Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1939 |
| ensemblid | ENSG00000143486.16 |
| hgncid | 6583 |
| symbol | EIF2D |
| name | eukaryotic translation initiation factor 2D |
| refseq_nuc | NM_006893.3 |
| refseq_prot | NP_008824.2 |
| ensembl_nuc | ENST00000271764.7 |
| ensembl_prot | ENSP00000271764.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 206591642 |
| end | 206612465 |
| strand | - |
| ver | v1.2 |
| region | chr1:206591642-206612465 |
| region5000 | chr1:206586642-206617465 |
| regionname0 | EIF2D_chr1_206591642_206612465 |
| regionname5000 | EIF2D_chr1_206586642_206617465 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 584 | 402 | 75 | 67 | 210 | 12 | 36 | 166 | EIF2D_chr1_206586642_206617465 | EIF2D | MFAKA others(579): Show |
chr1 | 206586642 | 206617465 |
| a0002 | 0/0 | 584 | 23 | 20 | 1 | 0 | 0 | 2 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | MFAKA others(579): Show |
chr1 | 206586642 | 206617465 |
| a0003 | 0/0 | 584 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | MFAKA others(579): Show |
chr1 | 206586642 | 206617465 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1752 | 395 | 71 | 67 | 208 | 12 | 35 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 | ||
| a0001c0003 | 0/0 | 1752 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 | ||
| a0001c0004 | 0/0 | 1752 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 | ||
| a0001c0005 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 | ||
| a0001c0006 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 | ||
| a0001c0007 | 0/0 | 1752 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 | ||
| a0002c0002 | 0/0 | 1752 | 23 | 20 | 1 | 0 | 0 | 2 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 | ||
| a0003c0008 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | ATGTT others(1747): Show |
chr1 | 206586642 | 206617465 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2011 | 392 | 71 | 65 | 207 | 12 | 35 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0001c0001t0002 | 0/0 | 2011 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0001c0001t0003 | 0/0 | 2011 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | TCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0001c0003t0001 | 0/0 | 2011 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0001c0004t0001 | 0/0 | 2011 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0001c0005t0001 | 0/0 | 2011 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0001c0006t0001 | 0/0 | 2011 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0001c0007t0001 | 0/0 | 2011 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0002c0002t0001 | 0/0 | 2011 | 23 | 20 | 1 | 0 | 0 | 2 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| a0003c0008t0001 | 0/0 | 2011 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | CCTTT others(2006): Show |
chr1 | 206586642 | 206617465 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 34 | 3 | 1 | 24 | 0 | 6 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0002 | 0/0 | 29 | 0 | 9 | 17 | 0 | 3 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0003 | 0/0 | 19 | 0 | 9 | 10 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0004 | 0/0 | 14 | 0 | 2 | 9 | 3 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0005 | 0/0 | 13 | 3 | 1 | 8 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0007 | 0/0 | 8 | 5 | 2 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0009 | 1/1 | 7 | 1 | 0 | 3 | 1 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0010 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0014 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0018 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0027 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0029 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0005t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0001c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| a0003c0008t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00423 | hp1 | a0001 | c0007 | t0001 | g0163 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CDX | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0070 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0134 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0115 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0186 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0203 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0061 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | YRI | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19086 | hp1 | a0001 | c0006 | t0001 | g0123 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | YRI | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ASW | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | GIH | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02559 | hp1 | a0003 | c0008 | t0001 | g0140 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0133 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | USA | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0009 | REF | REF | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | EIF2D_chr1_206586642_206617465 | EIF2D | chr1 | 206586642 | 206617465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:206603106 | G | A | 1 | a0002 | 23 | HG01257.hp1 HG01891.hp1 HG02055.hp2 others(20): Show |
missense_variant | MODERATE | c.629C>T | p.Thr210Ile | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/15 | 752/2011 | 629/1755 | 210/584 | chr1 | 206603106 | |||
| chr1:206608281 | T | A | 1 | a0003 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.377A>T | p.Gln126Leu | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/15 | 500/2011 | 377/1755 | 126/584 | chr1 | 206608281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:206593653 | T | C | 1 | a0001c0006 | 1 | NA19086.hp1 | synonymous_variant | LOW | c.1650A>G | p.Gly550Gly | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/15 | 1773/2011 | 1650/1755 | 550/584 | chr1 | 206593653 | |||
| chr1:206595796 | G | A | 1 | a0001c0007 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.1431C>T | p.Pro477Pro | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/15 | 1554/2011 | 1431/1755 | 477/584 | chr1 | 206595796 | |||
| chr1:206599089 | C | T | 1 | a0001c0005 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1206G>A | p.Lys402Lys | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/15 | 1329/2011 | 1206/1755 | 402/584 | chr1 | 206599089 | |||
| chr1:206603126 | C | T | 1 | a0001c0003 | 3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
synonymous_variant | LOW | c.609G>A | p.Gly203Gly | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/15 | 732/2011 | 609/1755 | 203/584 | chr1 | 206603126 | |||
| chr1:206611257 | C | T | 1 | a0001c0004 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.174G>A | p.Gly58Gly | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/15 | 297/2011 | 174/1755 | 58/584 | chr1 | 206611257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:206591751 | C | T | 1 | a0001c0001t0002 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*24G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 15/15 | 24 | chr1 | 206591751 | ||||||
| chr1:206612465 | G | A | 1 | a0001c0001t0003 | 1 | NA19010.hp2 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/15 | 123 | chr1 | 206612465 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:206591922 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(13): Show |
41 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1685-77G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206591922 | |||||||
| chr1:206592146 | T | C | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1685-301A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592146 | |||||||
| chr1:206592339 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0002g0051 |
3 | HG01069.hp1 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1685-494G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592339 | |||||||
