Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 56478 |
|---|---|
| ensemblid | ENSG00000184708.18 |
| hgncid | 16687 |
| symbol | EIF4ENIF1 |
| name | eukaryotic translation initiation factor 4E nuclear import factor 1 |
| refseq_nuc | NM_019843.4 |
| refseq_prot | NP_062817.2 |
| ensembl_nuc | ENST00000330125.10 |
| ensembl_prot | ENSP00000328103.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 31439367 |
| end | 31489842 |
| strand | - |
| ver | v1.2 |
| region | chr22:31439367-31489842 |
| region5000 | chr22:31434367-31494842 |
| regionname0 | EIF4ENIF1_chr22_31439367_31489842 |
| regionname5000 | EIF4ENIF1_chr22_31434367_31494842 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 985 | 361 | 78 | 70 | 160 | 14 | 37 | 129 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0002 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0003 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0004 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0005 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0006 | 0/0 | 985 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2958 | 212 | 39 | 54 | 98 | 9 | 11 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0002 | 0/1 | 2958 | 68 | 2 | 2 | 53 | 1 | 9 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0003 | 0/0 | 2958 | 60 | 24 | 14 | 3 | 4 | 15 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0004 | 0/0 | 2958 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0005 | 0/0 | 2958 | 4 | 4 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0006 | 0/0 | 2958 | 4 | 0 | 0 | 4 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0007 | 0/0 | 2958 | 2 | 1 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0008 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0009 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0010 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0011 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0012 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0013 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0014 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| c0015 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 690 | 342 | 76 | 65 | 150 | 11 | 38 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| t0002 | 0/0 | 690 | 18 | 3 | 3 | 12 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| t0003 | 0/0 | 690 | 3 | 0 | 1 | 0 | 2 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| t0004 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| t0005 | 0/0 | 690 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| t0006 | 0/0 | 690 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2958 | 212 | 39 | 54 | 98 | 9 | 11 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0002 | 0/1 | 2958 | 68 | 2 | 2 | 53 | 1 | 9 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0003 | 0/0 | 2958 | 60 | 24 | 14 | 3 | 4 | 15 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0004 | 0/0 | 2958 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0005 | 0/0 | 2958 | 4 | 4 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0006 | 0/0 | 2958 | 4 | 0 | 0 | 4 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0007 | 0/0 | 2958 | 2 | 1 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0010 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0013 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0014 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0002c0015 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0003c0011 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0004c0009 | 0/0 | 2958 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0005c0012 | 0/0 | 2958 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0006c0008 | 0/0 | 2958 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3647 | 190 | 36 | 50 | 86 | 6 | 11 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0001t0002 | 0/0 | 3647 | 18 | 3 | 3 | 12 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0001t0003 | 0/0 | 3647 | 3 | 0 | 1 | 0 | 2 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0001t0005 | 0/0 | 3647 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0002t0001 | 0/1 | 3647 | 68 | 2 | 2 | 53 | 1 | 9 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0003t0001 | 0/0 | 3647 | 58 | 23 | 13 | 3 | 4 | 15 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0003t0004 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0003t0006 | 0/0 | 3647 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0004t0001 | 0/0 | 3647 | 8 | 8 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0005t0001 | 0/0 | 3647 | 4 | 4 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0006t0001 | 0/0 | 3647 | 4 | 0 | 0 | 4 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0007t0001 | 0/0 | 3647 | 2 | 1 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0010t0001 | 0/0 | 3647 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0013t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0001c0014t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0002c0015t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0003c0011t0001 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0004c0009t0001 | 0/0 | 3647 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0005c0012t0001 | 0/0 | 3647 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| a0006c0008t0001 | 0/0 | 3647 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | copy fasta | chr22 | 31434367 | 31494842 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0003t0006g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0007t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0007t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0010t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0013t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0001c0014t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0002c0015t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0003c0011t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0004c0009t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0005c0012t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| a0006c0008t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0235 | EUR | GBR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00140 | hp2 | a0001 | c0003 | t0001 | g0291 | EUR | GBR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0238 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0295 | EUR | FIN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0052 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | CHS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0290 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0341 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0331 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0320 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0322 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0285 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0342 | AMR | PUR | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0139 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0288 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01358 | hp2 | a0001 | c0003 | t0006 | g0364 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0289 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0293 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0294 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0362 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0299 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0313 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02027 | hp1 | a0002 | c0015 | t0001 | g0357 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0318 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0333 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | PEL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02572 | hp1 | a0004 | c0009 | t0001 | g0146 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0335 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02602 | hp2 | a0001 | c0003 | t0001 | g0319 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0337 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0347 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0113 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0148 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0287 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0351 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0350 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02738 | hp1 | a0001 | c0003 | t0001 | g0324 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0144 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0110 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0276 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02895 | hp2 | a0001 | c0003 | t0001 | g0328 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0326 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02965 | hp2 | a0001 | c0007 | t0001 | g0363 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03130 | hp2 | a0003 | c0011 | t0001 | g0263 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0334 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0253 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0211 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0339 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0062 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0020 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0302 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0269 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0352 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0115 | AFR | ESN | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0147 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0349 | AFR | GWD | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0323 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0338 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0321 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0343 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0332 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03831 | hp2 | a0006 | c0008 | t0001 | g0098 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03834 | hp1 | a0001 | c0003 | t0001 | g0354 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0356 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03927 | hp2 | a0001 | c0010 | t0001 | g0078 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0292 | SAS | BEB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0325 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG04204 | hp2 | a0001 | c0007 | t0001 | g0108 | SAS | STU | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18522 | hp1 | a0001 | c0004 | t0001 | g0111 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0300 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CHB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | CHB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18949 | hp1 | a0001 | c0006 | t0001 | g0203 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18954 | hp2 | a0001 | c0014 | t0001 | g0116 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18972 | hp1 | a0001 | c0003 | t0001 | g0346 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18988 | hp1 | a0001 | c0006 | t0001 | g0229 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18992 | hp1 | a0001 | c0006 | t0001 | g0142 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18995 | hp2 | a0005 | c0012 | t0001 | g0035 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19002 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0296 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19057 | hp2 | a0001 | c0006 | t0001 | g0176 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19084 | hp1 | a0001 | c0013 | t0001 | g0163 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19240 | hp1 | a0001 | c0004 | t0001 | g0114 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0303 | AFR | YRI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ASW | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ASW | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0330 | EUR | TSI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0241 | EUR | TSI | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0112 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0327 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0345 | AFR | ACB | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0107 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0311 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | USA | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| NA21309 | hp2 | a0001 | c0003 | t0001 | g0301 | AFR | LWK | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0029 | REF | REF | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0119 | REF | REF | EIF4ENIF1_chr22_31434367_31494842 | EIF4ENIF1 | chr22 | 31434367 | 31494842 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31441992
|
G | A | 1 | a0005 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.2333C>T | p.Thr778Ile | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/19 | 2509/3647 | 2333/2958 | 778/985 | chr22 | 31441992 | ||
| chr22:31447561
|
C | T | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1853G>A | p.Ser618Asn | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/19 | 2029/3647 | 1853/2958 | 618/985 | chr22 | 31447561 | ||
| chr22:31454251
|
C | T | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1405G>A | p.Val469Ile | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/19 | 1581/3647 | 1405/2958 | 469/985 | chr22 | 31454251 | ||
| chr22:31471917
|
C | T | 1 | a0006 | 1 | HG03831.hp2 | missense_variant&splice_region_variant | MODERATE | c.97G>A | p.Glu33Lys | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/19 | 273/3647 | 97/2958 | 33/985 | chr22 | 31471917 | ||
| chr22:31488654
|
G | A | 1 | a0002 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.65C>T | p.Pro22Leu | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/19 | 241/3647 | 65/2958 | 22/985 | chr22 | 31488654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31440813
|
G | A | 1 | a0001c0007 | 2 | HG02965.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.2607C>T | p.Ile869Ile | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/19 | 2783/3647 | 2607/2958 | 869/985 | chr22 | 31440813 | ||
| chr22:31442099
|
G | A | 2 | a0001c0003a0002c0015 | 61 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(58): Show |
synonymous_variant | LOW | c.2226C>T | p.Ser742Ser | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/19 | 2402/3647 | 2226/2958 | 742/985 | chr22 | 31442099 | ||
| chr22:31447503
|
A | C | 1 | a0001c0006 | 4 | NA18949.hp1 NA18988.hp1 NA18992.hp1 others(1): Show |
synonymous_variant | LOW | c.1911T>G | p.Ala637Ala | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/19 | 2087/3647 | 1911/2958 | 637/985 | chr22 | 31447503 | ||
| chr22:31454252
|
G | A | 1 | a0001c0004 | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
synonymous_variant | LOW | c.1404C>T | p.Ala468Ala | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/19 | 1580/3647 | 1404/2958 | 468/985 | chr22 | 31454252 | ||
| chr22:31455260
|
A | C | 2 | a0001c0005a0004c0009 | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
synonymous_variant | LOW | c.1155T>G | p.Pro385Pro | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/19 | 1331/3647 | 1155/2958 | 385/985 | chr22 | 31455260 | ||
| chr22:31463798
|
G | T | 3 | a0001c0005a0001c0010a0004c0009 | 6 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
synonymous_variant | LOW | c.468C>A | p.Gly156Gly | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/19 | 644/3647 | 468/2958 | 156/985 | chr22 | 31463798 | ||
| chr22:31463873
|
A | G | 2 | a0001c0002a0001c0014 | 69 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
synonymous_variant | LOW | c.393T>C | p.Val131Val | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/19 | 569/3647 | 393/2958 | 131/985 | chr22 | 31463873 | ||
| chr22:31463894
|
G | A | 1 | a0001c0013 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.372C>T | p.Gly124Gly | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/19 | 548/3647 | 372/2958 | 124/985 | chr22 | 31463894 | ||
| chr22:31488647
|
G | C | 1 | a0001c0014 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.72C>G | p.Ser24Ser | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/19 | 248/3647 | 72/2958 | 24/985 | chr22 | 31488647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31439520
|
T | C | 1 | a0001c0003t0004 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 360 | chr22 | 31439520 | |||||
| chr22:31439692
|
T | G | 1 | a0001c0001t0005 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 188 | chr22 | 31439692 | |||||
| chr22:31439732
|
T | C | 1 | a0001c0001t0003 | 3 | HG00140.hp1 HG00639.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*148A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 148 | chr22 | 31439732 | |||||
| chr22:31439745
|
A | G | 1 | a0001c0001t0002 | 18 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*135T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 19/19 | 135 | chr22 | 31439745 | |||||
| chr22:31489708
|
G | A | 1 | a0001c0003t0006 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/19 | 990 | chr22 | 31489708 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:31440265
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2717-144T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440265 | ||||||
| chr22:31440392
|
G | T | 343 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2717-271C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440392 | ||||||
| chr22:31440460
|
C | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2716+244G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440460 | ||||||
| chr22:31440500
|
T | C | 124 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(121): Show | 124 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2716+204A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440500 | ||||||
| chr22:31440612
|
A | C | 1 | a0001c0001t0001g0154 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2716+92T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 18/18 | chr22 | 31440612 | ||||||
| chr22:31441147
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0175 | 2 | HG02132.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2552-279G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441147 | ||||||
| chr22:31441148
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2552-280C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441148 | ||||||
| chr22:31441208
|
G | A | 1 | a0001c0002t0001g0079 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2552-340C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441208 | ||||||
| chr22:31441240
|
G | A | 2 | a0001c0002t0001g0068a0001c0002t0001g0086 | 2 | HG02056.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.2552-372C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441240 | ||||||
| chr22:31441294
|
T | C | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2552-426A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441294 | ||||||
| chr22:31441341
|
C | T | 13 | a0001c0001t0001g0088a0001c0001t0001g0090a0001c0001t0001g0092others(10): Show | 13 | HG01123.hp1 HG01243.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.2551+433G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441341 | ||||||
| chr22:31441406
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2551+368C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441406 | ||||||
| chr22:31441467
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2551+307C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441467 | ||||||
| chr22:31441473
|
G | C | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2551+301C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441473 | ||||||
| chr22:31441514
|
A | T | 3 | a0001c0002t0001g0033a0001c0002t0001g0049a0001c0002t0001g0061 | 3 | HG00544.hp1 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2551+260T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441514 | ||||||
| chr22:31441550
|
G | GA | 98 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(95): Show | 99 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.2551+223dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAA | 12 | a0001c0001t0001g0210a0001c0001t0001g0304a0001c0001t0001g0317others(9): Show | 12 | HG02083.hp1 HG02145.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.2551+222_2551+223d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAA | 8 | a0001c0001t0002g0266a0001c0001t0002g0267a0001c0001t0002g0272others(5): Show | 8 | HG00408.hp2 HG01934.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.2551+219_2551+223d others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAAA | 6 | a0001c0001t0002g0265a0001c0001t0002g0268a0001c0001t0002g0274others(3): Show | 6 | HG00609.hp1 HG01346.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.2551+218_2551+223d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAAAA others(6): Show |
