Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1981 |
| ensemblid | ENSG00000114867.22 |
| hgncid | 3296 |
| symbol | EIF4G1 |
| name | eukaryotic translation initiation factor 4 gamma 1 |
| refseq_nuc | NM_198241.3 |
| refseq_prot | NP_937884.2 |
| ensembl_nuc | ENST00000346169.7 |
| ensembl_prot | ENSP00000316879.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 184314606 |
| end | 184335353 |
| strand | + |
| ver | v1.2 |
| region | chr3:184314606-184335353 |
| region5000 | chr3:184309606-184340353 |
| regionname0 | EIF4G1_chr3_184314606_184335353 |
| regionname5000 | EIF4G1_chr3_184309606_184340353 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1599 | 278 | 81 | 41 | 114 | 15 | 27 | 86 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0002 | 1/0 | 1599 | 86 | 2 | 10 | 58 | 3 | 12 | 44 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0003 | 0/0 | 1596 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1591): Show |
chr3 | 184309606 | 184340353 |
| a0004 | 0/0 | 1599 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0005 | 0/0 | 1599 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0006 | 0/0 | 1599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0007 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0008 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0009 | 0/0 | 1599 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0010 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0011 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0012 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| a0013 | 0/1 | 1599 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | MNKAP others(1594): Show |
chr3 | 184309606 | 184340353 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 4797 | 227 | 71 | 31 | 105 | 8 | 12 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0001c0003 | 0/0 | 4797 | 38 | 5 | 8 | 7 | 4 | 14 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0001c0006 | 0/0 | 4797 | 4 | 1 | 0 | 2 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0001c0007 | 0/0 | 4797 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0001c0010 | 0/0 | 4797 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0001c0011 | 0/0 | 4797 | 2 | 0 | 0 | 0 | 2 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0001c0017 | 0/0 | 4797 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0001c0019 | 0/0 | 4797 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0002c0002 | 1/0 | 4797 | 77 | 2 | 10 | 49 | 3 | 12 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0002c0004 | 0/0 | 4797 | 8 | 0 | 0 | 8 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0002c0014 | 0/0 | 4797 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0003c0005 | 0/0 | 4788 | 5 | 0 | 5 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4783): Show |
chr3 | 184309606 | 184340353 | ||
| a0004c0008 | 0/0 | 4797 | 3 | 2 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0004c0023 | 0/0 | 4797 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0005c0009 | 0/0 | 4797 | 2 | 1 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0005c0015 | 0/0 | 4797 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0006c0013 | 0/0 | 4797 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0007c0021 | 0/0 | 4797 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0008c0012 | 0/0 | 4797 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0009c0022 | 0/0 | 4797 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0010c0016 | 0/0 | 4797 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0011c0020 | 0/0 | 4797 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0012c0018 | 0/0 | 4797 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 | ||
| a0013c0024 | 0/1 | 4797 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | ATGAA others(4792): Show |
chr3 | 184309606 | 184340353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5405 | 223 | 71 | 31 | 101 | 8 | 12 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0001t0004 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0001t0005 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0001t0006 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0001t0008 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0003t0001 | 0/0 | 5405 | 38 | 5 | 8 | 7 | 4 | 14 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0006t0001 | 0/0 | 5405 | 2 | 1 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0006t0003 | 0/0 | 5405 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0007t0002 | 0/0 | 5405 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0010t0001 | 0/0 | 5405 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0011t0001 | 0/0 | 5405 | 2 | 0 | 0 | 0 | 2 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0017t0007 | 0/0 | 5405 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0001c0019t0001 | 0/0 | 5405 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0002c0002t0001 | 1/0 | 5405 | 77 | 2 | 10 | 49 | 3 | 12 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0002c0004t0001 | 0/0 | 5405 | 8 | 0 | 0 | 8 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0002c0014t0001 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0003c0005t0001 | 0/0 | 5396 | 5 | 0 | 5 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5391): Show |
chr3 | 184309606 | 184340353 |
| a0004c0008t0001 | 0/0 | 5405 | 3 | 2 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0004c0023t0001 | 0/0 | 5405 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0005c0009t0001 | 0/0 | 5405 | 2 | 1 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0005c0015t0001 | 0/0 | 5405 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0006c0013t0001 | 0/0 | 5405 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0007c0021t0001 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0008c0012t0001 | 0/0 | 5405 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0009c0022t0001 | 0/0 | 5405 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0010c0016t0001 | 0/0 | 5405 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0011c0020t0001 | 0/0 | 5405 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0012c0018t0001 | 0/0 | 5405 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| a0013c0024t0001 | 0/1 | 5405 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | GGAAA others(5400): Show |
chr3 | 184309606 | 184340353 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 63 | 7 | 10 | 42 | 1 | 3 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0003 | 0/0 | 31 | 4 | 0 | 24 | 2 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0005 | 0/0 | 13 | 3 | 5 | 0 | 2 | 3 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0007 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0004 | 0/0 | 19 | 1 | 4 | 3 | 3 | 8 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0008 | 0/0 | 8 | 0 | 1 | 3 | 0 | 4 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0006t0001g0012 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0006t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0007t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0007t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0010t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0011t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0017t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0001c0019t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0002 | 1/0 | 49 | 2 | 8 | 25 | 3 | 10 