| chr1:206592340 | G | A | 18 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(15): Show |
43 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1685-495C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592340 | |||||||
| chr1:206592460 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0144 |
3 | HG02071.hp2 NA18950.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1685-615G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592460 | |||||||
| chr1:206592467 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1685-622C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592467 | |||||||
| chr1:206592574 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1685-729C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592574 | |||||||
| chr1:206592669 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1685-824A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592669 | |||||||
| chr1:206592939 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0063 |
3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1684+680A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206592939 | |||||||
| chr1:206593110 | C | CA | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(114): Show |
212 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1684+508dupT | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593110 | |||||||
| chr1:206593110 | C | CAA | 3 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0100 |
8 | HG01884.hp2 HG02258.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1684+507_1684+508d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593110 | |||||||
| chr1:206593162 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
210 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1684+457T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593162 | |||||||
| chr1:206593466 | G | GGA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0110 others(5): Show |
14 | HG00280.hp2 HG00642.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1684+151_1684+152d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593466 | |||||||
| chr1:206593466 | G | GGAGA | 8 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG01123.hp1 HG02132.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1684+149_1684+152d others(6): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593466 | |||||||
| chr1:206593484 | A | AGAGAGAG others(5): Show |
1 | a0001c0003t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1684+134_1684+135i others(14): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593484 | |||||||
| chr1:206593486 | A | AGAGAGC | 3 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0002c0002t0001g0206 |
4 | HG01261.hp2 HG02698.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1684+132_1684+133i others(8): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593486 | |||||||
| chr1:206593486 | A | AGAGC | 53 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(50): Show |
114 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.1684+132_1684+133i others(6): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593486 | |||||||
| chr1:206593486 | A | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0018 others(39): Show |
73 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.1684+133T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593486 | |||||||
| chr1:206593488 | C | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0185 a0001c0001t0001g0199 others(1): Show |
4 | HG02717.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1684+131G>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593488 | |||||||
| chr1:206593488 | C | CGAGA | 11 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0053 others(8): Show |
31 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1684+127_1684+130d others(6): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593488 | |||||||
| chr1:206593490 | A | C | 12 | a0001c0001t0001g0044 a0001c0001t0001g0152 a0001c0001t0001g0153 others(9): Show |
14 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1684+129T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593490 | |||||||
| chr1:206593492 | A | C | 1 | a0001c0001t0002g0051 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1684+127T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593492 | |||||||
| chr1:206593506 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0155 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1684+112_1684+113i others(16): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593506 | A | AGTGTGTG others(3): Show |
33 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(30): Show |
77 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1684+112_1684+113i others(12): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593506 | A | AGTGTGTG others(5): Show |
6 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0036 others(3): Show |
13 | HG01516.hp1 HG01517.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1684+112_1684+113i others(14): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593506 | A | AGTGTGTG others(7): Show |
10 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0117 others(7): Show |
17 | HG01358.hp2 HG02083.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1684+112_1684+113i others(16): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593506 | A | AGTGTGTG others(9): Show |
12 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0029 others(9): Show |
26 | HG00408.hp1 HG00735.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.1684+112_1684+113i others(18): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593506 | A | AGTGTGTG others(11): Show |
21 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0060 others(18): Show |
37 | HG00140.hp1 HG00423.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1684+112_1684+113i others(20): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593506 | A | AGTGTGTG others(13): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0001g0136 |
6 | HG01361.hp2 HG02300.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1684+112_1684+113i others(22): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593506 | A | AGTGTGTG others(15): Show |
2 | a0001c0001t0001g0120 a0001c0001t0001g0151 |
2 | NA18940.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1684+112_1684+113i others(24): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593506 | |||||||
| chr1:206593508 | A | AGAGAGAG others(15): Show |
1 | a0001c0003t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1684+110_1684+111i others(24): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGAGAGAG others(21): Show |
1 | a0001c0003t0001g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1684+110_1684+111i others(30): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGAGAGTG others(3): Show |
1 | a0001c0001t0001g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1684+110_1684+111i others(12): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGAGAGTG others(7): Show |
1 | a0001c0001t0001g0030 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1684+110_1684+111i others(16): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGAGAGTG others(13): Show |
1 | a0001c0001t0001g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1684+110_1684+111i others(22): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGAGTGT | 2 | a0001c0001t0001g0024 a0001c0001t0001g0033 |
5 | NA18950.hp2 NA18952.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1684+110_1684+111i others(8): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGAGTGTG others(3): Show |
2 | a0001c0001t0001g0192 a0001c0001t0001g0208 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1684+110_1684+111i others(12): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGAGTGTG others(13): Show |
1 | a0001c0001t0002g0051 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1684+110_1684+111i others(22): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0041 a0001c0001t0001g0075 others(5): Show |