1 | a0001c0001t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2551+211_2551+223d others(15): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAAAA others(13): Show |
1 | a0001c0001t0002g0281 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2551+204_2551+223d others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAAAA others(14): Show |
1 | a0001c0001t0002g0271 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2551+203_2551+223d others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAAAA others(15): Show |
1 | a0001c0001t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2551+202_2551+223d others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAAAA others(17): Show |
1 | a0001c0001t0002g0270 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2551+223_2551+224i others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
G | GAAAAAAA others(23): Show |
1 | a0001c0001t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2551+223_2551+224i others(32): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441550
|
GA | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0209a0001c0001t0001g0213others(9): Show | 12 | HG00323.hp1 HG02109.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2551+223delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441550 | ||||||
| chr22:31441551
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2551+223T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441551 | ||||||
| chr22:31441572
|
AAG | A | 8 | a0001c0003t0001g0311a0001c0003t0001g0326a0001c0003t0001g0328others(5): Show | 8 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2551+200_2551+201d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 17/18 | chr22 | 31441572 | ||||||
| chr22:31442265
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2207-147G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442265 | ||||||
| chr22:31442480
|
T | C | 1 | a0001c0002t0001g0015 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2207-362A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442480 | ||||||
| chr22:31442483
|
G | A | 23 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(20): Show | 23 | HG00408.hp2 HG00609.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.2207-365C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442483 | ||||||
| chr22:31442532
|
C | T | 122 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(119): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.2207-414G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442532 | ||||||
| chr22:31442597
|
T | G | 1 | a0001c0005t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2206+365A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442597 | ||||||
| chr22:31442695
|
A | T | 1 | a0001c0002t0001g0080 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2206+267T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442695 | ||||||
| chr22:31442778
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2206+184A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442778 | ||||||
| chr22:31442831
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2206+131C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442831 | ||||||
| chr22:31442896
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2206+66G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 16/18 | chr22 | 31442896 | ||||||
| chr22:31443165
|
T | C | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2074-71A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443165 | ||||||
| chr22:31443205
|
T | C | 1 | a0001c0007t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2074-111A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443205 | ||||||
| chr22:31443258
|
G | A | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2074-164C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443258 | ||||||
| chr22:31443314
|
G | A | 1 | a0001c0003t0001g0276 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2074-220C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443314 | ||||||
| chr22:31443419
|
T | TCTGCAAA others(2): Show |
24 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(21): Show | 24 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.2074-326_2074-325i others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443419 | ||||||
| chr22:31443419
|
T | TCTGCGAA others(2): Show |
319 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.2074-326_2074-325i others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443419 | ||||||
| chr22:31443474
|
C | T | 2 | a0001c0007t0001g0108a0001c0007t0001g0363 | 2 | HG02965.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2074-380G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443474 | ||||||
| chr22:31443654
|
T | C | 8 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0209others(5): Show | 8 | HG02148.hp1 NA18947.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2074-560A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443654 | ||||||
| chr22:31443742
|
AT | A | 7 | a0001c0001t0001g0133a0001c0001t0002g0279a0001c0005t0001g0144others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2074-649delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443742 | ||||||
| chr22:31443806
|
C | CT | 185 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(182): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.2074-713dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443806 | ||||||
| chr22:31443806
|
CT | C | 10 | a0001c0001t0001g0056a0001c0001t0002g0274a0001c0004t0001g0107others(7): Show | 10 | HG00609.hp1 HG02109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2074-713delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443806 | ||||||
| chr22:31443964
|
T | C | 79 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0050others(76): Show | 79 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.2073+642A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31443964 | ||||||
| chr22:31444049
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2073+557G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444049 | ||||||
| chr22:31444109
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0210 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2073+497A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444109 | ||||||
| chr22:31444393
|
A | G | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2073+213T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444393 | ||||||
| chr22:31444488
|
G | C | 21 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(18): Show | 21 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.2073+118C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 15/18 | chr22 | 31444488 | ||||||
| chr22:31444707
|
TATC | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1989-20_1989-18del others(3): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31444707 | ||||||
| chr22:31444762
|
A | C | 1 | a0001c0002t0001g0015 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1989-72T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31444762 | ||||||
| chr22:31444834
|
T | C | 24 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(21): Show | 24 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.1989-144A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31444834 | ||||||
| chr22:31445054
|
T | C | 28 | a0001c0001t0001g0063a0001c0001t0001g0141a0001c0001t0001g0154others(25): Show | 28 | HG00408.hp1 HG00423.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1989-364A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445054 | ||||||
| chr22:31445063
|
A | T | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1989-373T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445063 | ||||||
| chr22:31445105
|
A | G | 69 | a0001c0001t0001g0284a0001c0002t0001g0001a0001c0002t0001g0003others(66): Show | 70 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1989-415T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445105 | ||||||
| chr22:31445301
|
GAATC | G | 117 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1989-615_1989-612d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445301 | ||||||
| chr22:31445763
|
T | A | 153 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1989-1073A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445763 | ||||||
| chr22:31445839
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1989-1149A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445839 | ||||||
| chr22:31445953
|
G | GC | 81 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.1989-1264dupG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445953 | ||||||
| chr22:31445953
|
G | GCC | 41 | a0001c0001t0001g0118a0001c0001t0001g0138a0001c0001t0001g0169others(38): Show | 41 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.1989-1265_1989-126 others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445953 | ||||||
| chr22:31445953
|
G | GCCC | 49 | a0001c0001t0001g0284a0001c0001t0002g0266a0001c0001t0002g0268others(46): Show | 50 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1989-1266_1989-126 others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445953 | ||||||
| chr22:31445963
|
C | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0137 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1989-1273G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31445963 | ||||||
| chr22:31446027
|
T | G | 6 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1989-1337A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446027 | ||||||
| chr22:31446104
|
C | T | 63 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0050others(60): Show | 63 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.1988+1322G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446104 | ||||||
| chr22:31446137
|
T | A | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1988+1289A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446137 | ||||||
| chr22:31446144
|
G | C | 1 | a0001c0014t0001g0116 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1988+1282C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446144 | ||||||
| chr22:31446174
|
A | C | 1 | a0001c0002t0001g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1988+1252T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446174 | ||||||
| chr22:31446192
|
T | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1988+1234A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446192 | ||||||
| chr22:31446251
|
C | T | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1988+1175G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446251 | ||||||
| chr22:31446285
|
C | CAAAAAA | 6 | a0001c0001t0001g0125a0001c0001t0001g0135a0001c0001t0001g0205others(3): Show | 6 | HG00323.hp1 HG01070.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1988+1135_1988+114 others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | ||||||
| chr22:31446285
|
C | CAAAAAAA | 222 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0024others(219): Show | 223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1988+1134_1988+114 others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | ||||||
| chr22:31446285
|
C | CAAAAAAA others(1): Show |
55 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 55 | HG00408.hp2 HG00609.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1988+1133_1988+114 others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | ||||||
| chr22:31446285
|
C | CAAAAAAA others(2): Show |
58 | a0001c0001t0001g0008a0001c0001t0001g0264a0001c0002t0001g0001others(55): Show | 59 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1988+1132_1988+114 others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | ||||||
| chr22:31446285
|
C | CAAAAAAA others(3): Show |
5 | a0001c0002t0001g0022a0001c0002t0001g0045a0001c0002t0001g0081others(2): Show | 5 | HG02083.hp1 HG03710.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1988+1131_1988+114 others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | ||||||
| chr22:31446285
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0001g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1988+1130_1988+114 others(15): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446285 | ||||||
| chr22:31446417
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1988+1009C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446417 | ||||||
| chr22:31446568
|
C | T | 116 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1988+858G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31446568 | ||||||
| chr22:31447060
|
G | A | 1 | a0001c0002t0001g0058 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1988+366C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31447060 | ||||||
| chr22:31447392
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1988+34C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 14/18 | chr22 | 31447392 | ||||||
| chr22:31447581
|
G | C | 116 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1849-16C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 13/18 | chr22 | 31447581 | ||||||
| chr22:31447947
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+206T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 13/18 | chr22 | 31447947 | ||||||
| chr22:31448237
|
C | T | 2 | a0001c0003t0001g0020a0001c0003t0001g0319 | 2 | HG02602.hp2 HG03239.hp2 |
splice_region_variant&intron_variant | LOW | c.1769-5G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448237 | ||||||
| chr22:31448256
|
G | A | 1 | a0001c0003t0001g0303 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1769-24C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448256 | ||||||
| chr22:31448284
|
G | A | 4 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0029others(1): Show | 5 | HG00280.hp2 HG01106.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1769-52C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448284 | ||||||
| chr22:31448307
|
A | C | 316 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(313): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1769-75T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448307 | ||||||
| chr22:31448387
|
A | C | 79 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0050others(76): Show | 79 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1769-155T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448387 | ||||||
| chr22:31448776
|
T | A | 1 | a0001c0001t0001g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1769-544A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448776 | ||||||
| chr22:31448838
|
A | G | 2 | a0001c0002t0001g0080a0001c0002t0001g0081 | 2 | HG03704.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1768+510T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448838 | ||||||
| chr22:31448860
|
CT | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1768+487delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31448860 | ||||||
| chr22:31449158
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1768+190C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31449158 | ||||||
| chr22:31449163
|
A | G | 116 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1768+185T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31449163 | ||||||
| chr22:31449167
|
C | T | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1768+181G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 12/18 | chr22 | 31449167 | ||||||
| chr22:31449734
|
C | CT | 87 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(84): Show | 88 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.1585-204dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449734 | ||||||
| chr22:31449756
|
A | T | 1 | a0001c0002t0001g0191 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1585-225T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449756 | ||||||
| chr22:31449815
|
C | T | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585-284G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449815 | ||||||
| chr22:31449834
|
G | A | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1585-303C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31449834 | ||||||
| chr22:31450093
|
C | CT | 78 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0055others(75): Show | 78 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.1584+195dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31450093 | ||||||
| chr22:31450120
|
C | T | 1 | a0001c0003t0001g0346 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1584+169G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 11/18 | chr22 | 31450120 | ||||||
| chr22:31450463
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1513-103A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450463 | ||||||
| chr22:31450469
|
A | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01243.hp1 HG02559.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1513-109T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450469 | ||||||
| chr22:31450719
|
G | GAC | 3 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1513-361_1513-360d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450719 | ||||||
| chr22:31450719
|
GAC | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 211 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1513-361_1513-360d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450719 | ||||||
| chr22:31450719
|
GACAC | G | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1513-363_1513-360d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450719 | ||||||
| chr22:31450723
|
C | G | 2 | a0001c0003t0001g0124a0001c0003t0001g0294 | 2 | HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1513-363G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450723 | ||||||
| chr22:31450740
|
A | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0152 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1513-380T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450740 | ||||||
| chr22:31450740
|
ACT | A | 116 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1513-382_1513-381d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450740 | ||||||
| chr22:31450753
|
CACATACA others(5): Show |
C | 1 | a0001c0003t0001g0337 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1513-405_1513-394d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450753 | ||||||
| chr22:31450757
|
TACATATA others(19): Show |
T | 1 | a0001c0002t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1513-423_1513-398d others(28): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450757 | ||||||
| chr22:31450763
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1513-403A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450763 | ||||||
| chr22:31450797
|
TACATAC | T | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361 | 3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1513-443_1513-438d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450797 | ||||||
| chr22:31450801
|
TACACATA others(7): Show |
T | 3 | a0001c0001t0001g0247a0001c0001t0001g0256a0001c0007t0001g0108 | 3 | HG01934.hp2 HG02293.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1513-455_1513-442d others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450801 | ||||||
| chr22:31450831
|
CAT | C | 79 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0050others(76): Show | 79 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(76): Show |
intron_variant | MODIFIER | c.1513-473_1513-472d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450831 | ||||||
| chr22:31450833
|
T | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1513-473A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450833 | ||||||
| chr22:31450842
|
AC | A | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1513-483delG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450842 | ||||||
| chr22:31450844
|
T | TAC | 51 | a0001c0001t0001g0008a0001c0001t0001g0094a0001c0001t0001g0102others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.1513-486_1513-485d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
T | TACAC | 37 | a0001c0001t0001g0002a0001c0001t0001g0063a0001c0001t0001g0089others(34): Show | 38 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1513-488_1513-485d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