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0004t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0002c0014t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0003c0005t0001g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0003c0005t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0004c0008t0001g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0004c0023t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0005c0009t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0005c0015t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0006c0013t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0007c0021t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0008c0012t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0009c0022t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0010c0016t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0011c0020t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0012c0018t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| a0013c0024t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0004 | EUR | GBR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0036 | EUR | GBR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0004 | EUR | FIN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00639 | hp2 | a0005 | c0015 | t0001 | g0066 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00735 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00738 | hp2 | a0003 | c0005 | t0001 | g0014 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01071 | hp2 | a0001 | c0010 | t0001 | g0005 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01099 | hp1 | a0006 | c0013 | t0001 | g0068 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0108 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01109 | hp1 | a0003 | c0005 | t0001 | g0014 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01175 | hp1 | a0003 | c0005 | t0001 | g0014 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0036 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01256 | hp1 | a0003 | c0005 | t0001 | g0041 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01258 | hp2 | a0003 | c0005 | t0001 | g0014 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01261 | hp1 | a0004 | c0008 | t0001 | g0010 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01433 | hp2 | a0005 | c0009 | t0001 | g0010 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01516 | hp1 | a0001 | c0011 | t0001 | g0004 | EUR | IBS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | IBS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01517 | hp2 | a0001 | c0011 | t0001 | g0004 | EUR | IBS | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0104 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02027 | hp1 | a0007 | c0021 | t0001 | g0001 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02040 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02071 | hp1 | a0008 | c0012 | t0001 | g0002 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02148 | hp1 | a0001 | c0010 | t0001 | g0005 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | CDX | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02165 | hp2 | a0001 | c0001 | t0006 | g0080 | EAS | CDX | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02257 | hp1 | a0001 | c0007 | t0002 | g0015 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02602 | hp2 | a0009 | c0022 | t0001 | g0001 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02622 | hp1 | a0004 | c0008 | t0001 | g0010 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02622 | hp2 | a0001 | c0007 | t0002 | g0015 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02630 | hp1 | a0004 | c0008 | t0001 | g0010 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02647 | hp2 | a0001 | c0006 | t0001 | g0012 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02818 | hp1 | a0001 | c0007 | t0002 | g0053 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0032 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02976 | hp2 | a0004 | c0023 | t0001 | g0040 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03486 | hp1 | a0001 | c0019 | t0001 | g0109 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0034 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0034 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | BEB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03927 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | BEB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0004 | SAS | STU | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | BEB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04199 | hp1 | a0001 | c0006 | t0001 | g0012 | SAS | STU | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | STU | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0004 | SAS | STU | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18522 | hp1 | a0010 | c0016 | t0001 | g0046 | AFR | YRI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18939 | hp2 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18943 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18948 | hp1 | a0001 | c0006 | t0003 | g0024 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18973 | hp2 | a0002 | c0014 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18980 | hp1 | a0001 | c0006 | t0003 | g0024 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18984 | hp1 | a0002 | c0004 | t0001 | g0064 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18986 | hp2 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18997 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19000 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19005 | hp2 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19011 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19030 | hp2 | a0011 | c0020 | t0001 | g0077 | AFR | LWK | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19043 | hp2 | a0001 | c0003 | t0001 | g0085 | AFR | LWK | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19059 | hp2 | a0002 | c0004 | t0001 | g0094 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19067 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19070 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19076 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19077 | hp1 | a0002 | c0004 | t0001 | g0084 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19240 | hp1 | a0012 | c0018 | t0001 | g0012 | AFR | YRI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ASW | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0004 | EUR | TSI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20805 | hp2 | a0001 | c0017 | t0007 | g0008 | EUR | TSI | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | GIH | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02109 | hp1 | a0005 | c0009 | t0001 | g0010 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | USA | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | USA | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | USA | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| homoSapiens | chm13v2 | a0013 | c0024 | t0001 | g0105 | REF | REF | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0002 | REF | REF | EIF4G1_chr3_184309606_184340353 | EIF4G1 | chr3 | 184309606 | 184340353 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:184321315 | G | A | 1 | a0008 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.731G>A | p.Arg244Gln | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/33 | 891/5405 | 731/4800 | 244/1599 | chr3 | 184321315 | |||
| chr3:184321516 | A | G | 1 | a0004 | 4 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(1): Show |
missense_variant | MODERATE | c.932A>G | p.Tyr311Cys | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/33 | 1092/5405 | 932/4800 | 311/1599 | chr3 | 184321516 | |||