27 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.1684+109_1684+110d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGT | 6 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0042 others(3): Show |
10 | HG01109.hp2 HG02109.hp2 NA18522.hp1 others(7): Show |
intron_variant | MODIFIER | c.1684+107_1684+110d others(6): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(11): Show |
1 | a0001c0001t0001g0154 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1684+110_1684+111i others(20): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(3): Show |
7 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG00741.hp2 HG03098.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1684+101_1684+110d others(12): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(5): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0093 a0001c0001t0001g0139 |
7 | HG00280.hp2 HG00642.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1684+110_1684+111i others(14): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(7): Show |
3 | a0001c0001t0001g0039 a0001c0001t0001g0091 a0001c0001t0001g0188 |
4 | HG01993.hp2 HG02886.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1684+110_1684+111i others(16): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(9): Show |
1 | a0001c0001t0001g0102 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1684+110_1684+111i others(18): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(13): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0153 a0001c0001t0001g0160 |
4 | HG00673.hp1 HG02074.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1684+110_1684+111i others(22): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(15): Show |
6 | a0001c0001t0001g0152 a0001c0001t0001g0175 a0002c0002t0001g0055 others(3): Show |
6 | HG00673.hp2 HG02723.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1684+110_1684+111i others(24): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(17): Show |
1 | a0002c0002t0001g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1684+110_1684+111i others(26): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0128 a0001c0001t0001g0164 |
2 | HG02132.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1684+99_1684+110du others(13): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1684+97_1684+110du others(15): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(9): Show |
1 | a0001c0001t0001g0028 | 3 | HG01081.hp1 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1684+95_1684+110du others(17): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(11): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1684+93_1684+110du others(19): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(13): Show |
1 | a0001c0001t0001g0141 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1684+91_1684+110du others(21): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | AGTGTGTG others(17): Show |
1 | a0001c0001t0001g0170 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1684+87_1684+110du others(25): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(30): Show |
77 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1684+111T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | A | T | 57 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0018 others(54): Show |
104 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1684+111T>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | AGT | A | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00099.hp1 HG00609.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1684+109_1684+110d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593508 | AGTGTGTG others(17): Show |
A | 1 | a0001c0001t0001g0082 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1684+87_1684+110de others(25): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593508 | |||||||
| chr1:206593510 | T | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0064 others(5): Show |
12 | HG02257.hp2 HG02630.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1684+109A>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593510 | |||||||
| chr1:206593512 | T | A | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG00099.hp1 HG00609.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.1684+107A>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593512 | |||||||
| chr1:206593514 | T | A | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00099.hp1 HG00609.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1684+105A>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 14/14 | chr1 | 206593514 | |||||||
| chr1:206593899 | T | C | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510-106A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206593899 | |||||||
| chr1:206594065 | G | A | 2 | a0001c0001t0001g0083 a0001c0004t0001g0061 |
2 | HG00280.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1510-272C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594065 | |||||||
| chr1:206594096 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
106 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1510-303C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594096 | |||||||
| chr1:206594169 | C | T | 10 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0063 others(7): Show |
13 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1510-376G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594169 | |||||||
| chr1:206594220 | A | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1510-427T>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594220 | |||||||
| chr1:206594318 | G | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1510-525C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594318 | |||||||
| chr1:206594410 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1510-617A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594410 | |||||||
| chr1:206594453 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1510-660T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594453 | |||||||
| chr1:206594589 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1510-796T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594589 | |||||||
| chr1:206594872 | C | T | 2 | a0002c0002t0001g0026 a0002c0002t0001g0166 |
4 | HG01257.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1509+846G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206594872 | |||||||
| chr1:206595024 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(105): Show |
206 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1509+694C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595024 | |||||||
| chr1:206595027 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0018 others(40): Show |
74 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1509+691A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595027 | |||||||
| chr1:206595139 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1509+579G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595139 | |||||||
| chr1:206595339 | G | A | 3 | a0002c0002t0001g0016 a0002c0002t0001g0115 a0002c0002t0001g0116 |
6 | HG02615.hp1 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1509+379C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595339 | |||||||
| chr1:206595361 | A | AGCAAGTT others(4): Show |
13 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(10): Show |
38 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1509+346_1509+356d others(13): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595361 | |||||||
| chr1:206595466 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1509+252T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595466 | |||||||
| chr1:206595497 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1509+221G>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595497 | |||||||
| chr1:206595698 | T | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0018 others(55): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1509+20A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 13/14 | chr1 | 206595698 | |||||||