T | TACACAC | 21 | a0001c0001t0001g0030a0001c0001t0001g0087a0001c0001t0001g0090others(18): Show | 21 | HG00423.hp1 HG00741.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.1513-490_1513-485d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
T | TACACACA others(1): Show |
36 | a0001c0001t0001g0006a0001c0001t0001g0050a0001c0001t0001g0091others(33): Show | 36 | HG00423.hp2 HG00735.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1513-492_1513-485d others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
T | TACACACA others(3): Show |
17 | a0001c0001t0001g0024a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 17 | HG00140.hp1 HG00323.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1513-494_1513-485d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
T | TACACACA others(5): Show |
4 | a0001c0001t0001g0106a0001c0001t0001g0141a0001c0001t0001g0197others(1): Show | 4 | HG01169.hp2 HG01978.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1513-496_1513-485d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1513-498_1513-485d others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
T | TACACACA others(9): Show |
3 | a0001c0001t0001g0172a0001c0001t0001g0226a0001c0001t0002g0265 | 3 | NA18949.hp2 NA18955.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1513-500_1513-485d others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TAC | T | 25 | a0001c0001t0001g0071a0001c0001t0001g0140a0001c0001t0001g0314others(22): Show | 25 | HG00544.hp1 HG01081.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1513-486_1513-485d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACAC | T | 23 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0125others(20): Show | 23 | HG00673.hp1 HG01081.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1513-488_1513-485d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACAC | T | 18 | a0001c0001t0001g0123a0001c0001t0001g0137a0001c0001t0001g0151others(15): Show | 18 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.1513-490_1513-485d others(8): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACACA others(1): Show |
T | 40 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0149others(37): Show | 41 | HG00280.hp2 HG00673.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.1513-492_1513-485d others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACACA others(3): Show |
T | 3 | a0001c0002t0001g0011a0001c0002t0001g0044a0001c0004t0001g0107 | 3 | HG02071.hp2 HG03471.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1513-494_1513-485d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACACA others(5): Show |
T | 7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0103others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1513-496_1513-485d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACACA others(9): Show |
T | 1 | a0001c0001t0001g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1513-500_1513-485d others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACACA others(11): Show |
T | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1513-502_1513-485d others(20): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1513-506_1513-485d others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450844
|
TACACACA others(17): Show |
T | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1513-508_1513-485d others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450844 | ||||||
| chr22:31450846
|
CACACACA others(2): Show |
C | 4 | a0001c0001t0001g0212a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG02717.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1513-495_1513-487d others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450846 | ||||||
| chr22:31450846
|
CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513-497_1513-487d others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450846 | ||||||
| chr22:31450852
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0353 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1513-492G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450852 | ||||||
| chr22:31450854
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0258 | 2 | HG00738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1513-494G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450854 | ||||||
| chr22:31450856
|
C | T | 4 | a0001c0001t0001g0212a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG02717.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1513-496G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450856 | ||||||
| chr22:31450858
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513-498G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450858 | ||||||
| chr22:31450864
|
C | G | 1 | a0001c0002t0001g0064 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1513-504G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450864 | ||||||
| chr22:31450884
|
CACACACA others(5): Show |
C | 3 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0007t0001g0108 | 3 | HG02109.hp2 HG02630.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1513-536_1513-525d others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450884 | ||||||
| chr22:31450886
|
CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0117a0001c0007t0001g0363 | 2 | HG02965.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1513-536_1513-527d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450886 | ||||||
| chr22:31450895
|
A | ACACAC | 3 | a0001c0001t0001g0227a0001c0001t0001g0243a0001c0003t0001g0345 | 3 | HG00735.hp2 HG02135.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1513-536_1513-535i others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450895 | ||||||
| chr22:31450896
|
A | C | 22 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0224others(19): Show | 22 | HG00408.hp2 HG00609.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1513-536T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450896 | ||||||
| chr22:31450898
|
A | C | 4 | a0001c0001t0002g0267a0001c0001t0002g0272a0001c0001t0002g0283others(1): Show | 4 | HG01346.hp1 HG02895.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1513-538T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31450898 | ||||||
| chr22:31451083
|
G | A | 3 | a0001c0003t0001g0124a0001c0003t0001g0290a0001c0003t0001g0294 | 3 | HG00741.hp1 HG01361.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1513-723C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451083 | ||||||
| chr22:31451275
|
T | C | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1513-915A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451275 | ||||||
| chr22:31451337
|
G | C | 2 | a0001c0003t0001g0331a0001c0003t0001g0341 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1513-977C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451337 | ||||||
| chr22:31451383
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1513-1023G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451383 | ||||||
| chr22:31451440
|
AT | A | 6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0250others(3): Show | 6 | HG01169.hp1 HG02055.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1513-1081delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451440 | ||||||
| chr22:31451569
|
C | T | 1 | a0001c0003t0001g0352 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1513-1209G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451569 | ||||||
| chr22:31451661
|
T | C | 116 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1513-1301A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451661 | ||||||
| chr22:31451664
|
C | CT | 9 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0192others(6): Show | 9 | HG02145.hp2 HG02965.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1513-1305dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451664 | ||||||
| chr22:31451664
|
C | G | 1 | a0001c0001t0001g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1513-1304G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451664 | ||||||
| chr22:31451665
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513-1305A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451665 | ||||||
| chr22:31451864
|
C | G | 68 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0009others(65): Show | 69 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1513-1504G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451864 | ||||||
| chr22:31451926
|
A | C | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1513-1566T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31451926 | ||||||
| chr22:31452077
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1513-1717C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452077 | ||||||
| chr22:31452165
|
T | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1513-1805A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452165 | ||||||
| chr22:31452231
|
T | G | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1513-1871A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452231 | ||||||
| chr22:31452385
|
A | C | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1512+1759T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452385 | ||||||
| chr22:31452578
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0138 | 2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1512+1566G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452578 | ||||||
| chr22:31452639
|
C | G | 8 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1512+1505G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452639 | ||||||
| chr22:31452739
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1512+1405C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452739 | ||||||
| chr22:31452805
|
G | T | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+1339C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452805 | ||||||
| chr22:31452806
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG02109.hp2 HG02630.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1512+1338C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452806 | ||||||
| chr22:31452958
|
A | G | 68 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0009others(65): Show | 69 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1512+1186T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31452958 | ||||||
| chr22:31453036
|
G | GA | 116 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1512+1107dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453036 | ||||||
| chr22:31453044
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+1100C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453044 | ||||||
| chr22:31453045
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+1099T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453045 | ||||||
| chr22:31453165
|
T | C | 1 | a0001c0003t0001g0269 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1512+979A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453165 | ||||||
| chr22:31453278
|
CCTAACTT others(4): Show |
C | 1 | a0001c0003t0001g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1512+855_1512+865d others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453278 | ||||||
| chr22:31453291
|
C | A | 1 | a0001c0003t0001g0313 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1512+853G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453291 | ||||||
| chr22:31453376
|
C | CT | 7 | a0001c0001t0001g0050a0001c0001t0001g0169a0001c0001t0001g0192others(4): Show | 7 | HG02040.hp2 HG03209.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1512+767dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453376 | ||||||
| chr22:31453444
|
G | A | 1 | a0001c0002t0001g0013 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1512+700C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453444 | ||||||
| chr22:31453489
|
C | T | 5 | a0001c0003t0001g0299a0001c0003t0001g0300a0001c0003t0001g0301others(2): Show | 5 | HG01884.hp2 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1512+655G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453489 | ||||||
| chr22:31453557
|
G | A | 1 | a0001c0002t0001g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1512+587C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453557 | ||||||
| chr22:31453652
|
C | T | 20 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(17): Show | 20 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1512+492G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453652 | ||||||
| chr22:31453984
|
A | G | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361 | 3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1512+160T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31453984 | ||||||
| chr22:31454078
|
T | A | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1512+66A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31454078 | ||||||
| chr22:31454137
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02717.hp1 | splice_region_variant&intron_variant | LOW | c.1512+7A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 10/18 | chr22 | 31454137 | ||||||
| chr22:31454447
|
T | G | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1280-71A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454447 | ||||||
| chr22:31454621
|
A | G | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280-245T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454621 | ||||||
| chr22:31454673
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0137 | 3 | HG01496.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1280-297A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454673 | ||||||
| chr22:31454727
|
A | C | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1280-351T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454727 | ||||||
| chr22:31454731
|
T | A | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1280-355A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454731 | ||||||
| chr22:31454745
|
G | A | 1 | a0001c0002t0001g0021 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1280-369C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454745 | ||||||
| chr22:31454775
|
G | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1279+361C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454775 | ||||||
| chr22:31454784
|
T | C | 1 | a0001c0003t0001g0343 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1279+352A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454784 | ||||||
| chr22:31454832
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1279+304C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454832 | ||||||
| chr22:31454905
|
A | AC | 116 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(113): Show | 116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1279+230dupG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31454905 | ||||||
| chr22:31455076
|
C | T | 3 | a0001c0001t0002g0278a0001c0001t0002g0283a0001c0001t0002g0344 | 3 | HG01346.hp1 HG01934.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1279+60G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 9/18 | chr22 | 31455076 | ||||||
| chr22:31455362
|
G | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1100-47C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455362 | ||||||
| chr22:31455382
|
T | A | 3 | a0001c0003t0001g0269a0001c0003t0001g0296a0001c0003t0006g0364 | 3 | HG01358.hp2 HG03490.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1100-67A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455382 | ||||||
| chr22:31455395
|
CT | C | 59 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0120others(56): Show | 59 | HG00408.hp1 HG00423.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.1100-81delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455395 | ||||||
| chr22:31455399
|
T | C | 5 | a0001c0003t0001g0335a0001c0005t0001g0144a0001c0005t0001g0145others(2): Show | 5 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100-84A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455399 | ||||||
| chr22:31455400
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0189 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1100-85A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455400 | ||||||
| chr22:31455467
|
C | T | 71 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0050others(68): Show | 71 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1100-152G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455467 | ||||||
| chr22:31455502
|
G | A | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1100-187C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455502 | ||||||
| chr22:31455608
|
C | A | 9 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1099+244G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 8/18 | chr22 | 31455608 | ||||||
| chr22:31456091
|
C | T | 1 | a0001c0002t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.964-104G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456091 | ||||||
| chr22:31456223
|
C | CT | 18 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(15): Show | 18 | HG00609.hp1 HG01358.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.964-237dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456223 | ||||||
| chr22:31456223
|
CT | C | 121 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0063others(118): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.964-237delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456223 | ||||||
| chr22:31456254
|
C | T | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-267G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456254 | ||||||
| chr22:31456263
|
A | G | 3 | a0001c0001t0001g0134a0001c0006t0001g0142a0001c0006t0001g0176 | 3 | HG02738.hp2 NA18992.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.964-276T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456263 | ||||||
| chr22:31456264
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.964-277G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456264 | ||||||
| chr22:31456285
|
A | G | 2 | a0001c0003t0001g0017a0001c0003t0001g0338 | 2 | HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.964-298T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456285 | ||||||
| chr22:31456287
|
G | A | 2 | a0001c0003t0001g0017a0001c0003t0001g0338 | 2 | HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.964-300C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456287 | ||||||
| chr22:31456309
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.964-322G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456309 | ||||||
| chr22:31456325
|
A | G | 5 | a0001c0003t0001g0124a0001c0003t0001g0287a0001c0003t0001g0290others(2): Show | 5 | HG00741.hp1 HG01361.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-338T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456325 | ||||||
| chr22:31456336
|
G | A | 1 | a0001c0003t0001g0124 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.964-349C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456336 | ||||||
| chr22:31456368
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.964-381G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456368 | ||||||
| chr22:31456372
|
T | C | 31 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0128others(28): Show | 31 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.964-385A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456372 | ||||||
| chr22:31456373
|
G | A | 1 | a0001c0002t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.964-386C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456373 | ||||||
| chr22:31456379
|
A | G | 1 | a0001c0002t0001g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.964-392T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456379 | ||||||
| chr22:31456380
|
C | T | 26 | a0001c0001t0001g0233a0001c0001t0002g0265a0001c0001t0002g0266others(23): Show | 26 | HG00408.hp2 HG00609.hp1 HG01928.hp2 others(23): Show |
intron_variant | MODIFIER | c.964-393G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456380 | ||||||
| chr22:31456381
|
G | A | 2 | a0001c0002t0001g0012a0001c0002t0001g0060 | 2 | HG03654.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.964-394C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456381 | ||||||
| chr22:31456382
|
C | T | 1 | a0001c0002t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.964-395G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456382 | ||||||
| chr22:31456421
|
T | C | 199 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0030others(196): Show | 200 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.964-434A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456421 | ||||||
| chr22:31456424
|
C | T | 1 | a0001c0003t0001g0318 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.964-437G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456424 | ||||||