| chr3:184321648 | C | T | 1 | a0009 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1064C>T | p.Thr355Ile | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/33 | 1224/5405 | 1064/4800 | 355/1599 | chr3 | 184321648 | |||
| chr3:184321878 | A | G | 9 | a0001 a0003 a0004 others(6): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
missense_variant | MODERATE | c.1294A>G | p.Met432Val | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/33 | 1454/5405 | 1294/4800 | 432/1599 | chr3 | 184321878 | |||
| chr3:184321915 | C | T | 1 | a0007 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1331C>T | p.Thr444Met | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/33 | 1491/5405 | 1331/4800 | 444/1599 | chr3 | 184321915 | |||
| chr3:184321978 | AAGGAGAA others(2): Show |
A | 1 | a0003 | 5 | HG00738.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.1413_1421delAGGAGA others(3): Show |
p.Gly472_Ala474del | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/33 | 1573/5405 | 1413/4800 | 471/1599 | INFO_REALIGN_3_PRIME | chr3 | 184321978 | ||
| chr3:184322583 | G | C | 1 | a0006 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1648G>C | p.Ala550Pro | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 12/33 | 1808/5405 | 1648/4800 | 550/1599 | chr3 | 184322583 | |||
| chr3:184323541 | C | T | 1 | a0011 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2222C>T | p.Thr741Met | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 15/33 | 2382/5405 | 2222/4800 | 741/1599 | chr3 | 184323541 | |||
| chr3:184327434 | G | A | 1 | a0010 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.3647G>A | p.Arg1216His | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 24/33 | 3807/5405 | 3647/4800 | 1216/1599 | chr3 | 184327434 | |||
| chr3:184327622 | T | C | 3 | a0003 a0004 a0005 |
12 | HG00639.hp2 HG00738.hp2 HG01109.hp1 others(9): Show |
missense_variant | MODERATE | c.3698T>C | p.Leu1233Pro | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 25/33 | 3858/5405 | 3698/4800 | 1233/1599 | chr3 | 184327622 | |||
| chr3:184327694 | A | G | 1 | a0012 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.3770A>G | p.Asn1257Ser | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 25/33 | 3930/5405 | 3770/4800 | 1257/1599 | chr3 | 184327694 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:184324221 | A | G | 1 | a0001c0019 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.2493A>G | p.Glu831Glu | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 17/33 | 2653/5405 | 2493/4800 | 831/1599 | chr3 | 184324221 | |||
| chr3:184324922 | G | A | 1 | a0005c0015 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.2664G>A | p.Arg888Arg | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 18/33 | 2824/5405 | 2664/4800 | 888/1599 | chr3 | 184324922 | |||
| chr3:184325325 | G | A | 1 | a0009c0022 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2913G>A | p.Thr971Thr | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 19/33 | 3073/5405 | 2913/4800 | 971/1599 | chr3 | 184325325 | |||
| chr3:184325494 | A | G | 1 | a0001c0011 | 2 | HG01516.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.2976A>G | p.Pro992Pro | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 20/33 | 3136/5405 | 2976/4800 | 992/1599 | chr3 | 184325494 | |||
| chr3:184325497 | C | T | 1 | a0004c0023 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2979C>T | p.Arg993Arg | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 20/33 | 3139/5405 | 2979/4800 | 993/1599 | chr3 | 184325497 | |||
| chr3:184327587 | G | C | 1 | a0002c0014 | 1 | NA18973.hp2 | splice_region_variant&synonymous_variant | LOW | c.3663G>C | p.Val1221Val | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 25/33 | 3823/5405 | 3663/4800 | 1221/1599 | chr3 | 184327587 | |||
| chr3:184328682 | C | T | 3 | a0001c0003 a0001c0011 a0001c0017 |
41 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(38): Show |
synonymous_variant | LOW | c.4005C>T | p.His1335His | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 27/33 | 4165/5405 | 4005/4800 | 1335/1599 | chr3 | 184328682 | |||
| chr3:184331355 | C | T | 1 | a0001c0006 | 4 | HG02647.hp2 HG04199.hp1 NA18948.hp1 others(1): Show |
synonymous_variant | LOW | c.4251C>T | p.Val1417Val | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 29/33 | 4411/5405 | 4251/4800 | 1417/1599 | chr3 | 184331355 | |||
| chr3:184331594 | C | T | 1 | a0001c0017 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.4383C>T | p.Phe1461Phe | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 30/33 | 4543/5405 | 4383/4800 | 1461/1599 | chr3 | 184331594 | |||
| chr3:184331597 | C | T | 1 | a0001c0010 | 2 | HG01071.hp2 HG02148.hp1 |
synonymous_variant | LOW | c.4386C>T | p.Asp1462Asp | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 30/33 | 4546/5405 | 4386/4800 | 1462/1599 | chr3 | 184331597 | |||
| chr3:184331796 | T | C | 1 | a0002c0004 | 8 | NA18939.hp2 NA18984.hp1 NA18986.hp2 others(5): Show |
synonymous_variant | LOW | c.4464T>C | p.Tyr1488Tyr | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 31/33 | 4624/5405 | 4464/4800 | 1488/1599 | chr3 | 184331796 | |||
| chr3:184331978 | C | T | 1 | a0001c0007 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
synonymous_variant | LOW | c.4510C>T | p.Leu1504Leu | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/33 | 4670/5405 | 4510/4800 | 1504/1599 | chr3 | 184331978 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:184314653 | C | G | 1 | a0001c0001t0008 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-113C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/33 | 1144 | chr3 | 184314653 | ||||||
| chr3:184314654 | G | C | 1 | a0001c0001t0008 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-112G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/33 | 1143 | chr3 | 184314654 | ||||||
| chr3:184314655 | C | T | 1 | a0001c0001t0008 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/33 | 1142 | chr3 | 184314655 | ||||||
| chr3:184314662 | A | G | 1 | a0001c0001t0008 | 1 | HG02040.hp2 | 5_prime_UTR_variant | MODIFIER | c.-104A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/33 | 1135 | chr3 | 184314662 | ||||||
| chr3:184335055 | A | T | 1 | a0001c0017t0007 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*147A>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 33/33 | 147 | chr3 | 184335055 | ||||||
| chr3:184335094 | C | T | 1 | a0001c0006t0003 | 2 | NA18948.hp1 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 33/33 | 186 | chr3 | 184335094 | ||||||
| chr3:184335229 | C | T | 1 | a0001c0001t0006 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 33/33 | 321 | chr3 | 184335229 | ||||||
| chr3:184335256 | G | T | 1 | a0001c0001t0005 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*348G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 33/33 | 348 | chr3 | 184335256 | ||||||
| chr3:184335311 | G | C | 1 | a0001c0007t0002 | 3 | HG02257.hp1 HG02622.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*403G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 33/33 | 403 | chr3 | 184335311 | ||||||
| chr3:184335349 | A | G | 1 | a0001c0001t0004 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*441A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 33/33 | 441 | chr3 | 184335349 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:184314712 | AC | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0003t0001g0036 |
4 | HG00140.hp1 HG01243.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92+43delC | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr3 | 184314712 | ||||||
| chr3:184314715 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-92+41C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184314715 | |||||||