| chr1:206595979 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1389-141A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206595979 | |||||||
| chr1:206596010 | GTA | G | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389-174_1389-173d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596010 | |||||||
| chr1:206596151 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1389-313T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596151 | |||||||
| chr1:206596212 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1389-374G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596212 | |||||||
| chr1:206596264 | GA | G | 11 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0111 others(8): Show |
13 | HG01109.hp2 HG01123.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1389-427delT | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596264 | |||||||
| chr1:206596348 | G | A | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1389-510C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596348 | |||||||
| chr1:206596388 | A | G | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1389-550T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596388 | |||||||
| chr1:206596423 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1389-585C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596423 | |||||||
| chr1:206596461 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
209 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1389-623G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596461 | |||||||
| chr1:206596535 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
10 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1388+565T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596535 | |||||||
| chr1:206596551 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1388+549A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596551 | |||||||
| chr1:206596803 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1388+297G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596803 | |||||||
| chr1:206596819 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1388+281C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596819 | |||||||
| chr1:206596934 | A | AC | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(105): Show |
206 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1388+165dupG | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206596934 | |||||||
| chr1:206597095 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG04204.hp2 | splice_region_variant&intron_variant | LOW | c.1388+5C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 12/14 | chr1 | 206597095 | |||||||
| chr1:206597252 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1293-57C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597252 | |||||||
| chr1:206597268 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1293-73T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597268 | |||||||
| chr1:206597542 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0114 a0001c0001t0001g0173 |
6 | HG02630.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1293-347A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597542 | |||||||
| chr1:206597597 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(105): Show |
206 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1293-402T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597597 | |||||||
| chr1:206597629 | C | T | 1 | a0001c0001t0001g0021 | 3 | NA18943.hp2 NA18972.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1293-434G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597629 | |||||||
| chr1:206597682 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293-487G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597682 | |||||||
| chr1:206597710 | C | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1293-515G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597710 | |||||||
| chr1:206597737 | G | C | 1 | a0001c0001t0001g0029 | 3 | HG00735.hp2 HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1293-542C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597737 | |||||||
| chr1:206597739 | GT | G | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293-545delA | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597739 | |||||||
| chr1:206597741 | T | G | 1 | a0002c0002t0001g0026 | 3 | HG01257.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1293-546A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597741 | |||||||
| chr1:206597755 | G | C | 1 | a0001c0003t0001g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1293-560C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597755 | |||||||
| chr1:206597802 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1293-607C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597802 | |||||||
| chr1:206597888 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1293-693A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597888 | |||||||
| chr1:206597904 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0048 others(2): Show |
11 | HG02071.hp2 HG02523.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.1293-709G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597904 | |||||||
| chr1:206597906 | T | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0018 others(55): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1293-711A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597906 | |||||||
| chr1:206597991 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0105 |
3 | HG01516.hp1 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1293-796C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206597991 | |||||||
| chr1:206598047 | T | A | 1 | a0002c0002t0001g0133 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1293-852A>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598047 | |||||||
| chr1:206598199 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1292+804C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598199 | |||||||
| chr1:206598249 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0161 |
2 | NA18964.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1292+754C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598249 | |||||||
| chr1:206598268 | C | G | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1292+735G>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598268 | |||||||
| chr1:206598303 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1292+700C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598303 | |||||||
| chr1:206598400 | T | G | 12 | a0001c0001t0001g0027 a0001c0001t0001g0064 a0001c0001t0001g0110 others(9): Show |
14 | HG01109.hp2 HG01123.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1292+603A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598400 | |||||||
| chr1:206598414 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1292+589T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598414 | |||||||
| chr1:206598481 | T | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0063 others(7): Show |
13 | HG00738.hp2 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1292+522A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598481 | |||||||
| chr1:206598516 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1292+487T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598516 | |||||||
| chr1:206598535 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1292+468G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598535 | |||||||
| chr1:206598537 | TAC | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1292+464_1292+465d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598537 | |||||||
| chr1:206598607 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1292+396C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598607 | |||||||
| chr1:206598636 | C | CCA | 49 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(46): Show |