| chr22:31456425
|
G | A | 4 | a0001c0001t0001g0005a0001c0002t0001g0029a0001c0002t0001g0051others(1): Show | 4 | HG00609.hp2 HG02074.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-438C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456425 | ||||||
| chr22:31456430
|
A | G | 3 | a0001c0002t0001g0059a0001c0003t0001g0288a0001c0003t0001g0291 | 3 | HG00140.hp2 HG01257.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.964-443T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456430 | ||||||
| chr22:31456434
|
A | G | 1 | a0001c0002t0001g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.964-447T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456434 | ||||||
| chr22:31456438
|
T | G | 2 | a0001c0002t0001g0051a0001c0002t0001g0052 | 2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.964-451A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456438 | ||||||
| chr22:31456439
|
G | C | 133 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00408.hp2 HG00544.hp1 HG00673.hp2 others(130): Show |
intron_variant | MODIFIER | c.964-452C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456439 | ||||||
| chr22:31456441
|
T | C | 111 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0140others(108): Show | 111 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.964-454A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456441 | ||||||
| chr22:31456444
|
C | T | 2 | a0001c0001t0001g0212a0005c0012t0001g0035 | 2 | NA18995.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.964-457G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456444 | ||||||
| chr22:31456445
|
G | C | 7 | a0001c0001t0002g0270a0001c0001t0002g0281a0001c0002t0001g0001others(4): Show | 8 | HG00280.hp2 HG01891.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-458C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456445 | ||||||
| chr22:31456458
|
T | C | 3 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0038 | 3 | NA18948.hp2 NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.964-471A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456458 | ||||||
| chr22:31456465
|
C | T | 2 | a0001c0001t0002g0270a0001c0001t0002g0281 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.964-478G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456465 | ||||||
| chr22:31456500
|
A | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0050others(122): Show | 127 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.964-513T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456500 | ||||||
| chr22:31456503
|
A | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0055others(118): Show | 123 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.964-516T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456503 | ||||||
| chr22:31456512
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.964-525G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456512 | ||||||
| chr22:31456513
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0284a0001c0001t0002g0272others(1): Show | 5 | HG02965.hp1 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-526T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456513 | ||||||
| chr22:31456515
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0284a0001c0002t0001g0058 | 4 | HG02965.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-528T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456515 | ||||||
| chr22:31456618
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.964-631C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456618 | ||||||
| chr22:31456649
|
G | A | 339 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0024others(336): Show | 340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.964-662C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456649 | ||||||
| chr22:31456717
|
A | T | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.964-730T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456717 | ||||||
| chr22:31456718
|
C | A | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.964-731G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456718 | ||||||
| chr22:31456721
|
T | C | 1 | a0001c0005t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.964-734A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31456721 | ||||||
| chr22:31457022
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.964-1035A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457022 | ||||||
| chr22:31457033
|
T | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0133 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.964-1046A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457033 | ||||||
| chr22:31457104
|
A | T | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-1117T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457104 | ||||||
| chr22:31457126
|
T | G | 21 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(18): Show | 21 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.964-1139A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457126 | ||||||
| chr22:31457239
|
T | C | 68 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0009others(65): Show | 69 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.963+1236A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457239 | ||||||
| chr22:31457291
|
G | A | 1 | a0001c0002t0001g0051 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.963+1184C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457291 | ||||||
| chr22:31457385
|
A | C | 118 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.963+1090T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457385 | ||||||
| chr22:31457455
|
C | G | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+1020G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457455 | ||||||
| chr22:31457498
|
G | A | 10 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+977C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457498 | ||||||
| chr22:31457532
|
T | C | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.963+943A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457532 | ||||||
| chr22:31457533
|
C | A | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.963+942G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457533 | ||||||
| chr22:31457836
|
G | A | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.963+639C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457836 | ||||||
| chr22:31457867
|
C | T | 1 | a0001c0001t0002g0268 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.963+608G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457867 | ||||||
| chr22:31457877
|
A | G | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+598T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457877 | ||||||
| chr22:31457905
|
A | G | 1 | a0001c0003t0001g0356 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.963+570T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31457905 | ||||||
| chr22:31458223
|
A | G | 167 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(164): Show | 167 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.963+252T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458223 | ||||||
| chr22:31458227
|
C | CA | 73 | a0001c0001t0001g0090a0001c0001t0001g0205a0001c0001t0001g0262others(70): Show | 74 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.963+247dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458227 | ||||||
| chr22:31458244
|
C | A | 136 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(133): Show | 136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.963+231G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458244 | ||||||
| chr22:31458298
|
C | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+177G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458298 | ||||||
| chr22:31458384
|
A | G | 75 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(72): Show | 75 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.963+91T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458384 | ||||||
| chr22:31458412
|
C | T | 1 | a0001c0003t0001g0324 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.963+63G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458412 | ||||||
| chr22:31458448
|
AT | A | 342 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(339): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.963+26delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 7/18 | chr22 | 31458448 | ||||||
| chr22:31458860
|
T | C | 224 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(221): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.788-210A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458860 | ||||||
| chr22:31458918
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.788-268C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458918 | ||||||
| chr22:31458925
|
C | CT | 14 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(11): Show | 14 | HG00738.hp2 HG01993.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.788-276dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458925 | ||||||
| chr22:31458925
|
CT | C | 148 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(145): Show | 148 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.788-276delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458925 | ||||||
| chr22:31458925
|
CTT | C | 6 | a0001c0001t0001g0184a0001c0001t0001g0246a0001c0001t0001g0259others(3): Show | 6 | HG00423.hp2 HG02055.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.788-277_788-276del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31458925 | ||||||
| chr22:31459031
|
G | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-381C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459031 | ||||||
| chr22:31459076
|
C | A | 2 | a0001c0003t0001g0017a0001c0003t0001g0338 | 2 | HG03491.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.788-426G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459076 | ||||||
| chr22:31459252
|
AT | A | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-603delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459252 | ||||||
| chr22:31459262
|
T | A | 10 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.788-612A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459262 | ||||||
| chr22:31459334
|
T | C | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.788-684A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459334 | ||||||
| chr22:31459383
|
A | G | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.788-733T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459383 | ||||||
| chr22:31459453
|
G | C | 1 | a0001c0003t0001g0048 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.788-803C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459453 | ||||||
| chr22:31459489
|
T | C | 224 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(221): Show | 225 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.788-839A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459489 | ||||||
| chr22:31459501
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.788-851A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459501 | ||||||
| chr22:31459577
|
T | TG | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-928_788-927ins others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459577 | ||||||
| chr22:31459578
|
A | G | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-928T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459578 | ||||||
| chr22:31459591
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.788-941A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459591 | ||||||
| chr22:31459603
|
A | C | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.788-953T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459603 | ||||||
| chr22:31459752
|
A | ATGTTTTT others(3): Show |
317 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(314): Show | 318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.788-1112_788-1103d others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459752 | ||||||
| chr22:31459791
|
A | G | 3 | a0001c0002t0001g0019a0001c0002t0001g0025a0001c0002t0001g0038 | 3 | NA18948.hp2 NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.788-1141T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459791 | ||||||
| chr22:31459853
|
G | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-1203C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459853 | ||||||
| chr22:31459968
|
T | C | 93 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(90): Show | 94 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.788-1318A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31459968 | ||||||
| chr22:31460135
|
A | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.788-1485T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460135 | ||||||
| chr22:31460177
|
G | C | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.788-1527C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460177 | ||||||
| chr22:31460275
|
T | C | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.788-1625A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460275 | ||||||
| chr22:31460372
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.788-1722C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460372 | ||||||
| chr22:31460392
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.788-1742C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460392 | ||||||
| chr22:31460517
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0137 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.788-1867G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460517 | ||||||
| chr22:31460854
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.787+2078C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460854 | ||||||
| chr22:31460879
|
A | T | 1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.787+2053T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460879 | ||||||
| chr22:31460945
|
A | AAAAC | 10 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.787+1983_787+1986d others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31460945 | ||||||
| chr22:31461072
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.787+1860C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461072 | ||||||
| chr22:31461104
|
A | G | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.787+1828T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461104 | ||||||
| chr22:31461108
|
T | G | 1 | a0001c0002t0001g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.787+1824A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461108 | ||||||
| chr22:31461323
|
T | C | 8 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.787+1609A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461323 | ||||||
| chr22:31461448
|
G | GT | 6 | a0001c0001t0001g0008a0001c0001t0001g0202a0001c0001t0002g0265others(3): Show | 6 | HG01106.hp1 HG01361.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.787+1483dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461448 | ||||||
| chr22:31461723
|
G | A | 2 | a0001c0003t0001g0269a0001c0003t0006g0364 | 2 | HG01358.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.787+1209C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461723 | ||||||
| chr22:31461744
|
T | C | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.787+1188A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461744 | ||||||
| chr22:31461897
|
C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0060 | 2 | NA18950.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.787+1035G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461897 | ||||||
| chr22:31461913
|
T | C | 2 | a0001c0007t0001g0108a0001c0007t0001g0363 | 2 | HG02965.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.787+1019A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461913 | ||||||
| chr22:31461935
|
T | C | 1 | a0001c0005t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.787+997A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461935 | ||||||
| chr22:31461948
|
AC | A | 117 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(114): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.787+983delG | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461948 | ||||||
| chr22:31461963
|
A | T | 1 | a0001c0002t0001g0013 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.787+969T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31461963 | ||||||
| chr22:31462043
|
C | T | 10 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.787+889G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462043 | ||||||
| chr22:31462107
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0193 | 2 | NA18979.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.787+825T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462107 | ||||||
| chr22:31462206
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.787+726C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462206 | ||||||
| chr22:31462375
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787+557G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462375 | ||||||
| chr22:31462400
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.787+532C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462400 | ||||||
| chr22:31462484
|
C | CA | 215 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(212): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.787+447dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462484 | ||||||
| chr22:31462484
|
C | CAA | 17 | a0001c0001t0001g0120a0001c0001t0001g0284a0001c0001t0002g0265others(14): Show | 17 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.787+446_787+447dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462484 | ||||||
| chr22:31462753
|
T | A | 1 | a0001c0001t0002g0282 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.787+179A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 6/18 | chr22 | 31462753 | ||||||
| chr22:31463149
|
A | G | 2 | a0001c0002t0001g0083a0001c0002t0001g0086 | 2 | HG02027.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.586-16T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463149 | ||||||
| chr22:31463160
|
A | G | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.586-27T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463160 | ||||||
| chr22:31463195
|
A | G | 4 | a0001c0003t0001g0289a0001c0003t0001g0292a0001c0003t0001g0295others(1): Show | 4 | HG00323.hp2 HG01361.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.586-62T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463195 | ||||||
| chr22:31463439
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.585+242C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463439 | ||||||
| chr22:31463525
|
A | G | 10 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.585+156T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463525 | ||||||
| chr22:31463600
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.585+81G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463600 | ||||||
| chr22:31463651
|
T | TA | 137 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0055others(134): Show | 137 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.585+29dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463651 | ||||||
| chr22:31463651
|
TA | T | 17 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(14): Show | 17 | HG01070.hp1 HG01070.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.585+29delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 5/18 | chr22 | 31463651 | ||||||
| chr22:31464186
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0132 | 2 | HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.299-219C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464186 | ||||||
| chr22:31464258
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.299-291G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464258 | ||||||
| chr22:31464292
|
G | C | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.299-325C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464292 | ||||||
| chr22:31464336
|
A | G | 118 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.299-369T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464336 | ||||||
| chr22:31464496
|
GGTGAAAC others(1591): Show |
G | 2 | a0001c0003t0001g0325a0001c0003t0001g0343 | 2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.298+2081_299-530de others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464496 | ||||||
| chr22:31464555
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.299-588C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464555 | ||||||
| chr22:31464597
|
G | A | 14 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-630C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464597 | ||||||