| chr3:184314821 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0114 |
4 | HG01167.hp1 HG01169.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92+147C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184314821 | |||||||
| chr3:184314850 | C | T | 1 | a0002c0002t0001g0035 | 2 | NA18993.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-92+176C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184314850 | |||||||
| chr3:184314912 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92+238G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184314912 | |||||||
| chr3:184315025 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-92+351C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315025 | |||||||
| chr3:184315094 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0112 |
6 | NA18974.hp1 NA18988.hp2 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.-91-395C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315094 | |||||||
| chr3:184315123 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-91-366A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315123 | |||||||
| chr3:184315134 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-91-355C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315134 | |||||||
| chr3:184315285 | G | C | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-91-204G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315285 | |||||||
| chr3:184315294 | C | T | 2 | a0001c0003t0001g0008 a0001c0017t0007g0008 |
9 | HG01496.hp1 HG02698.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-91-195C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315294 | |||||||
| chr3:184315300 | G | A | 1 | a0001c0006t0003g0024 | 2 | NA18948.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-91-189G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315300 | |||||||
| chr3:184315424 | A | C | 1 | a0001c0019t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-91-65A>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 1/32 | chr3 | 184315424 | |||||||
| chr3:184315558 | T | A | 6 | a0001c0001t0001g0039 a0003c0005t0001g0014 a0003c0005t0001g0041 others(3): Show |
12 | HG00738.hp2 HG01109.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-35+13T>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 2/32 | chr3 | 184315558 | |||||||
| chr3:184315620 | A | T | 9 | a0001c0003t0001g0004 a0001c0003t0001g0008 a0001c0003t0001g0034 others(6): Show |
36 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-35+75A>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 2/32 | chr3 | 184315620 | |||||||
| chr3:184315869 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.60+13G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 3/32 | chr3 | 184315869 | |||||||
| chr3:184315876 | CAGG | C | 2 | a0003c0005t0001g0014 a0003c0005t0001g0041 |
5 | HG00738.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.60+21_60+23delAGG | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 3/32 | chr3 | 184315876 | |||||||
| chr3:184316333 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA18941.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.147+115G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 4/32 | chr3 | 184316333 | |||||||
| chr3:184316552 | GT | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0010c0016t0001g0046 |
3 | HG03209.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.147+335delT | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 4/32 | chr3 | 184316552 | |||||||
| chr3:184316586 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.147+368T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 4/32 | chr3 | 184316586 | |||||||
| chr3:184316598 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.147+380C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 4/32 | chr3 | 184316598 | |||||||
| chr3:184316846 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.148-475G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 4/32 | chr3 | 184316846 | |||||||
| chr3:184316948 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.148-373C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 4/32 | chr3 | 184316948 | |||||||
| chr3:184317604 | T | A | 4 | a0001c0001t0001g0039 a0004c0008t0001g0010 a0004c0023t0001g0040 others(1): Show |
7 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+107T>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 5/32 | chr3 | 184317604 | |||||||
| chr3:184317660 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0010c0016t0001g0046 |
3 | HG03209.hp1 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.325-57G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 5/32 | chr3 | 184317660 | |||||||
| chr3:184317950 | G | A | 1 | a0001c0001t0001g0023 | 3 | HG01167.hp1 HG01169.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.424+134G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184317950 | |||||||
| chr3:184318072 | A | G | 2 | a0003c0005t0001g0014 a0003c0005t0001g0041 |
5 | HG00738.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+256A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318072 | |||||||
| chr3:184318129 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.424+313T>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318129 | |||||||
| chr3:184318198 | G | C | 1 | a0001c0001t0001g0049 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.424+382G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318198 | |||||||
| chr3:184318220 | C | G | 4 | a0001c0001t0001g0039 a0004c0008t0001g0010 a0004c0023t0001g0040 others(1): Show |
7 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+404C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318220 | |||||||
| chr3:184318226 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.424+410G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318226 | |||||||
| chr3:184318549 | C | T | 4 | a0001c0001t0001g0039 a0004c0008t0001g0010 a0004c0023t0001g0040 others(1): Show |
7 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+733C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318549 | |||||||
| chr3:184318570 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.424+754A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318570 | |||||||
| chr3:184318596 | T | C | 1 | a0001c0003t0001g0104 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.424+780T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318596 | |||||||
| chr3:184318824 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.425-865C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318824 | |||||||
| chr3:184318825 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.425-864G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318825 | |||||||
| chr3:184318907 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.425-782G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318907 | |||||||
| chr3:184318936 | T | C | 2 | a0001c0001t0001g0045 a0010c0016t0001g0046 |
2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.425-753T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318936 | |||||||
| chr3:184318948 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.425-741C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318948 | |||||||
| chr3:184318988 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG02615.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.425-701C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318988 | |||||||
| chr3:184318998 | C | T | 1 | a0002c0002t0001g0098 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.425-691C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184318998 | |||||||