79 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1292+365_1292+366d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598636 | |||||||
| chr1:206598638 | A | ACG | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
209 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1292+364_1292+365i others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598638 | |||||||
| chr1:206598659 | A | G | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1292+344T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598659 | |||||||
| chr1:206598794 | G | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1292+209C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598794 | |||||||
| chr1:206598842 | A | ACT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
209 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1292+159_1292+160d others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598842 | |||||||
| chr1:206598908 | T | C | 1 | a0003c0008t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1292+95A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 11/14 | chr1 | 206598908 | |||||||
| chr1:206599193 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1203-101T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 10/14 | chr1 | 206599193 | |||||||
| chr1:206599286 | G | A | 1 | a0001c0001t0001g0029 | 3 | HG00735.hp2 HG01169.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1202+177C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 10/14 | chr1 | 206599286 | |||||||
| chr1:206599399 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
106 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1202+64C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 10/14 | chr1 | 206599399 | |||||||
| chr1:206599700 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1052+33C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 9/14 | chr1 | 206599700 | |||||||
| chr1:206599701 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1052+32G>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 9/14 | chr1 | 206599701 | |||||||
| chr1:206599941 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.949-105C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 8/14 | chr1 | 206599941 | |||||||
| chr1:206600043 | T | G | 1 | a0001c0001t0001g0038 | 2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.949-207A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 8/14 | chr1 | 206600043 | |||||||
| chr1:206600188 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.948+75C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 8/14 | chr1 | 206600188 | |||||||
| chr1:206600468 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
208 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.903-160A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206600468 | |||||||
| chr1:206600565 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.903-257G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206600565 | |||||||
| chr1:206600633 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.903-325G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206600633 | |||||||
| chr1:206600843 | T | G | 1 | a0001c0001t0001g0157 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.903-535A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206600843 | |||||||
| chr1:206600859 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.903-551T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206600859 | |||||||
| chr1:206600994 | T | C | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.903-686A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206600994 | |||||||
| chr1:206601126 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.903-818G>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601126 | |||||||
| chr1:206601336 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0199 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.902+1000C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601336 | |||||||
| chr1:206601380 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.902+956C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601380 | |||||||
| chr1:206601515 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.902+821C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601515 | |||||||
| chr1:206601519 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.902+817G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601519 | |||||||
| chr1:206601682 | T | A | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.902+654A>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601682 | |||||||
| chr1:206601798 | G | A | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.902+538C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601798 | |||||||
| chr1:206601927 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.902+409G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601927 | |||||||
| chr1:206601966 | A | G | 1 | a0001c0001t0001g0032 | 2 | NA18747.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.902+370T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601966 | |||||||
| chr1:206601976 | T | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.902+360A>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206601976 | |||||||
| chr1:206602036 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(36): Show |
68 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.902+300C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206602036 | |||||||
| chr1:206602073 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(109): Show |
208 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.902+263T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206602073 | |||||||
| chr1:206602082 | G | A | 1 | a0002c0002t0001g0116 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.902+254C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 7/14 | chr1 | 206602082 | |||||||
| chr1:206602461 | G | C | 1 | a0001c0001t0001g0120 | 1 | NA18999.hp2 | splice_region_variant&intron_variant | LOW | c.785-8C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/14 | chr1 | 206602461 | |||||||
| chr1:206602743 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(107): Show |
208 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.784+208T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/14 | chr1 | 206602743 | |||||||
| chr1:206602778 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0137 |
2 | HG00597.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.784+173T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/14 | chr1 | 206602778 | |||||||
| chr1:206602846 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
104 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.784+105A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/14 | chr1 | 206602846 | |||||||
| chr1:206602846 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0095 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.784+105A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/14 | chr1 | 206602846 | |||||||
| chr1:206602855 | A | G | 3 | a0001c0001t0001g0069 a0001c0001t0001g0087 a0001c0001t0001g0095 |
3 | HG02056.hp1 HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.784+96T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 6/14 | chr1 | 206602855 | |||||||
| chr1:206603293 | C | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.531-89G>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603293 | |||||||
| chr1:206603322 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0195 |
3 | HG01074.hp1 HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.531-118T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603322 | |||||||
| chr1:206603441 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.531-237G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603441 | |||||||
| chr1:206603503 | G | T | 2 | a0001c0001t0001g0188 a0001c0001t0002g0051 |
3 | HG01069.hp1 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.531-299C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603503 | |||||||
