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035526 | ||||||
| chr12:53035663
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1306+954C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035663 | ||||||
| chr12:53035812
|
C | G | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1306+1103C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53035812 | ||||||
| chr12:53035987
|
T | TTTTGTAT others(18): Show |
98 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(95): Show | 104 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1306+1282_1306+128 others(29): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53035987 | |||||
| chr12:53035987
|
T | TTTTGTAT others(18): Show |
263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1306+1282_1306+128 others(29): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53035987 | |||||
| chr12:53036068
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1307-1341G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036068 | ||||||
| chr12:53036082
|
CCTT | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1307-1324_1307-132 others(7): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 53036082 | |||||
| chr12:53036135
|
G | A | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1307-1274G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036135 | ||||||
| chr12:53036221
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1307-1188T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036221 | ||||||
| chr12:53036230
|
A | G | 2 | a0001c0002t0015g0281a0003c0009t0015g0304 | 2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1307-1179A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036230 | ||||||
| chr12:53036319
|
G | A | 1 | a0001c0001t0002g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1307-1090G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036319 | ||||||
| chr12:53036408
|
G | A | 1 | a0001c0002t0009g0318 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1307-1001G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036408 | ||||||
| chr12:53036469
|
C | T | 1 | a0001c0002t0003g0311 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1307-940C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036469 | ||||||
| chr12:53036561
|
A | G | 1 | a0001c0002t0003g0310 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1307-848A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036561 | ||||||
| chr12:53036649
|
A | T | 110 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0013others(107): Show | 112 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1307-760A>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036649 | ||||||
| chr12:53036653
|
A | G | 1 | a0001c0001t0006g0036 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1307-756A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036653 | ||||||
| chr12:53036725
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(64): Show | 69 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1307-684C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036725 | ||||||
| chr12:53036840
|
C | T | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1307-569C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036840 | ||||||
| chr12:53036993
|
G | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1307-416G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53036993 | ||||||
| chr12:53037025
|
A | G | 1 | a0001c0001t0002g0173 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1307-384A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53037025 | ||||||
| chr12:53037083
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(330): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1307-326T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53037083 | ||||||
| chr12:53037226
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(261): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1307-183T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 10/14 | chr12 | 53037226 | ||||||
| chr12:53037749
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0072a0001c0001t0001g0073others(5): Show | 8 | HG02040.hp1 NA18948.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.1520+127C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037749 | ||||||
| chr12:53037924
|
C | G | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1520+302C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037924 | ||||||
| chr12:53037960
|
A | G | 8 | a0001c0001t0002g0004a0001c0001t0002g0189a0001c0001t0002g0192others(5): Show | 9 | HG00642.hp1 HG00738.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1520+338A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037960 | ||||||
| chr12:53037975
|
T | C | 1 | a0002c0004t0010g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1520+353T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037975 | ||||||
| chr12:53037984
|
G | A | 2 | a0001c0002t0003g0006a0001c0002t0003g0007 | 4 | NA18944.hp2 NA18956.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1520+362G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53037984 | ||||||
| chr12:53038053
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1521-303C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038053 | ||||||
| chr12:53038100
|
G | A | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1521-256G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038100 | ||||||
| chr12:53038150
|
T | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0256 | 3 | NA18990.hp1 NA19009.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1521-206T>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038150 | ||||||
| chr12:53038292
|
T | G | 33 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(30): Show | 36 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.1521-64T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038292 | ||||||
| chr12:53038304
|
T | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1521-52T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038304 | ||||||
| chr12:53038323
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0022others(52): Show | 56 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1521-33A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 11/14 | chr12 | 53038323 | ||||||
| chr12:53038491
|
A | G | 1 | a0001c0001t0002g0013 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1576+80A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038491 | ||||||
| chr12:53038513
|
G | A | 32 | a0001c0002t0003g0006a0001c0002t0003g0007a0001c0002t0003g0010others(29): Show | 35 | HG00423.hp2 HG00544.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.1576+102G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038513 | ||||||
| chr12:53038707
|
C | T | 33 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0275others(30): Show | 34 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1576+296C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038707 | ||||||
| chr12:53038749
|
G | A | 14 | a0001c0001t0002g0004a0001c0001t0002g0161a0001c0001t0002g0165others(11): Show | 15 | HG00544.hp1 HG00642.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1576+338G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53038749 | ||||||
| chr12:53038816
|
C | CA | 25 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0276others(22): Show | 26 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1577-412dupA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 53038816 | |||||
| chr12:53038816
|
CA | C | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1577-412delA | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr12 | 53038816 | |||||
| chr12:53039152
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(261): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1577-86A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039152 | ||||||
| chr12:53039169
|
G | C | 1 | a0001c0001t0002g0264 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1577-69G>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039169 | ||||||
| chr12:53039176
|
T | G | 1 | a0001c0001t0002g0223 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1577-62T>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039176 | ||||||
| chr12:53039194
|
T | C | 21 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0172others(18): Show | 21 | HG01106.hp2 HG02015.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1577-44T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 12/14 | chr12 | 53039194 | ||||||
| chr12:53039381
|
CAT | C | 7 | a0001c0002t0003g0271a0001c0002t0003g0305a0001c0002t0003g0306others(4): Show | 7 | HG02055.hp2 HG02056.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1682+39_1682+40del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039381 | ||||||
| chr12:53039515
|
A | C | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1683-115A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039515 | ||||||
| chr12:53039553
|
G | T | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1683-77G>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039553 | ||||||
| chr12:53039557
|
C | T | 1 | a0001c0002t0015g0281 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1683-73C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039557 | ||||||
| chr12:53039570
|
CAT | C | 3 | a0001c0005t0013g0272a0001c0005t0013g0312a0001c0005t0013g0334 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1683-59_1683-58del others(2): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039570 | ||||||
| chr12:53039619
|
C | T | 3 | a0001c0001t0008g0031a0001c0001t0008g0035a0001c0001t0008g0199 | 3 | NA18944.hp1 NA18978.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1683-11C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 13/14 | chr12 | 53039619 | ||||||
| chr12:53039746
|
T | C | 1 | a0001c0002t0003g0362 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1755+44T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039746 | ||||||
| chr12:53039804
|
T | C | 1 | a0001c0005t0005g0009 | 2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1755+102T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039804 | ||||||
| chr12:53039809
|
G | A | 1 | a0001c0002t0020g0342 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1755+107G>A | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039809 | ||||||
| chr12:53039861
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1755+159C>T | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039861 | ||||||
| chr12:53039865
|
A | AT | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(297): Show | 307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1755+163_1755+164i others(3): Show |
EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039865 | ||||||
| chr12:53039893
|
T | C | 3 | a0001c0002t0011g0359a0001c0002t0011g0360a0001c0002t0011g0361 | 3 | HG01891.hp1 HG02572.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1755+191T>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039893 | ||||||
| chr12:53039925
|
C | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1756-218C>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039925 | ||||||
| chr12:53039969
|
A | G | 25 | a0001c0002t0004g0005a0001c0002t0004g0274a0001c0002t0004g0276others(22): Show | 26 | HG00423.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1756-174A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53039969 | ||||||
| chr12:53040004
|
A | G | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0011others(260): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1756-139A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53040004 | ||||||
| chr12:53040011
|
A | G | 1 | a0001c0001t0006g0032 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1756-132A>G | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53040011 | ||||||
| chr12:53040070
|
A | C | 1 | a0001c0001t0002g0216 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1756-73A>C | EIF4B | ENSG00000063046.18 | transcript | ENST00000262056.14 | protein_coding | 14/14 | chr12 | 53040070 |