| chr3:184319073 | C | CA | 9 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0054 others(6): Show |
13 | HG00639.hp1 HG00738.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.425-601dupA | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319073 | ||||||
| chr3:184319073 | CA | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
8 | HG02976.hp2 NA18954.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-601delA | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319073 | ||||||
| chr3:184319106 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
121 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.425-583C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319106 | |||||||
| chr3:184319425 | GGGTGTGT others(4): Show |
G | 1 | a0001c0001t0001g0091 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.425-262_425-252del others(11): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319425 | ||||||
| chr3:184319425 | GGGTGTGT others(8): Show |
G | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.425-262_425-248del others(15): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319425 | ||||||
| chr3:184319425 | GGGTGTGT others(10): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.425-262_425-246del others(17): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319425 | ||||||
| chr3:184319426 | G | GGT | 3 | a0002c0002t0001g0002 a0002c0004t0001g0064 a0006c0013t0001g0068 |
5 | HG01099.hp1 HG01099.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.425-224_425-223dup others(2): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319426 | ||||||
| chr3:184319426 | G | GGTGT | 5 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0058 others(2): Show |
5 | HG00609.hp1 HG02132.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.425-226_425-223dup others(4): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319426 | ||||||
| chr3:184319426 | G | T | 1 | a0002c0002t0001g0006 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.425-263G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319426 | |||||||
| chr3:184319426 | GGT | G | 4 | a0001c0001t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0006 others(1): Show |
13 | HG00597.hp2 HG00642.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.425-224_425-223del others(2): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319426 | ||||||
| chr3:184319426 | GGTGT | G | 6 | a0001c0001t0001g0011 a0002c0002t0001g0002 a0002c0002t0001g0006 others(3): Show |
12 | HG00544.hp2 HG02523.hp2 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-226_425-223del others(4): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319426 | ||||||
| chr3:184319426 | GGTGTGTG others(35): Show |
G | 1 | a0005c0009t0001g0010 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.425-246_425-205del others(42): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319426 | ||||||
| chr3:184319428 | T | G | 2 | a0001c0001t0001g0001 a0001c0011t0001g0004 |
3 | HG01516.hp1 HG01517.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.425-261T>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319428 | |||||||
| chr3:184319431 | GTGTGTGT others(29): Show |
G | 1 | a0001c0003t0001g0032 | 2 | HG02615.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.425-240_425-205del others(36): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319431 | ||||||
| chr3:184319439 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0001g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.425-232_425-205del others(28): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319439 | ||||||
| chr3:184319445 | GTGTGTGT others(15): Show |
G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0001t0001g0078 |
3 | HG02451.hp2 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.425-226_425-205del others(22): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319445 | ||||||
| chr3:184319447 | G | T | 1 | a0001c0001t0001g0001 | 2 | HG00597.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.425-242G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319447 | |||||||
| chr3:184319447 | GTGTGTGT others(13): Show |
G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0039 others(5): Show |
11 | HG02080.hp2 HG02129.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.425-224_425-205del others(20): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319447 | ||||||
| chr3:184319449 | GTGTGTGT others(11): Show |
G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0020 others(11): Show |
17 | HG00738.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.425-221_425-204del others(18): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319449 | ||||||
| chr3:184319451 | GTGTGTGT others(9): Show |
G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(30): Show |
67 | HG00099.hp1 HG00323.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.425-222_425-207del others(16): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319451 | ||||||
| chr3:184319453 | GTGTGTGT others(7): Show |
G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(24): Show |
60 | HG00423.hp1 HG00609.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.425-222_425-209del others(14): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319453 | ||||||
| chr3:184319455 | GTGTGTGT others(5): Show |
G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(28): Show |
71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.425-222_425-211del others(12): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319455 | ||||||
| chr3:184319457 | GTGTGTGT others(3): Show |
G | 16 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(13): Show |
29 | HG00099.hp2 HG00438.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.425-222_425-213del others(10): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319457 | ||||||
| chr3:184319459 | G | T | 2 | a0002c0002t0001g0002 a0002c0002t0001g0093 |
2 | NA18994.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.425-230G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319459 | |||||||
| chr3:184319459 | GTGTGTGT others(1): Show |
G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(7): Show |
21 | HG00558.hp2 HG01952.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.425-222_425-215del others(8): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319459 | ||||||
| chr3:184319461 | GTGTGTT | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0005g0095 others(1): Show |
5 | HG02027.hp2 HG02135.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-222_425-217del others(6): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | INFO_REALIGN_3_PRIME | chr3 | 184319461 | ||||||
| chr3:184319467 | T | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0071 others(5): Show |
9 | HG00544.hp1 HG01891.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-222T>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319467 | |||||||
| chr3:184319646 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.425-43C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319646 | |||||||
| chr3:184319677 | C | T | 1 | a0002c0004t0001g0084 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.425-12C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319677 | |||||||
| chr3:184319679 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.425-10C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 6/32 | chr3 | 184319679 | |||||||
| chr3:184319928 | T | G | 7 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0045 others(4): Show |
7 | HG02451.hp2 HG03098.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.537+127T>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 7/32 | chr3 | 184319928 | |||||||