| chr1:206603587 | G | A | 8 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG01123.hp1 HG02132.hp1 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.531-383C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603587 | |||||||
| chr1:206603613 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(14): Show |
42 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.531-409C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603613 | |||||||
| chr1:206603719 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0094 |
2 | HG01106.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.531-515G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603719 | |||||||
| chr1:206603838 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.531-634A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603838 | |||||||
| chr1:206603843 | A | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.531-639T>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603843 | |||||||
| chr1:206603870 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.531-666G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603870 | |||||||
| chr1:206603871 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(14): Show |
42 | HG00099.hp2 HG00544.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.531-667C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603871 | |||||||
| chr1:206603928 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.531-724C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603928 | |||||||
| chr1:206603942 | CATAA | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00099.hp1 HG00609.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-742_531-739del others(4): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603942 | |||||||
| chr1:206603947 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.531-743T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603947 | |||||||
| chr1:206603970 | G | C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0111 others(8): Show |
13 | HG01109.hp2 HG01123.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.531-766C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603970 | |||||||
| chr1:206603992 | A | G | 1 | a0001c0003t0001g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.531-788T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206603992 | |||||||
| chr1:206604136 | A | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(106): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.531-932T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604136 | |||||||
| chr1:206604180 | C | T | 1 | a0001c0001t0001g0022 | 3 | NA18964.hp2 NA18983.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.531-976G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604180 | |||||||
| chr1:206604225 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.531-1021C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604225 | |||||||
| chr1:206604241 | G | A | 2 | a0001c0001t0001g0059 a0001c0001t0001g0071 |
2 | HG00099.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.531-1037C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604241 | |||||||
| chr1:206604261 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
106 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.531-1057C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604261 | |||||||
| chr1:206604307 | T | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.530+1093A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604307 | |||||||
| chr1:206604336 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.530+1064G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604336 | |||||||
| chr1:206604360 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.530+1040G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604360 | |||||||
| chr1:206604463 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
204 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.530+937T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604463 | |||||||
| chr1:206604591 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.530+809C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604591 | |||||||
| chr1:206604595 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.530+805C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604595 | |||||||
| chr1:206604689 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0162 a0001c0005t0001g0203 |
3 | HG01243.hp1 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.530+711G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604689 | |||||||
| chr1:206604711 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0018 others(37): Show |
69 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.530+689G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604711 | |||||||
| chr1:206604719 | C | T | 9 | a0001c0001t0001g0064 a0001c0001t0001g0111 a0001c0001t0001g0125 others(6): Show |
9 | HG01123.hp1 HG02132.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.530+681G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604719 | |||||||
| chr1:206604732 | C | CA | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(60): Show |
150 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.530+667dupT | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604732 | |||||||
| chr1:206604732 | CA | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(94): Show |
193 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.530+667delT | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604732 | |||||||
| chr1:206604732 | CAA | C | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
7 | HG01993.hp2 HG02280.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.530+666_530+667del others(2): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604732 | |||||||
| chr1:206604790 | G | A | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.530+610C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604790 | |||||||
| chr1:206604810 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.530+590G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604810 | |||||||
| chr1:206604884 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0185 |
5 | HG01109.hp2 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+516T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604884 | |||||||
| chr1:206604899 | G | A | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00099.hp1 HG00609.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+501C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604899 | |||||||
| chr1:206604901 | G | A | 11 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0111 others(8): Show |
13 | HG01109.hp2 HG01123.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+499C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604901 | |||||||
| chr1:206604934 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0208 |
3 | HG02647.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.530+466C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206604934 | |||||||
| chr1:206605006 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.530+394C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206605006 | |||||||
| chr1:206605289 | A | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0018 others(55): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.530+111T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206605289 | |||||||
| chr1:206605361 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.530+39G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 5/14 | chr1 | 206605361 | |||||||
| chr1:206605674 | C | T | 16 | a0001c0001t0001g0027 a0001c0001t0001g0064 a0001c0001t0001g0110 others(13): Show |
18 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.423-167G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206605674 | |||||||
| chr1:206605791 | ATC | A | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.423-286_423-285del others(2): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206605791 | |||||||