| chr22:31464636
|
G | A | 1 | a0001c0007t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.299-669C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464636 | ||||||
| chr22:31464650
|
T | C | 1 | a0001c0002t0001g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.299-683A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464650 | ||||||
| chr22:31464655
|
A | G | 311 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(308): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.299-688T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464655 | ||||||
| chr22:31464675
|
C | CA | 12 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(9): Show | 12 | HG00408.hp2 HG01123.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-709dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
C | CAAAAA | 9 | a0001c0001t0001g0007a0001c0001t0001g0118a0001c0001t0002g0270others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-713_299-709dup others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
C | CAAAAAA | 21 | a0001c0001t0002g0271a0001c0002t0001g0001a0001c0002t0001g0010others(18): Show | 22 | HG00280.hp2 HG00673.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.299-714_299-709dup others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
C | CAAAAAAA | 7 | a0001c0002t0001g0018a0001c0002t0001g0019a0001c0002t0001g0037others(4): Show | 7 | HG01358.hp2 HG02074.hp2 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-715_299-709dup others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
C | CAAAAAAA others(3): Show |
1 | a0001c0003t0001g0354 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.299-718_299-709dup others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
C | CAAAAAAA others(4): Show |
2 | a0001c0003t0001g0335a0001c0003t0004g0323 | 2 | HG02572.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.299-719_299-709dup others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
C | CAAAAAAA others(5): Show |
2 | a0001c0003t0001g0345a0001c0003t0001g0347 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.299-720_299-709dup others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
C | CAAAAAAA others(6): Show |
1 | a0001c0003t0001g0350 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.299-721_299-709dup others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0087a0001c0001t0001g0172a0001c0001t0001g0190others(6): Show | 9 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.299-718_299-709del others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0159a0001c0001t0001g0217 | 2 | NA18940.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.299-719_299-709del others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
CAAAAAAA others(5): Show |
C | 46 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0032others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.299-720_299-709del others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464675
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0030a0001c0001t0001g0198 | 2 | HG01515.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.299-721_299-709del others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464675 | ||||||
| chr22:31464689
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0232 | 2 | HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-722T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464689 | ||||||
| chr22:31464689
|
AAAAAAAA others(5): Show |
A | 33 | a0001c0001t0001g0063a0001c0001t0001g0141a0001c0001t0001g0143others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.299-734_299-723del others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464689 | ||||||
| chr22:31464689
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0187 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.299-736_299-723del others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464689 | ||||||
| chr22:31464690
|
AAAAAAAA others(6): Show |
A | 7 | a0001c0001t0001g0157a0001c0001t0001g0164a0001c0001t0001g0166others(4): Show | 7 | HG00741.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-736_299-724del others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464690 | ||||||
| chr22:31464691
|
A | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG01928.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-724T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464691 | ||||||
| chr22:31464691
|
AAAAAAAA others(5): Show |
A | 12 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(9): Show | 12 | NA18953.hp2 NA18971.hp1 NA18972.hp2 others(9): Show |
intron_variant | MODIFIER | c.299-736_299-725del others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464691 | ||||||
| chr22:31464693
|
A | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG01928.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-726T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464693 | ||||||
| chr22:31464695
|
A | ATATATAT others(6): Show |
1 | a0001c0003t0001g0293 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.299-729_299-728ins others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464695 | ||||||
| chr22:31464695
|
A | T | 3 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG01928.hp2 HG01981.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.299-728T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464695 | ||||||
| chr22:31464697
|
A | T | 12 | a0001c0001t0001g0216a0001c0001t0001g0221a0001c0001t0001g0222others(9): Show | 12 | HG00544.hp2 HG00639.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.299-730T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464697 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(40): Show |
1 | a0001c0001t0001g0316 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(47): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(31): Show |
3 | a0001c0003t0001g0288a0001c0003t0001g0291a0001c0003t0001g0333 | 3 | HG00140.hp2 HG01257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(38): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(47): Show |
1 | a0001c0001t0001g0315 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(54): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(14): Show |
1 | a0001c0004t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(21): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(22): Show |
1 | a0005c0012t0001g0035 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(29): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0312 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(30): Show |
1 | a0002c0015t0001g0357 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(37): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(36): Show |
1 | a0001c0003t0001g0346 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(43): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(9): Show |
1 | a0001c0004t0001g0107 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(27): Show |
1 | a0001c0003t0001g0334 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(34): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0304a0001c0001t0001g0314 | 2 | NA18965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(36): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(35): Show |
3 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0003t0001g0332 | 3 | HG03831.hp1 NA18989.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(42): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(15): Show |
2 | a0001c0003t0001g0253a0001c0004t0001g0112 | 2 | HG02109.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(23): Show |
1 | a0001c0003t0001g0318 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(30): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0310 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(36): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(31): Show |
1 | a0001c0001t0001g0317 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(38): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(8): Show |
1 | a0001c0003t0001g0319 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(15): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0264 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(19): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(14): Show |
1 | a0001c0004t0001g0211 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(21): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(29): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(26): Show |
1 | a0001c0003t0001g0324 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(33): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(28): Show |
2 | a0001c0003t0001g0048a0001c0003t0001g0362 | 2 | HG01515.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(38): Show |
1 | a0001c0001t0001g0298 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(45): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(7): Show |
2 | a0001c0003t0001g0339a0003c0011t0001g0263 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0262 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(28): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(23): Show |
1 | a0001c0003t0001g0292 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(30): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(25): Show |
1 | a0001c0003t0001g0290 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(32): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0355 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(36): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(31): Show |
2 | a0001c0001t0001g0336a0001c0003t0001g0352 | 2 | HG03516.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(38): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(10): Show |
1 | a0001c0003t0001g0020 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(17): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0071 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(31): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(28): Show |
2 | a0001c0003t0001g0322a0001c0003t0001g0338 | 2 | HG01081.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(30): Show |
1 | a0001c0003t0001g0330 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(37): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0252 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(17): Show |
2 | a0001c0001t0001g0122a0001c0004t0001g0110 | 2 | HG01516.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0299 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(21): Show |
1 | a0001c0003t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(28): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(23): Show |
2 | a0001c0001t0001g0055a0001c0003t0001g0320 | 2 | HG01081.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(30): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(39): Show |
1 | a0001c0003t0001g0017 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(46): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(4): Show |
1 | a0001c0003t0001g0327 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(6): Show |
2 | a0001c0003t0001g0313a0001c0003t0001g0342 | 2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0121 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(20): Show |
1 | a0001c0003t0001g0301 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(27): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(24): Show |
1 | a0001c0003t0001g0295 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(31): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(28): Show |
1 | a0001c0003t0001g0289 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(35): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(5): Show |
3 | a0001c0003t0001g0311a0001c0003t0001g0326a0001c0003t0001g0328 | 3 | HG02895.hp2 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(12): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(7): Show |
1 | a0001c0003t0001g0349 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(11): Show |
1 | a0001c0004t0001g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0353 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(20): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0254 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(17): Show |
1 | a0001c0003t0001g0302 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(24): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0337 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(26): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAA others(27): Show |
1 | a0001c0003t0001g0285 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(34): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAT | 7 | a0001c0001t0001g0117a0001c0001t0001g0212a0001c0002t0001g0016others(4): Show | 7 | HG02074.hp1 HG06807.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-733_299-732ins others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAT others(4): Show |
1 | a0001c0002t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAT others(16): Show |
2 | a0001c0001t0001g0329a0001c0003t0001g0303 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAT others(18): Show |
1 | a0001c0003t0001g0300 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(25): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAAT others(22): Show |
2 | a0001c0003t0001g0331a0001c0003t0001g0341 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(29): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAAT | 6 | a0001c0001t0001g0151a0001c0001t0001g0210a0001c0002t0001g0043others(3): Show | 6 | HG00609.hp2 HG02132.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-733_299-732ins others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAATA others(7): Show |
2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG02717.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.299-733_299-732ins others(14): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAAATA others(11): Show |
2 | a0001c0004t0001g0111a0001c0004t0001g0115 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAATAT others(6): Show |
1 | a0001c0002t0001g0027 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAAATAT others(12): Show |
1 | a0001c0002t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(19): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAATATA others(11): Show |
1 | a0001c0001t0001g0340 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.299-733_299-732ins others(18): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAAATATA others(15): Show |
2 | a0001c0003t0001g0321a0001c0003t0001g0351 | 2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.299-733_299-732ins others(22): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | AAATATAT others(10): Show |
1 | a0001c0003t0001g0294 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(17): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.299-733_299-732ins others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464699
|
A | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(34): Show | 37 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.299-732T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464699 | ||||||
| chr22:31464700
|
AT | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0101a0001c0001t0001g0103others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-734delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464700 | ||||||
| chr22:31464701
|
T | A | 50 | a0001c0001t0001g0090a0001c0001t0001g0095a0001c0001t0001g0100others(47): Show | 50 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.299-734A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464701 | ||||||
| chr22:31464703
|
T | A | 30 | a0001c0001t0001g0088a0001c0001t0001g0103a0001c0001t0001g0104others(27): Show | 30 | HG00408.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.299-736A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464703 | ||||||
| chr22:31464703
|
T | C | 2 | a0001c0002t0001g0041a0001c0002t0001g0191 | 2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.299-736A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464703 | ||||||
| chr22:31464705
|
T | A | 17 | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0126others(14): Show | 17 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.299-738A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464705 | ||||||
| chr22:31464707
|
T | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.299-740A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464707 | ||||||
| chr22:31464713
|
T | A | 1 | a0001c0001t0002g0280 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.299-746A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464713 | ||||||
| chr22:31464725
|
T | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0137 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.299-758A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464725 | ||||||
| chr22:31464726
|
A | T | 246 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(243): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.299-759T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464726 | ||||||
| chr22:31464955
|
C | T | 22 | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0125others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-988G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464955 | ||||||
| chr22:31464997
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-1030A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31464997 | ||||||
| chr22:31465075
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299-1108C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465075 | ||||||
| chr22:31465086
|
G | C | 1 | a0001c0003t0001g0332 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.299-1119C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465086 | ||||||
| chr22:31465153
|
G | A | 2 | a0001c0001t0001g0154a0001c0002t0001g0033 | 2 | NA18951.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.299-1186C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465153 | ||||||
| chr22:31465217
|
G | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.299-1250C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465217 | ||||||
| chr22:31465224
|
G | C | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.299-1257C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465224 | ||||||
| chr22:31465323
|
C | CA | 58 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0097others(55): Show | 58 | HG00609.hp1 HG01106.hp2 HG01346.hp1 others(55): Show |
intron_variant | MODIFIER | c.299-1357dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465323 | ||||||
| chr22:31465341
|
A | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(1): Show | 4 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-1374T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465341 | ||||||
| chr22:31465373
|
G | T | 1 | a0001c0001t0002g0266 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.299-1406C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465373 | ||||||
| chr22:31465380
|
C | T | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-1413G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465380 | ||||||
| chr22:31465407
|
G | A | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.299-1440C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465407 | ||||||
| chr22:31465532
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.299-1565C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465532 | ||||||
| chr22:31465577
|
C | T | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-1610G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465577 | ||||||
| chr22:31465860
|
G | A | 68 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0009others(65): Show | 69 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.299-1893C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465860 | ||||||
| chr22:31465964
|
A | G | 234 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(231): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.299-1997T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465964 | ||||||
| chr22:31465966
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.299-1999T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31465966 | ||||||
| chr22:31466058
|
C | G | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.299-2091G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466058 | ||||||
| chr22:31466118
|
A | C | 2 | a0001c0003t0001g0325a0001c0003t0001g0343 | 2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.298+2057T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466118 | ||||||
| chr22:31466129
|
G | A | 2 | a0001c0003t0001g0325a0001c0003t0001g0343 | 2 | HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.298+2046C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466129 | ||||||