| chr3:184319980 | G | A | 1 | a0001c0019t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.537+179G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 7/32 | chr3 | 184319980 | |||||||
| chr3:184320012 | G | GGAAGTTC others(11): Show |
1 | a0001c0001t0005g0095 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.537+213_537+230dup others(18): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 7/32 | INFO_REALIGN_3_PRIME | chr3 | 184320012 | ||||||
| chr3:184320288 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.538-342C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 7/32 | chr3 | 184320288 | |||||||
| chr3:184320343 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.538-287G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 7/32 | chr3 | 184320343 | |||||||
| chr3:184320738 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.630+16C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 8/32 | chr3 | 184320738 | |||||||
| chr3:184321043 | A | G | 1 | a0002c0002t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.697+50A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 9/32 | chr3 | 184321043 | |||||||
| chr3:184321086 | A | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(53): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.697+93A>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 9/32 | chr3 | 184321086 | |||||||
| chr3:184321181 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(19): Show |
74 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.698-101C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 9/32 | chr3 | 184321181 | |||||||
| chr3:184321240 | G | A | 1 | a0001c0001t0001g0021 | 3 | NA18960.hp2 NA18963.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.698-42G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 9/32 | chr3 | 184321240 | |||||||
| chr3:184322147 | A | G | 1 | a0010c0016t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1519+44A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/32 | chr3 | 184322147 | |||||||
| chr3:184322149 | C | G | 3 | a0004c0008t0001g0010 a0004c0023t0001g0040 a0005c0009t0001g0010 |
6 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1519+46C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/32 | chr3 | 184322149 | |||||||
| chr3:184322229 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1519+126G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/32 | chr3 | 184322229 | |||||||
| chr3:184322321 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1520-41T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/32 | chr3 | 184322321 | |||||||
| chr3:184322340 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1520-22T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 10/32 | chr3 | 184322340 | |||||||
| chr3:184322739 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1795+9A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 12/32 | chr3 | 184322739 | |||||||
| chr3:184322756 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG02559.hp2 HG02970.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1795+26G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 12/32 | chr3 | 184322756 | |||||||
| chr3:184322818 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.1796-3C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 12/32 | chr3 | 184322818 | |||||||
| chr3:184323356 | A | G | 1 | a0001c0003t0001g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2089-52A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 14/32 | chr3 | 184323356 | |||||||
| chr3:184323610 | C | T | 1 | a0002c0002t0001g0027 | 2 | HG02015.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.2274+17C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 15/32 | chr3 | 184323610 | |||||||
| chr3:184323650 | G | A | 1 | a0001c0001t0001g0021 | 3 | NA18960.hp2 NA18963.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2274+57G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 15/32 | chr3 | 184323650 | |||||||
| chr3:184323711 | C | G | 3 | a0004c0008t0001g0010 a0004c0023t0001g0040 a0005c0009t0001g0010 |
6 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2275-69C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 15/32 | chr3 | 184323711 | |||||||
| chr3:184324119 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG02257.hp2 HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2473-82C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 16/32 | chr3 | 184324119 | |||||||
| chr3:184324183 | A | G | 3 | a0004c0008t0001g0010 a0004c0023t0001g0040 a0005c0009t0001g0010 |
6 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2473-18A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 16/32 | chr3 | 184324183 | |||||||
| chr3:184324527 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2619+180G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 17/32 | chr3 | 184324527 | |||||||
| chr3:184324742 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2620-136G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 17/32 | chr3 | 184324742 | |||||||
| chr3:184324856 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2620-22A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 17/32 | chr3 | 184324856 | |||||||
| chr3:184325214 | G | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0055 a0001c0001t0006g0080 |
4 | HG00639.hp1 HG02040.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.2857-55G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 18/32 | chr3 | 184325214 | |||||||
| chr3:184325231 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2857-38A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 18/32 | chr3 | 184325231 | |||||||
| chr3:184325427 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0071 |
8 | HG01891.hp1 HG02109.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2962-53T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 19/32 | chr3 | 184325427 | |||||||
| chr3:184325848 | C | T | 1 | a0001c0001t0001g0016 | 4 | HG02559.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3122-3C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 20/32 | chr3 | 184325848 | |||||||
| chr3:184326137 | A | AAC | 15 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(12): Show |
29 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.3222+217_3222+218d others(4): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326137 | ||||||
| chr3:184326137 | A | AACAC | 3 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0100 |
6 | HG02559.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3222+215_3222+218d others(6): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326137 | ||||||
| chr3:184326137 | A | AACACAC | 3 | a0001c0001t0001g0003 a0001c0001t0001g0037 a0001c0001t0001g0099 |
3 | HG03195.hp1 HG03209.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.3222+213_3222+218d others(8): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326137 | ||||||
| chr3:184326137 | A | AACACACA others(3): Show |
1 | a0001c0001t0001g0045 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3222+209_3222+218d others(12): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326137 | ||||||
| chr3:184326137 | AAC | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(42): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.3222+217_3222+218d others(4): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326137 | ||||||
| chr3:184326137 | AACAC | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0087 others(2): Show |
5 | HG02451.hp2 HG06807.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.3222+215_3222+218d others(6): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326137 | ||||||