| chr1:206605822 | T | C | 1 | a0002c0002t0001g0134 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.423-315A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206605822 | |||||||
| chr1:206605975 | G | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0064 a0001c0001t0001g0110 others(9): Show |
14 | HG01109.hp2 HG01123.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.423-468C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206605975 | |||||||
| chr1:206606000 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.423-493C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606000 | |||||||
| chr1:206606021 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.423-514C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606021 | |||||||
| chr1:206606080 | T | C | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.423-573A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606080 | |||||||
| chr1:206606125 | T | C | 1 | a0001c0003t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.423-618A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606125 | |||||||
| chr1:206606175 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0071 |
3 | HG00099.hp1 HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.423-668C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606175 | |||||||
| chr1:206606204 | G | A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0064 a0001c0001t0001g0110 others(10): Show |
15 | HG01109.hp2 HG01123.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.423-697C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606204 | |||||||
| chr1:206606409 | G | C | 1 | a0001c0003t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.423-902C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606409 | |||||||
| chr1:206606440 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.423-933A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606440 | |||||||
| chr1:206606520 | C | G | 1 | a0002c0002t0001g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.423-1013G>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606520 | |||||||
| chr1:206606531 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0167 a0001c0001t0001g0199 |
4 | HG02055.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-1024A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606531 | |||||||
| chr1:206606563 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
200 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.423-1056C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606563 | |||||||
| chr1:206606745 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.423-1238T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606745 | |||||||
| chr1:206606806 | T | C | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.423-1299A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606806 | |||||||
| chr1:206606860 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.423-1353C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606860 | |||||||
| chr1:206606946 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.422+1290T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206606946 | |||||||
| chr1:206607002 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0124 |
2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.422+1234C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607002 | |||||||
| chr1:206607015 | TAGAGGCA others(3): Show |
T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0208 |
2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.422+1211_422+1220d others(12): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607015 | |||||||
| chr1:206607031 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.422+1205T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607031 | |||||||
| chr1:206607069 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0167 a0001c0001t0001g0199 |
4 | HG02055.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+1167T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607069 | |||||||
| chr1:206607265 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00099.hp1 HG00609.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.422+971T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607265 | |||||||
| chr1:206607289 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.422+947T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607289 | |||||||
| chr1:206607385 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.422+851A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607385 | |||||||
| chr1:206607429 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.422+807G>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607429 | |||||||
| chr1:206607467 | A | C | 1 | a0003c0008t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422+769T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607467 | |||||||
| chr1:206607472 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.422+764A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607472 | |||||||
| chr1:206607518 | C | T | 1 | a0003c0008t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422+718G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607518 | |||||||
| chr1:206607555 | C | T | 1 | a0003c0008t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.422+681G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607555 | |||||||
| chr1:206607566 | C | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG00609.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.422+670G>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607566 | |||||||
| chr1:206607877 | A | C | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+359T>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607877 | |||||||
| chr1:206607974 | A | AAAAAT | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
19 | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.422+257_422+261dup others(5): Show |
EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607974 | |||||||
| chr1:206607984 | T | C | 46 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0011 others(43): Show |
79 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.422+252A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 4/14 | chr1 | 206607984 | |||||||
| chr1:206608379 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.332-53G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608379 | |||||||
| chr1:206608404 | C | T | 1 | a0002c0002t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.332-78G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608404 | |||||||
| chr1:206608428 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.332-102C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608428 | |||||||
| chr1:206608533 | C | T | 3 | a0001c0003t0001g0070 a0001c0003t0001g0186 a0001c0003t0001g0187 |
3 | HG02109.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.332-207G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608533 | |||||||
| chr1:206608600 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.332-274C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608600 | |||||||
| chr1:206608665 | C | T | 1 | a0003c0008t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.332-339G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608665 | |||||||
| chr1:206608688 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.332-362C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608688 | |||||||
| chr1:206608829 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0109 |
6 | HG01884.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-503A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608829 | |||||||
| chr1:206608831 | G | C | 25 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0057 others(22): Show |
27 | HG00099.hp1 HG00609.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-505C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608831 | |||||||