| chr22:31466178
|
T | C | 1 | a0001c0002t0001g0046 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.298+1997A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466178 | ||||||
| chr22:31466200
|
G | C | 1 | a0001c0001t0001g0183 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.298+1975C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466200 | ||||||
| chr22:31466241
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.298+1934A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466241 | ||||||
| chr22:31466290
|
A | T | 8 | a0001c0001t0001g0140a0001c0001t0001g0230a0001c0001t0001g0231others(5): Show | 8 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+1885T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466290 | ||||||
| chr22:31466319
|
G | A | 2 | a0001c0003t0001g0356a0001c0010t0001g0078 | 2 | HG03927.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.298+1856C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466319 | ||||||
| chr22:31466351
|
T | C | 4 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(1): Show | 4 | NA18612.hp2 NA18942.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+1824A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466351 | ||||||
| chr22:31466368
|
G | A | 3 | a0001c0003t0001g0326a0001c0003t0001g0327a0001c0003t0001g0328 | 3 | HG02486.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.298+1807C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466368 | ||||||
| chr22:31466415
|
TG | T | 345 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(342): Show | 346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.298+1759delC | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466415 | ||||||
| chr22:31466443
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.298+1732C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466443 | ||||||
| chr22:31466524
|
G | C | 1 | a0001c0001t0001g0250 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.298+1651C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466524 | ||||||
| chr22:31466642
|
T | C | 1 | a0001c0002t0001g0054 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.298+1533A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466642 | ||||||
| chr22:31466713
|
G | A | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+1462C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466713 | ||||||
| chr22:31466983
|
T | C | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1192A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31466983 | ||||||
| chr22:31467036
|
A | C | 118 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(115): Show | 118 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.298+1139T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467036 | ||||||
| chr22:31467049
|
A | C | 1 | a0001c0001t0001g0171 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.298+1126T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467049 | ||||||
| chr22:31467111
|
C | T | 151 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(148): Show | 151 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.298+1064G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467111 | ||||||
| chr22:31467118
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.298+1057C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467118 | ||||||
| chr22:31467139
|
T | C | 68 | a0001c0002t0001g0001a0001c0002t0001g0003a0001c0002t0001g0009others(65): Show | 69 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.298+1036A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467139 | ||||||
| chr22:31467277
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.298+898A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467277 | ||||||
| chr22:31467568
|
T | C | 10 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.298+607A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467568 | ||||||
| chr22:31467576
|
G | C | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+599C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467576 | ||||||
| chr22:31467641
|
G | A | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+534C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467641 | ||||||
| chr22:31467720
|
G | A | 1 | a0001c0002t0001g0047 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.298+455C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467720 | ||||||
| chr22:31467764
|
GA | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+410delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467764 | ||||||
| chr22:31467802
|
C | A | 1 | a0001c0002t0001g0059 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.298+373G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467802 | ||||||
| chr22:31467803
|
A | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0286 | 3 | HG01516.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.298+372T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467803 | ||||||
| chr22:31467810
|
A | C | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.298+365T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467810 | ||||||
| chr22:31467931
|
C | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0028 | 3 | HG00280.hp2 HG01106.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.298+244G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31467931 | ||||||
| chr22:31468007
|
G | A | 1 | a0001c0002t0001g0009 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.298+168C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31468007 | ||||||
| chr22:31468127
|
C | G | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+48G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 4/18 | chr22 | 31468127 | ||||||
| chr22:31468415
|
G | T | 18 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(15): Show | 18 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.171-113C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468415 | ||||||
| chr22:31468433
|
C | T | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.171-131G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468433 | ||||||
| chr22:31468703
|
A | G | 1 | a0001c0002t0001g0015 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.171-401T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468703 | ||||||
| chr22:31468890
|
A | G | 1 | a0001c0003t0001g0320 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.171-588T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31468890 | ||||||
| chr22:31469546
|
G | A | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.171-1244C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469546 | ||||||
| chr22:31469554
|
T | C | 1 | a0001c0002t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.171-1252A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469554 | ||||||
| chr22:31469648
|
A | G | 1 | a0001c0003t0001g0320 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.171-1346T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469648 | ||||||
| chr22:31469672
|
C | T | 1 | a0001c0014t0001g0116 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.171-1370G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469672 | ||||||
| chr22:31469689
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1387T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469689 | ||||||
| chr22:31469697
|
T | C | 72 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(69): Show | 73 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.171-1395A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469697 | ||||||
| chr22:31469755
|
T | C | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361 | 3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.171-1453A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31469755 | ||||||
| chr22:31470022
|
G | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.171-1720C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470022 | ||||||
| chr22:31470121
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.170+1723C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470121 | ||||||
| chr22:31470146
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008 | 3 | HG02280.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.170+1698T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470146 | ||||||
| chr22:31470161
|
C | A | 1 | a0001c0001t0001g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.170+1683G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470161 | ||||||
| chr22:31470164
|
C | CA | 36 | a0001c0001t0001g0006a0001c0001t0001g0024a0001c0001t0001g0030others(33): Show | 36 | HG00738.hp1 HG00738.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.170+1679dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470164 | ||||||
| chr22:31470164
|
CA | C | 78 | a0001c0001t0001g0092a0001c0001t0001g0100a0001c0001t0001g0102others(75): Show | 78 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.170+1679delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470164 | ||||||
| chr22:31470180
|
A | G | 71 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(68): Show | 72 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.170+1664T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470180 | ||||||
| chr22:31470181
|
A | G | 73 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.170+1663T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470181 | ||||||
| chr22:31470205
|
CT | C | 363 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(360): Show | 365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.170+1638delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470205 | ||||||
| chr22:31470250
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.170+1594C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470250 | ||||||
| chr22:31470254
|
TA | T | 363 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(360): Show | 365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.170+1589delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470254 | ||||||
| chr22:31470290
|
G | GT | 7 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+1553dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470290 | ||||||
| chr22:31470341
|
C | T | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+1503G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470341 | ||||||
| chr22:31470372
|
C | T | 15 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(12): Show | 15 | HG02040.hp2 HG02602.hp1 NA18612.hp1 others(12): Show |
intron_variant | MODIFIER | c.170+1472G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470372 | ||||||
| chr22:31470374
|
G | A | 3 | a0001c0001t0002g0270a0001c0001t0002g0271a0001c0001t0002g0281 | 3 | HG01891.hp2 HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.170+1470C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470374 | ||||||
| chr22:31470421
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.170+1423A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470421 | ||||||
| chr22:31470511
|
C | T | 10 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(7): Show | 10 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.170+1333G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470511 | ||||||
| chr22:31470629
|
A | AT | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+1214dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470629 | ||||||
| chr22:31470685
|
C | CT | 79 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0087others(76): Show | 79 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.170+1158dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470685 | ||||||
| chr22:31470685
|
C | CTT | 10 | a0001c0001t0001g0154a0001c0001t0001g0159a0001c0001t0001g0208others(7): Show | 10 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.170+1157_170+1158d others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470685 | ||||||
| chr22:31470685
|
CT | C | 13 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(10): Show | 13 | HG01516.hp1 HG01517.hp2 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.170+1158delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470685 | ||||||
| chr22:31470778
|
G | A | 1 | a0001c0007t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.170+1066C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470778 | ||||||
| chr22:31470795
|
G | A | 72 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(69): Show | 73 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.170+1049C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470795 | ||||||
| chr22:31470812
|
A | C | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+1032T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470812 | ||||||
| chr22:31470882
|
G | A | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+962C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31470882 | ||||||
| chr22:31471008
|
G | C | 1 | a0001c0003t0001g0287 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.170+836C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471008 | ||||||
| chr22:31471013
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0152 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.170+831C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471013 | ||||||
| chr22:31471053
|
A | G | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.170+791T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471053 | ||||||
| chr22:31471128
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0003t0001g0124 | 3 | HG01257.hp1 HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.170+716A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471128 | ||||||
| chr22:31471129
|
T | C | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0003t0001g0124 | 3 | HG01257.hp1 HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.170+715A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471129 | ||||||
| chr22:31471217
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.170+627C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471217 | ||||||
| chr22:31471317
|
C | CTT | 72 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056others(69): Show | 73 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.170+525_170+526dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471317 | ||||||
| chr22:31471397
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.170+447G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471397 | ||||||
| chr22:31471460
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.170+384C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471460 | ||||||
| chr22:31471717
|
C | T | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.170+127G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471717 | ||||||
| chr22:31471777
|
T | C | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.170+67A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 3/18 | chr22 | 31471777 | ||||||
| chr22:31471930
|
G | A | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-13C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31471930 | ||||||
| chr22:31472041
|
G | C | 1 | a0004c0009t0001g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-124C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472041 | ||||||
| chr22:31472057
|
G | C | 1 | a0001c0004t0001g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97-140C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472057 | ||||||
| chr22:31472069
|
T | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-152A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472069 | ||||||
| chr22:31472123
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.97-206A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472123 | ||||||
| chr22:31472125
|
C | T | 1 | a0001c0003t0001g0346 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.97-208G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472125 | ||||||
| chr22:31472168
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97-251C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472168 | ||||||
| chr22:31472237
|
T | C | 1 | a0001c0002t0001g0064 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.97-320A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472237 | ||||||
| chr22:31472269
|
GA | G | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-353delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472269 | ||||||
| chr22:31472270
|
A | AT | 80 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(77): Show | 80 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.97-354dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472270 | ||||||
| chr22:31472270
|
A | ATT | 19 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0126others(16): Show | 19 | HG01257.hp1 HG01258.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.97-355_97-354dupAA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472270 | ||||||
| chr22:31472270
|
A | ATTT | 6 | a0001c0001t0001g0106a0001c0001t0001g0125a0001c0001t0001g0138others(3): Show | 6 | HG01496.hp1 HG02055.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-356_97-354dupAA others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472270 | ||||||
| chr22:31472308
|
G | C | 1 | a0001c0001t0001g0227 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.97-391C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472308 | ||||||
| chr22:31472433
|
T | G | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.97-516A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472433 | ||||||
| chr22:31472441
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.97-524C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472441 | ||||||
| chr22:31472564
|
G | A | 2 | a0001c0003t0001g0311a0001c0003t0001g0313 | 2 | HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-647C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472564 | ||||||
| chr22:31472596
|
G | T | 1 | a0001c0010t0001g0078 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.97-679C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472596 | ||||||
| chr22:31472684
|
T | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-767A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472684 | ||||||
| chr22:31472779
|
C | T | 21 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(18): Show | 21 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.97-862G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472779 | ||||||
| chr22:31472780
|
G | C | 1 | a0001c0006t0001g0142 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.97-863C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31472780 | ||||||
| chr22:31473059
|
C | T | 1 | a0004c0009t0001g0146 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.97-1142G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473059 | ||||||
| chr22:31473063
|
C | CT | 31 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0117others(28): Show | 31 | HG00408.hp2 HG00609.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.97-1147dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473063 | ||||||
| chr22:31473063
|
CT | C | 11 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0254others(8): Show | 11 | HG00738.hp2 HG01993.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.97-1147delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473063 | ||||||
| chr22:31473075
|
T | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-1158A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473075 | ||||||
| chr22:31473201
|
C | T | 1 | a0001c0007t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.97-1284G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473201 | ||||||
| chr22:31473419
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(22): Show | 25 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.97-1502A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473419 | ||||||
| chr22:31473481
|
A | C | 73 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(70): Show | 73 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.97-1564T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473481 | ||||||
| chr22:31473679
|
GCT | G | 4 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(1): Show | 4 | NA18949.hp2 NA18979.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-1764_97-1763del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473679 | ||||||
| chr22:31473906
|
T | C | 86 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(83): Show | 86 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.97-1989A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473906 | ||||||
| chr22:31473944
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.97-2027G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31473944 | ||||||
| chr22:31474008
|