| chr3:184326137 | AACACACA others(3): Show |
A | 1 | a0005c0015t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3222+209_3222+218d others(12): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326137 | ||||||
| chr3:184326225 | T | TA | 3 | a0004c0008t0001g0010 a0004c0023t0001g0040 a0005c0009t0001g0010 |
6 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.3222+277dupA | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | INFO_REALIGN_3_PRIME | chr3 | 184326225 | ||||||
| chr3:184326460 | A | G | 1 | a0006c0013t0001g0068 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3223-67A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 21/32 | chr3 | 184326460 | |||||||
| chr3:184326645 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0111 others(1): Show |
21 | HG00733.hp1 HG01071.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.3325+16C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 22/32 | chr3 | 184326645 | |||||||
| chr3:184326734 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0099 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3325+105C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 22/32 | chr3 | 184326734 | |||||||
| chr3:184327130 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3429-86G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 23/32 | chr3 | 184327130 | |||||||
| chr3:184327569 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3662-17G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 24/32 | chr3 | 184327569 | |||||||
| chr3:184327774 | C | T | 1 | a0001c0003t0001g0108 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3781-56C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 25/32 | chr3 | 184327774 | |||||||
| chr3:184328011 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(105): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.3953+9A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328011 | |||||||
| chr3:184328034 | T | C | 1 | a0005c0015t0001g0066 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3953+32T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328034 | |||||||
| chr3:184328051 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3953+49C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328051 | |||||||
| chr3:184328178 | C | T | 1 | a0001c0003t0001g0034 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3953+176C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328178 | |||||||
| chr3:184328254 | A | G | 27 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(24): Show |
89 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.3953+252A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328254 | |||||||
| chr3:184328289 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3953+287G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328289 | |||||||
| chr3:184328303 | A | G | 2 | a0001c0003t0001g0032 a0001c0003t0001g0085 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3953+301A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328303 | |||||||
| chr3:184328314 | C | G | 10 | a0001c0003t0001g0004 a0001c0003t0001g0008 a0001c0003t0001g0034 others(7): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.3953+312C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328314 | |||||||
| chr3:184328339 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3954-292C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328339 | |||||||
| chr3:184328402 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3954-229A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328402 | |||||||
| chr3:184328408 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3954-223C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328408 | |||||||
| chr3:184328448 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3954-183G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328448 | |||||||
| chr3:184328459 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3954-172G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328459 | |||||||
| chr3:184328567 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.3954-64C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328567 | |||||||
| chr3:184328621 | C | T | 1 | a0010c0016t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3954-10C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 26/32 | chr3 | 184328621 | |||||||
| chr3:184328770 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0099 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4079+14G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 27/32 | chr3 | 184328770 | |||||||
| chr3:184329016 | A | T | 1 | a0002c0004t0001g0094 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.4161+26A>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329016 | |||||||
| chr3:184329131 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0090 |
4 | HG02145.hp1 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4161+141C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329131 | |||||||
| chr3:184329346 | A | T | 2 | a0003c0005t0001g0014 a0003c0005t0001g0041 |
5 | HG00738.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.4161+356A>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329346 | |||||||
| chr3:184329358 | C | T | 3 | a0004c0008t0001g0010 a0004c0023t0001g0040 a0005c0009t0001g0010 |
6 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.4161+368C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329358 | |||||||
| chr3:184329391 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0072 |
3 | HG01257.hp1 HG01258.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.4161+401G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329391 | |||||||
| chr3:184329438 | T | C | 3 | a0004c0008t0001g0010 a0004c0023t0001g0040 a0005c0009t0001g0010 |
6 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.4161+448T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329438 | |||||||
| chr3:184329484 | A | G | 1 | a0002c0002t0001g0026 | 2 | NA18982.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.4161+494A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329484 | |||||||
| chr3:184329522 | AGGAGGCT others(24): Show |
A | 1 | a0001c0001t0001g0073 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4161+539_4161+569d others(33): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr3 | 184329522 | ||||||
| chr3:184329566 | A | G | 10 | a0001c0003t0001g0004 a0001c0003t0001g0008 a0001c0003t0001g0034 others(7): Show |
38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.4161+576A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329566 | |||||||
| chr3:184329778 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0099 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4161+788C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329778 | |||||||
| chr3:184329872 | T | G | 1 | a0001c0001t0001g0073 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4161+882T>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184329872 | |||||||
| chr3:184330048 | A | C | 1 | a0001c0003t0001g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4161+1058A>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330048 | |||||||
| chr3:184330142 | A | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(68): Show |
177 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.4162-1124A>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330142 | |||||||
| chr3:184330188 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0048 others(1): Show |
14 | HG01257.hp2 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.4162-1078C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330188 | |||||||