| chr1:206608895 | T | C | 1 | a0001c0007t0001g0163 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.331+481A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608895 | |||||||
| chr1:206608919 | A | G | 21 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0057 others(18): Show |
23 | HG00099.hp1 HG00609.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.331+457T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206608919 | |||||||
| chr1:206609051 | CA | C | 21 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0057 others(18): Show |
23 | HG00099.hp1 HG00609.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.331+324delT | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206609051 | |||||||
| chr1:206609059 | A | T | 12 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0111 others(9): Show |
15 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.331+317T>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206609059 | |||||||
| chr1:206609060 | A | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(47): Show |
109 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.331+316T>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 3/14 | chr1 | 206609060 | |||||||
| chr1:206609669 | G | A | 7 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
7 | HG01123.hp1 HG02132.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-210C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206609669 | |||||||
| chr1:206609791 | T | C | 1 | a0002c0002t0001g0034 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.248-332A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206609791 | |||||||
| chr1:206609954 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.248-495A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206609954 | |||||||
| chr1:206609955 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.248-496C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206609955 | |||||||
| chr1:206610052 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.248-593T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610052 | |||||||
| chr1:206610114 | T | G | 13 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0130 others(10): Show |
17 | HG01257.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.248-655A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610114 | |||||||
| chr1:206610360 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.247+824T>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610360 | |||||||
| chr1:206610424 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
110 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.247+760A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610424 | |||||||
| chr1:206610434 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.247+750G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610434 | |||||||
| chr1:206610546 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.247+638G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610546 | |||||||
| chr1:206610592 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0208 |
3 | HG03139.hp1 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.247+592C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610592 | |||||||
| chr1:206610602 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(13): Show |
31 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+582A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610602 | |||||||
| chr1:206610620 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(13): Show |
31 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+564T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610620 | |||||||
| chr1:206610676 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(13): Show |
31 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+508G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610676 | |||||||
| chr1:206610690 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0168 |
3 | HG01516.hp1 HG01517.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.247+494C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610690 | |||||||
| chr1:206610706 | T | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(13): Show |
31 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+478A>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610706 | |||||||
| chr1:206610713 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.247+471G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610713 | |||||||
| chr1:206610752 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.247+432G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610752 | |||||||
| chr1:206610778 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0047 others(13): Show |
28 | HG00544.hp2 HG00673.hp2 HG02630.hp1 others(25): Show |
intron_variant | MODIFIER | c.247+406C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610778 | |||||||
| chr1:206610815 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(13): Show |
31 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+369A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610815 | |||||||
| chr1:206610824 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(13): Show |
31 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+360T>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610824 | |||||||
| chr1:206610879 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0063 |
3 | HG02622.hp1 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.247+305G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610879 | |||||||
| chr1:206610930 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.247+254G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206610930 | |||||||
| chr1:206611108 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.247+76A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 2/14 | chr1 | 206611108 | |||||||
| chr1:206611438 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | NA18984.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.57-64C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206611438 | |||||||
| chr1:206611438 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.57-64C>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206611438 | |||||||
| chr1:206611438 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.57-64C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206611438 | |||||||
| chr1:206611456 | T | C | 16 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0050 others(13): Show |
24 | HG00140.hp1 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.57-82A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206611456 | |||||||
| chr1:206611485 | G | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(2): Show |
5 | HG00099.hp1 HG00609.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-111C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206611485 | |||||||
| chr1:206611595 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.57-221A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206611595 | |||||||
| chr1:206611667 | T | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(14): Show |
32 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.57-293A>G | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206611667 | |||||||
| chr1:206612039 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.56+248C>T | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206612039 | |||||||
| chr1:206612049 | T | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0054 others(14): Show |
32 | HG00735.hp2 HG01070.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.56+238A>C | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206612049 | |||||||
| chr1:206612225 | C | T | 1 | a0002c0002t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.56+62G>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206612225 | |||||||
| chr1:206612244 | G | T | 1 | a0002c0002t0001g0055 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.56+43C>A | EIF2D | ENSG00000143486.16 | transcript | ENST00000271764.7 | protein_coding | 1/14 | chr1 | 206612244 |