CCT | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2093_97-2092del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474008 | ||||||
| chr22:31474064
|
C | CT | 72 | a0001c0001t0001g0007a0001c0001t0001g0050a0001c0001t0001g0055others(69): Show | 73 | HG00280.hp2 HG00609.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.97-2148dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474064 | ||||||
| chr22:31474064
|
C | CTT | 8 | a0001c0001t0001g0071a0001c0002t0001g0014a0001c0002t0001g0033others(5): Show | 8 | HG00544.hp1 HG02602.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-2149_97-2148dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474064 | ||||||
| chr22:31474118
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.97-2201G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474118 | ||||||
| chr22:31474341
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97-2424C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474341 | ||||||
| chr22:31474414
|
C | T | 156 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(153): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.97-2497G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474414 | ||||||
| chr22:31474487
|
CT | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0184a0001c0001t0001g0206others(7): Show | 10 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-2571delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474487 | ||||||
| chr22:31474488
|
T | TA | 20 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(17): Show | 20 | HG00609.hp1 HG01346.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.97-2572_97-2571ins others(1): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474488 | ||||||
| chr22:31474603
|
T | C | 3 | a0001c0003t0001g0269a0001c0003t0001g0296a0001c0003t0006g0364 | 3 | HG01358.hp2 HG03490.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.97-2686A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474603 | ||||||
| chr22:31474665
|
G | A | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-2748C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474665 | ||||||
| chr22:31474733
|
C | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.97-2816G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474733 | ||||||
| chr22:31474746
|
C | T | 1 | a0001c0002t0001g0026 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.97-2829G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474746 | ||||||
| chr22:31474747
|
A | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2830T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31474747 | ||||||
| chr22:31475015
|
A | G | 1 | a0001c0007t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.97-3098T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475015 | ||||||
| chr22:31475176
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-3259A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475176 | ||||||
| chr22:31475193
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.97-3276C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475193 | ||||||
| chr22:31475202
|
T | C | 1 | a0001c0014t0001g0116 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.97-3285A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475202 | ||||||
| chr22:31475267
|
GA | G | 127 | a0001c0001t0001g0063a0001c0001t0001g0087a0001c0001t0001g0120others(124): Show | 128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.97-3351delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475267 | ||||||
| chr22:31475491
|
C | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0316 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.97-3574G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475491 | ||||||
| chr22:31475710
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0153 | 3 | HG02109.hp2 HG06807.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.97-3793C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475710 | ||||||
| chr22:31475721
|
T | TA | 109 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0001t0001g0104others(106): Show | 109 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.97-3805dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475721 | ||||||
| chr22:31475721
|
TA | T | 10 | a0001c0001t0001g0206a0001c0001t0001g0212a0001c0001t0001g0250others(7): Show | 10 | HG00738.hp2 HG01167.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-3805delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475721 | ||||||
| chr22:31475761
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.97-3844C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475761 | ||||||
| chr22:31475866
|
A | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0137 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.97-3949T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31475866 | ||||||
| chr22:31476235
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0137 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.97-4318C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476235 | ||||||
| chr22:31476463
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.97-4546G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476463 | ||||||
| chr22:31476622
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.97-4705G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476622 | ||||||
| chr22:31476669
|
T | C | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-4752A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476669 | ||||||
| chr22:31476843
|
C | CA | 109 | a0001c0001t0001g0087a0001c0001t0001g0140a0001c0001t0001g0141others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.97-4927dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476843 | ||||||
| chr22:31476891
|
T | G | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-4974A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476891 | ||||||
| chr22:31476980
|
C | CA | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0050others(6): Show | 9 | HG01358.hp2 HG02040.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-5064dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476980 | ||||||
| chr22:31476980
|
CA | C | 18 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(15): Show | 18 | HG01516.hp1 HG01517.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-5064delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476980 | ||||||
| chr22:31476996
|
A | G | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5079T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31476996 | ||||||
| chr22:31477000
|
G | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-5083C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477000 | ||||||
| chr22:31477001
|
G | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-5084C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477001 | ||||||
| chr22:31477062
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.97-5145C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477062 | ||||||
| chr22:31477118
|
C | CA | 8 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(5): Show | 8 | HG00738.hp1 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-5202dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477118 | ||||||
| chr22:31477135
|
G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0152 | 2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.97-5218C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477135 | ||||||
| chr22:31477223
|
G | C | 1 | a0001c0002t0001g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.97-5306C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477223 | ||||||
| chr22:31477286
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-5369C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477286 | ||||||
| chr22:31477301
|
A | G | 1 | a0001c0003t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.97-5384T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477301 | ||||||
| chr22:31477315
|
T | C | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-5398A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477315 | ||||||
| chr22:31477357
|
C | CA | 96 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(93): Show | 97 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.97-5441dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477357 | ||||||
| chr22:31477357
|
C | CAA | 20 | a0001c0001t0001g0005a0001c0001t0001g0149a0001c0001t0001g0210others(17): Show | 20 | HG00609.hp2 HG01978.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.97-5442_97-5441dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477357 | ||||||
| chr22:31477357
|
CA | C | 18 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118others(15): Show | 18 | HG00738.hp2 HG01993.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-5441delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477357 | ||||||
| chr22:31477366
|
A | C | 8 | a0001c0004t0001g0107a0001c0004t0001g0110a0001c0004t0001g0111others(5): Show | 8 | HG02109.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.97-5449T>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477366 | ||||||
| chr22:31477367
|
AAAAAAAA others(10): Show |
A | 1 | a0001c0003t0001g0269 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.97-5467_97-5451del others(17): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477367 | ||||||
| chr22:31477369
|
AAAAAAC | A | 57 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0286others(54): Show | 57 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.97-5458_97-5453del others(6): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477369 | ||||||
| chr22:31477370
|
AAAAAC | A | 36 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0284others(33): Show | 36 | HG00408.hp2 HG00609.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.97-5458_97-5454del others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477370 | ||||||
| chr22:31477373
|
AACAAAAA others(4): Show |
A | 1 | a0001c0003t0001g0349 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.97-5467_97-5457del others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477373 | ||||||
| chr22:31477374
|
ACAAAAAA others(3): Show |
A | 1 | a0001c0003t0001g0276 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.97-5467_97-5458del others(10): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477374 | ||||||
| chr22:31477375
|
C | A | 194 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(191): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.97-5458G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477375 | ||||||
| chr22:31477384
|
C | A | 106 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 106 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.97-5467G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477384 | ||||||
| chr22:31477390
|
A | G | 101 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(98): Show | 101 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.97-5473T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477390 | ||||||
| chr22:31477466
|
C | G | 1 | a0001c0001t0002g0273 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.97-5549G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477466 | ||||||
| chr22:31477700
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97-5783G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477700 | ||||||
| chr22:31477852
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.97-5935C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31477852 | ||||||
| chr22:31478122
|
T | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0260a0001c0001t0001g0261 | 3 | HG01109.hp1 HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.97-6205A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478122 | ||||||
| chr22:31478288
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-6371C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478288 | ||||||
| chr22:31478295
|
C | T | 1 | a0001c0003t0001g0320 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.97-6378G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478295 | ||||||
| chr22:31478356
|
T | TA | 109 | a0001c0001t0001g0087a0001c0001t0001g0140a0001c0001t0001g0141others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.97-6440dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478356 | ||||||
| chr22:31478370
|
G | A | 1 | a0001c0001t0002g0282 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.97-6453C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478370 | ||||||
| chr22:31478475
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.97-6558G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478475 | ||||||
| chr22:31478515
|
C | CA | 198 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0030others(195): Show | 199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.97-6599dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | ||||||
| chr22:31478515
|
C | CAA | 14 | a0001c0001t0001g0024a0001c0001t0001g0158a0001c0001t0001g0159others(11): Show | 14 | HG01261.hp2 HG01981.hp1 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.97-6600_97-6599dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | ||||||
| chr22:31478515
|
C | CAAA | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | HG01168.hp2 HG01496.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.97-6601_97-6599dup others(3): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | ||||||
| chr22:31478515
|
C | CAAAA | 84 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(81): Show | 84 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.97-6602_97-6599dup others(4): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | ||||||
| chr22:31478515
|
C | CAAAAA | 16 | a0001c0001t0001g0264a0001c0001t0001g0298a0001c0001t0001g0304others(13): Show | 16 | HG01346.hp1 HG01358.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.97-6603_97-6599dup others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478515 | ||||||
| chr22:31478722
|
C | T | 62 | a0001c0001t0001g0087a0001c0001t0001g0141a0001c0001t0001g0143others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.97-6805G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478722 | ||||||
| chr22:31478778
|
C | T | 74 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0286others(71): Show | 74 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.97-6861G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478778 | ||||||
| chr22:31478808
|
C | T | 7 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(4): Show | 7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-6891G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478808 | ||||||
| chr22:31478820
|
C | T | 7 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(4): Show | 7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-6903G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478820 | ||||||
| chr22:31478835
|
C | T | 2 | a0001c0001t0001g0106a0001c0007t0001g0108 | 2 | HG02809.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.97-6918G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478835 | ||||||
| chr22:31478921
|
C | T | 1 | a0001c0005t0001g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.97-7004G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478921 | ||||||
| chr22:31478949
|
C | CA | 125 | a0001c0001t0001g0087a0001c0001t0001g0097a0001c0001t0001g0120others(122): Show | 125 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.97-7033dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478949 | ||||||
| chr22:31478949
|
C | CAA | 9 | a0001c0001t0001g0194a0001c0001t0001g0207a0001c0001t0001g0213others(6): Show | 9 | HG00323.hp1 HG00741.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-7034_97-7033dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478949 | ||||||
| chr22:31478949
|
CA | C | 7 | a0001c0001t0001g0286a0001c0001t0001g0305a0001c0001t0001g0306others(4): Show | 7 | HG01516.hp2 HG02602.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-7033delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31478949 | ||||||
| chr22:31479031
|
AGACAGAT | A | 109 | a0001c0001t0001g0087a0001c0001t0001g0140a0001c0001t0001g0141others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.97-7121_97-7115del others(7): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479031 | ||||||
| chr22:31479237
|
T | C | 1 | a0001c0002t0001g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.97-7320A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479237 | ||||||
| chr22:31479322
|
A | G | 62 | a0001c0001t0001g0087a0001c0001t0001g0141a0001c0001t0001g0143others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.97-7405T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479322 | ||||||
| chr22:31479668
|
A | G | 7 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(4): Show | 7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.97-7751T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479668 | ||||||
| chr22:31479687
|
G | GT | 7 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(4): Show | 7 | HG02056.hp1 HG02148.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-7771dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479687 | ||||||
| chr22:31479687
|
GT | G | 217 | a0001c0001t0001g0087a0001c0001t0001g0099a0001c0001t0001g0102others(214): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.97-7771delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479687 | ||||||
| chr22:31479687
|
GTT | G | 11 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 11 | HG00323.hp1 HG01515.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-7772_97-7771del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479687 | ||||||
| chr22:31479792
|
C | T | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-7875G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479792 | ||||||
| chr22:31479803
|
T | C | 1 | a0001c0002t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.97-7886A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479803 | ||||||
| chr22:31479890
|
T | G | 5 | a0001c0003t0001g0299a0001c0003t0001g0300a0001c0003t0001g0301others(2): Show | 5 | HG01884.hp2 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-7973A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31479890 | ||||||
| chr22:31480279
|
T | C | 1 | a0001c0002t0001g0061 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.96+8344A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480279 | ||||||
| chr22:31480415
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0224 | 2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.96+8208T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480415 | ||||||
| chr22:31480458
|
T | G | 3 | a0001c0002t0001g0010a0001c0002t0001g0011a0001c0002t0001g0062 | 3 | HG03239.hp1 HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.96+8165A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480458 | ||||||
| chr22:31480480
|
G | A | 222 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0121others(219): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.96+8143C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480480 | ||||||
| chr22:31480522
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.96+8101C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480522 | ||||||
| chr22:31480624
|
G | T | 1 | a0001c0002t0001g0022 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.96+7999C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480624 | ||||||
| chr22:31480711
|
C | A | 1 | a0001c0002t0001g0013 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.96+7912G>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480711 | ||||||
| chr22:31480750
|
C | G | 1 | a0001c0001t0001g0217 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.96+7873G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480750 | ||||||
| chr22:31480807
|
G | A | 1 | a0001c0006t0001g0203 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.96+7816C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31480807 | ||||||
| chr22:31481032
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.96+7591G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481032 | ||||||
| chr22:31481145
|
T | C | 1 | a0001c0003t0001g0337 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.96+7478A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481145 | ||||||
| chr22:31481185
|
CAG | C | 81 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(78): Show | 82 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+7436_96+7437del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481185 | ||||||
| chr22:31481328
|
A | AT | 12 | a0001c0001t0001g0008a0001c0001t0001g0106a0001c0001t0001g0133others(9): Show | 12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+7294dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481328 | ||||||