| chr3:184330309 | G | C | 2 | a0003c0005t0001g0014 a0003c0005t0001g0041 |
5 | HG00738.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.4162-957G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330309 | |||||||
| chr3:184330344 | A | C | 1 | a0011c0020t0001g0077 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4162-922A>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330344 | |||||||
| chr3:184330357 | C | T | 1 | a0001c0019t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4162-909C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330357 | |||||||
| chr3:184330405 | G | C | 2 | a0001c0003t0001g0032 a0001c0003t0001g0085 |
3 | HG02615.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4162-861G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330405 | |||||||
| chr3:184330417 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4162-849T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330417 | |||||||
| chr3:184330429 | T | C | 1 | a0001c0001t0001g0016 | 4 | HG02559.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4162-837T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330429 | |||||||
| chr3:184330646 | CT | C | 3 | a0001c0001t0001g0015 a0001c0007t0002g0015 a0001c0007t0002g0053 |
5 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.4162-618delT | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr3 | 184330646 | ||||||
| chr3:184330654 | A | G | 1 | a0001c0001t0006g0080 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4162-612A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330654 | |||||||
| chr3:184330678 | T | TA | 1 | a0001c0001t0001g0016 | 4 | HG02559.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4162-587dupA | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr3 | 184330678 | ||||||
| chr3:184330690 | C | T | 1 | a0001c0001t0001g0016 | 4 | HG02559.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.4162-576C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330690 | |||||||
| chr3:184330810 | C | T | 1 | a0001c0019t0001g0109 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4162-456C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330810 | |||||||
| chr3:184330830 | C | T | 1 | a0001c0003t0001g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4162-436C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330830 | |||||||
| chr3:184330880 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0076 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.4162-386C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184330880 | |||||||
| chr3:184331071 | TTGAC | T | 2 | a0003c0005t0001g0014 a0003c0005t0001g0041 |
5 | HG00738.hp2 HG01109.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.4162-190_4162-187d others(6): Show |
EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | INFO_REALIGN_3_PRIME | chr3 | 184331071 | ||||||
| chr3:184331183 | A | G | 2 | a0001c0001t0001g0020 a0011c0020t0001g0077 |
4 | HG00735.hp1 HG02572.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4162-83A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 28/32 | chr3 | 184331183 | |||||||
| chr3:184331428 | T | C | 1 | a0002c0002t0001g0067 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.4261-44T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 29/32 | chr3 | 184331428 | |||||||
| chr3:184331611 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0099 a0010c0016t0001g0046 |
3 | HG03195.hp1 HG03540.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.4395+5G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 30/32 | chr3 | 184331611 | |||||||
| chr3:184331708 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0007t0002g0015 others(1): Show |
6 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4396-20C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 30/32 | chr3 | 184331708 | |||||||
| chr3:184332172 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4618+86C>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184332172 | |||||||
| chr3:184332539 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4618+453G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184332539 | |||||||
| chr3:184332560 | G | C | 1 | a0002c0002t0001g0060 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.4618+474G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184332560 | |||||||
| chr3:184332992 | T | C | 1 | a0002c0002t0001g0061 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4618+906T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184332992 | |||||||
| chr3:184333074 | A | G | 1 | a0002c0004t0001g0064 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4618+988A>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333074 | |||||||
| chr3:184333178 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4618+1092G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333178 | |||||||
| chr3:184333391 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4618+1305C>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333391 | |||||||
| chr3:184333527 | A | C | 1 | a0001c0001t0001g0054 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.4619-1200A>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333527 | |||||||
| chr3:184333579 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0099 |
2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4619-1148G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333579 | |||||||
| chr3:184333839 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA18960.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4619-888G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333839 | |||||||
| chr3:184333858 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0022 others(13): Show |
31 | HG00639.hp1 HG00733.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.4619-869G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333858 | |||||||
| chr3:184333937 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4619-790G>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184333937 | |||||||
| chr3:184334087 | C | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(56): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.4619-640C>G | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334087 | |||||||
| chr3:184334263 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4619-464G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334263 | |||||||
| chr3:184334286 | G | A | 1 | a0002c0002t0001g0061 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4619-441G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334286 | |||||||
| chr3:184334345 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4619-382G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334345 | |||||||
| chr3:184334401 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG00733.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.4619-326T>C | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334401 | |||||||
| chr3:184334546 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0048 others(2): Show |
15 | HG01257.hp2 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.4619-181G>A | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334546 | |||||||
| chr3:184334632 | G | T | 1 | a0001c0001t0001g0019 | 3 | HG00099.hp2 HG00323.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4619-95G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334632 | |||||||
| chr3:184334687 | G | T | 1 | a0002c0002t0001g0063 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4619-40G>T | EIF4G1 | ENSG00000114867.22 | transcript | ENST00000346169.7 | protein_coding | 32/32 | chr3 | 184334687 |