| chr22:31481328
|
AT | A | 211 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0121others(208): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.96+7294delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481328 | ||||||
| chr22:31481471
|
CTTAAA | C | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | HG01496.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+7147_96+7151del others(5): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481471 | ||||||
| chr22:31481518
|
C | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0221a0001c0001t0001g0222others(1): Show | 4 | HG01928.hp1 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+7105G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481518 | ||||||
| chr22:31481771
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.96+6852C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481771 | ||||||
| chr22:31481786
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.96+6837G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481786 | ||||||
| chr22:31481798
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.96+6825T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31481798 | ||||||
| chr22:31482066
|
G | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0256others(1): Show | 4 | HG01934.hp2 HG02293.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+6557C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482066 | ||||||
| chr22:31482165
|
C | CA | 101 | a0001c0001t0001g0087a0001c0001t0001g0105a0001c0001t0001g0125others(98): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.96+6457dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482165 | ||||||
| chr22:31482165
|
CA | C | 6 | a0001c0001t0001g0149a0001c0001t0002g0273a0001c0001t0002g0274others(3): Show | 6 | HG00609.hp1 HG01168.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+6457delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482165 | ||||||
| chr22:31482233
|
C | T | 1 | a0001c0001t0002g0272 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.96+6390G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482233 | ||||||
| chr22:31482271
|
T | A | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.96+6352A>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482271 | ||||||
| chr22:31482362
|
A | G | 8 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG01123.hp1 HG01261.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.96+6261T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482362 | ||||||
| chr22:31482419
|
C | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0264a0003c0011t0001g0263 | 3 | HG02055.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.96+6204G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482419 | ||||||
| chr22:31482438
|
T | C | 4 | a0001c0002t0001g0065a0001c0002t0001g0066a0001c0002t0001g0067others(1): Show | 4 | NA18612.hp2 NA18942.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+6185A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482438 | ||||||
| chr22:31482442
|
C | CA | 3 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+6180dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482442 | ||||||
| chr22:31482576
|
G | A | 14 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(11): Show | 14 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.96+6047C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482576 | ||||||
| chr22:31482595
|
T | C | 109 | a0001c0001t0001g0087a0001c0001t0001g0140a0001c0001t0001g0141others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.96+6028A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482595 | ||||||
| chr22:31482673
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.96+5950G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482673 | ||||||
| chr22:31482691
|
C | CA | 7 | a0001c0001t0001g0125a0001c0001t0001g0138a0001c0001t0001g0204others(4): Show | 7 | HG02055.hp2 HG03654.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+5931dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482691 | ||||||
| chr22:31482723
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+5900C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482723 | ||||||
| chr22:31482894
|
C | T | 5 | a0001c0003t0001g0299a0001c0003t0001g0300a0001c0003t0001g0301others(2): Show | 5 | HG01884.hp2 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+5729G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31482894 | ||||||
| chr22:31483205
|
C | T | 359 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(356): Show | 361 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.96+5418G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483205 | ||||||
| chr22:31483209
|
C | CT | 125 | a0001c0001t0001g0004a0001c0001t0001g0087a0001c0001t0001g0091others(122): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.96+5413dupA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483209 | ||||||
| chr22:31483209
|
C | CTT | 8 | a0001c0001t0001g0125a0001c0001t0001g0138a0001c0001t0001g0214others(5): Show | 8 | HG01361.hp2 HG02055.hp2 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.96+5412_96+5413dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483209 | ||||||
| chr22:31483209
|
CT | C | 15 | a0001c0001t0001g0071a0001c0001t0001g0254a0001c0001t0001g0340others(12): Show | 15 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+5413delA | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483209 | ||||||
| chr22:31483255
|
A | G | 81 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(78): Show | 82 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+5368T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483255 | ||||||
| chr22:31483479
|
A | G | 109 | a0001c0001t0001g0087a0001c0001t0001g0140a0001c0001t0001g0141others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.96+5144T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483479 | ||||||
| chr22:31483549
|
A | G | 2 | a0001c0003t0001g0269a0001c0003t0006g0364 | 2 | HG01358.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.96+5074T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483549 | ||||||
| chr22:31483551
|
C | T | 4 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(1): Show | 4 | NA18949.hp2 NA18979.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+5072G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483551 | ||||||
| chr22:31483689
|
G | C | 343 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(340): Show | 344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.96+4934C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483689 | ||||||
| chr22:31483783
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.96+4840G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31483783 | ||||||
| chr22:31484258
|
G | A | 1 | a0001c0002t0001g0072 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.96+4365C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484258 | ||||||
| chr22:31484447
|
G | A | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+4176C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484447 | ||||||
| chr22:31484494
|
A | G | 1 | a0001c0002t0001g0015 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.96+4129T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484494 | ||||||
| chr22:31484540
|
TA | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0154a0001c0001t0001g0213others(4): Show | 7 | HG00323.hp1 HG03491.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+4082delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484540 | ||||||
| chr22:31484631
|
T | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.96+3992A>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484631 | ||||||
| chr22:31484653
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.96+3970C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484653 | ||||||
| chr22:31484761
|
GGCGGAGG others(9): Show |
G | 1 | a0001c0001t0001g0089 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.96+3846_96+3861del others(16): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484761 | ||||||
| chr22:31484763
|
C | T | 81 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(78): Show | 82 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+3860G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484763 | ||||||
| chr22:31484884
|
C | T | 2 | a0001c0001t0001g0153a0001c0002t0001g0012 | 2 | HG03654.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.96+3739G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484884 | ||||||
| chr22:31484916
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.96+3707C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484916 | ||||||
| chr22:31484949
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008 | 3 | HG02280.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.96+3674A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31484949 | ||||||
| chr22:31485081
|
T | C | 22 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267others(19): Show | 22 | HG00408.hp2 HG00609.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+3542A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485081 | ||||||
| chr22:31485183
|
A | G | 76 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+3440T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485183 | ||||||
| chr22:31485443
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.96+3180A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485443 | ||||||
| chr22:31485717
|
T | C | 15 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+2906A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485717 | ||||||
| chr22:31485736
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.96+2887C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485736 | ||||||
| chr22:31485747
|
T | C | 99 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0284others(96): Show | 99 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.96+2876A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485747 | ||||||
| chr22:31485843
|
C | T | 76 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0286others(73): Show | 76 | HG00140.hp2 HG00323.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.96+2780G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31485843 | ||||||
| chr22:31486007
|
G | A | 1 | a0001c0007t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+2616C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486007 | ||||||
| chr22:31486008
|
G | C | 1 | a0001c0007t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+2615C>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486008 | ||||||
| chr22:31486030
|
TGAGGTCA others(16): Show |
T | 7 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0251others(4): Show | 7 | HG00738.hp2 HG01993.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+2570_96+2592del others(23): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486030 | ||||||
| chr22:31486106
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0123a0001c0001t0001g0137 | 3 | HG01496.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.96+2517G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486106 | ||||||
| chr22:31486195
|
C | T | 81 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(78): Show | 82 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+2428G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486195 | ||||||
| chr22:31486228
|
T | C | 252 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0103others(249): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.96+2395A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486228 | ||||||
| chr22:31486279
|
A | T | 110 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(107): Show | 110 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.96+2344T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486279 | ||||||
| chr22:31486280
|
A | T | 1 | a0001c0003t0001g0356 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.96+2343T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486280 | ||||||
| chr22:31486281
|
AAAT | A | 324 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(321): Show | 325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.96+2339_96+2341del others(3): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486281 | ||||||
| chr22:31486284
|
TAA | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(19): Show | 22 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+2337_96+2338del others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486284 | ||||||
| chr22:31486286
|
A | T | 325 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0030others(322): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.96+2337T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486286 | ||||||
| chr22:31486442
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.96+2181G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486442 | ||||||
| chr22:31486519
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.96+2104C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486519 | ||||||
| chr22:31486552
|
G | A | 1 | a0001c0004t0001g0107 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+2071C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486552 | ||||||
| chr22:31486612
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02109.hp2 HG02630.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.96+2011G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486612 | ||||||
| chr22:31486799
|
G | A | 109 | a0001c0001t0001g0087a0001c0001t0001g0140a0001c0001t0001g0141others(106): Show | 109 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.96+1824C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486799 | ||||||
| chr22:31486869
|
T | C | 1 | a0001c0002t0001g0077 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.96+1754A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486869 | ||||||
| chr22:31486878
|
C | G | 1 | a0001c0003t0001g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.96+1745G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486878 | ||||||
| chr22:31486920
|
T | TA | 316 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(313): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.96+1702dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486920 | ||||||
| chr22:31486920
|
T | TAA | 6 | a0001c0001t0001g0208a0001c0001t0001g0249a0001c0001t0001g0258others(3): Show | 6 | HG00738.hp2 HG02559.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1701_96+1702dup others(2): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31486920 | ||||||
| chr22:31487031
|
T | C | 5 | a0001c0005t0001g0144a0001c0005t0001g0145a0001c0005t0001g0147others(2): Show | 5 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1592A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487031 | ||||||
| chr22:31487070
|
CA | C | 15 | a0001c0001t0001g0087a0001c0001t0001g0209a0001c0001t0001g0286others(12): Show | 15 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+1552delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487070 | ||||||
| chr22:31487070
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0259 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.96+1542_96+1552del others(11): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487070 | ||||||
| chr22:31487311
|
C | G | 1 | a0001c0001t0001g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.96+1312G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487311 | ||||||
| chr22:31487325
|
A | G | 1 | a0001c0002t0001g0013 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.96+1298T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487325 | ||||||
| chr22:31487403
|
A | G | 1 | a0001c0002t0001g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.96+1220T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487403 | ||||||
| chr22:31487620
|
T | C | 1 | a0001c0007t0001g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.96+1003A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487620 | ||||||
| chr22:31487659
|
G | A | 1 | a0001c0003t0001g0347 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.96+964C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487659 | ||||||
| chr22:31487793
|
C | CA | 29 | a0001c0001t0001g0109a0001c0001t0001g0137a0001c0001t0001g0138others(26): Show | 29 | HG00738.hp2 HG01123.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.96+829dupT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487793 | ||||||
| chr22:31487793
|
CA | C | 167 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(164): Show | 168 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.96+829delT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487793 | ||||||
| chr22:31487793
|
CAA | C | 7 | a0001c0001t0001g0143a0001c0005t0001g0144a0001c0005t0001g0145others(4): Show | 7 | HG02132.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+828_96+829delTT | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487793 | ||||||
| chr22:31487810
|
A | G | 2 | a0001c0002t0001g0010a0001c0002t0001g0011 | 2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.96+813T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487810 | ||||||
| chr22:31487865
|
C | G | 1 | a0001c0002t0001g0009 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.96+758G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487865 | ||||||
| chr22:31487982
|
T | TCTTCAAA others(8): Show |
1 | a0001c0001t0001g0259 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.96+626_96+640dupTG others(13): Show |
EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31487982 | ||||||
| chr22:31488047
|
C | T | 81 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0031others(78): Show | 82 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.96+576G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488047 | ||||||
| chr22:31488189
|
A | T | 1 | a0001c0001t0001g0141 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.96+434T>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488189 | ||||||
| chr22:31488312
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG01123.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.96+311A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488312 | ||||||
| chr22:31488419
|
T | C | 100 | a0001c0001t0001g0262a0001c0001t0001g0264a0001c0001t0001g0284others(97): Show | 100 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.96+204A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 2/18 | chr22 | 31488419 | ||||||
| chr22:31488779
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-27-34C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488779 | ||||||
| chr22:31488994
|
T | C | 1 | a0001c0001t0001g0358 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-27-249A>G | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488994 | ||||||
| chr22:31488999
|
C | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-254G>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488999 | ||||||
| chr22:31488999
|
C | T | 1 | a0001c0003t0001g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-27-254G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31488999 | ||||||
| chr22:31489076
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-27-331C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489076 | ||||||
| chr22:31489330
|
C | T | 19 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 19 | HG01070.hp2 HG01071.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28+364G>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489330 | ||||||
| chr22:31489378
|
A | G | 363 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(360): Show | 365 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-28+316T>C | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489378 | ||||||
| chr22:31489399
|
G | T | 1 | a0001c0002t0001g0003 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-28+295C>A | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489399 | ||||||
| chr22:31489418
|
G | A | 3 | a0001c0001t0001g0359a0001c0001t0001g0360a0001c0001t0001g0361 | 3 | NA19012.hp2 NA19063.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-28+276C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489418 | ||||||
| chr22:31489509
|
G | A | 1 | a0001c0003t0001g0362 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-28+185C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489509 | ||||||
| chr22:31489531
|
G | A | 1 | a0001c0007t0001g0363 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-28+163C>T | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489531 | ||||||
| chr22:31489646
|
CG | C | 245 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-28+47delC | EIF4ENIF1 | ENSG00000184708.18 | transcript | ENST00000330125.10 | protein_coding | 1/18 | chr22 | 31489646 |