Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79833 |
| ensemblid | ENSG00000152147.11 |
| hgncid | 20044 |
| symbol | GEMIN6 |
| name | gem nuclear organelle associated protein 6 |
| refseq_nuc | NM_024775.10 |
| refseq_prot | NP_079051.9 |
| ensembl_nuc | ENST00000281950.8 |
| ensembl_prot | ENSP00000281950.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 38778210 |
| end | 38785002 |
| strand | + |
| ver | v1.2 |
| region | chr2:38778210-38785002 |
| region5000 | chr2:38773210-38790002 |
| regionname0 | GEMIN6_chr2_38778210_38785002 |
| regionname5000 | GEMIN6_chr2_38773210_38790002 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 167 | 328 | 94 | 61 | 122 | 14 | 35 | 89 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | MSEWM others(162): Show |
chr2 | 38773210 | 38790002 |
| a0002 | 0/0 | 167 | 83 | 0 | 9 | 63 | 2 | 9 | 56 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | MSEWM others(162): Show |
chr2 | 38773210 | 38790002 |
| a0003 | 0/0 | 167 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | MSEWM others(162): Show |
chr2 | 38773210 | 38790002 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 501 | 324 | 93 | 61 | 121 | 13 | 34 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | ATGAG others(496): Show |
chr2 | 38773210 | 38790002 | ||
| a0001c0003 | 0/0 | 501 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | ATGAG others(496): Show |
chr2 | 38773210 | 38790002 | ||
| a0001c0004 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | ATGAG others(496): Show |
chr2 | 38773210 | 38790002 | ||
| a0001c0005 | 0/0 | 501 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | ATGAG others(496): Show |
chr2 | 38773210 | 38790002 | ||
| a0001c0006 | 0/0 | 501 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | ATGAG others(496): Show |
chr2 | 38773210 | 38790002 | ||
| a0002c0002 | 0/0 | 501 | 83 | 0 | 9 | 63 | 2 | 9 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | ATGAG others(496): Show |
chr2 | 38773210 | 38790002 | ||
| a0003c0007 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | ATGAG others(496): Show |
chr2 | 38773210 | 38790002 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3704 | 135 | 20 | 27 | 69 | 6 | 13 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0002 | 0/0 | 3700 | 43 | 19 | 6 | 4 | 2 | 12 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0003 | 0/0 | 3704 | 19 | 16 | 3 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0004 | 0/0 | 3700 | 15 | 0 | 7 | 6 | 0 | 2 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0005 | 0/0 | 3699 | 11 | 0 | 6 | 0 | 3 | 2 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3694): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0007 | 1/0 | 3705 | 9 | 8 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0008 | 0/0 | 3700 | 8 | 0 | 0 | 8 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0009 | 0/0 | 3700 | 7 | 0 | 0 | 7 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0010 | 0/0 | 3701 | 6 | 0 | 0 | 6 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3696): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0011 | 0/0 | 3701 | 6 | 6 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3696): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0012 | 0/0 | 3700 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0013 | 0/0 | 3705 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0014 | 0/0 | 3705 | 3 | 0 | 0 | 1 | 0 | 2 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0015 | 0/0 | 3703 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3698): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0016 | 0/0 | 3696 | 4 | 4 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3691): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0017 | 0/0 | 3704 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0018 | 0/0 | 3701 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3696): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0019 | 0/0 | 3702 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3697): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0020 | 0/0 | 3699 | 2 | 0 | 0 | 1 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3694): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0021 | 0/0 | 3699 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3694): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0022 | 0/0 | 3705 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0023 | 0/0 | 3703 | 2 | 0 | 0 | 1 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3698): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0024 | 0/0 | 3700 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0025 | 0/0 | 3704 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0026 | 0/0 | 3704 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCA others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0027 | 0/0 | 3704 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0028 | 0/0 | 3704 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0029 | 0/1 | 3700 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0030 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0031 | 0/0 | 3702 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3697): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0032 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0033 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3701): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0034 | 0/0 | 3701 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3696): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0035 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3701): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0036 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0037 | 0/0 | 3701 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3696): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0038 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0039 | 0/0 | 3702 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3697): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0040 | 0/0 | 3701 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3696): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0042 | 0/0 | 3690 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3685): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0043 | 0/0 | 3699 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3694): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0044 | 0/0 | 3699 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3694): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0045 | 0/0 | 3704 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0047 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0048 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0049 | 0/0 | 3704 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0052 | 0/0 | 3703 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3698): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0053 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0057 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0058 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3695): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0059 | 0/0 | 3703 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3698): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0060 | 0/0 | 3701 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3696): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0061 | 0/0 | 3698 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3693): Show |
chr2 | 38773210 | 38790002 |
| a0001c0001t0062 | 0/0 | 3704 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0003t0001 | 0/0 | 3704 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0004t0001 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0005t0001 | 0/0 | 3704 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0001c0006t0041 | 0/0 | 3703 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3698): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0001 | 0/0 | 3704 | 59 | 0 | 7 | 42 | 2 | 8 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0006 | 0/0 | 3704 | 11 | 0 | 0 | 11 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0013 | 0/0 | 3705 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0014 | 0/0 | 3705 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0022 | 0/0 | 3705 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0046 | 0/0 | 3706 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3701): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0050 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0051 | 0/0 | 3704 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0054 | 0/0 | 3705 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3700): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0055 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| a0002c0002t0056 | 0/0 | 3703 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3698): Show |
chr2 | 38773210 | 38790002 |
| a0003c0007t0001 | 0/0 | 3704 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | GGTCT others(3699): Show |
chr2 | 38773210 | 38790002 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 107 | 17 | 24 | 48 | 6 | 12 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0002 | 0/0 | 15 | 1 | 2 | 12 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0008 | 0/0 | 6 | 5 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0012 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0013 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0003g0003 | 0/0 | 13 | 11 | 2 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0004 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0005g0010 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0007g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0007g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0007g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0008g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0009g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0009g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0010g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0010g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0011g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0012g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0012g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0012g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0013g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0014g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0015g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0015g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0016g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0016g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0017g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0017g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0017g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0018g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0018g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0019g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0020g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0020g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0021g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0021g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0022g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0023g0001 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0024g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0025g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0026g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0027g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0028g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0029g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0030g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0031g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0032g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0033g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0034g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0035g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0036g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0037g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0038g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0039g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0040g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0042g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0043g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0044g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0045g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0047g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0048g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0049g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0052g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0053g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0057g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0058g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0059g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0060g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0061g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0001t0062g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0003t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0004t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0001c0006t0041g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0001g0001 | 0/0 | 43 | 0 | 7 | 28 | 2 | 6 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0006g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0006g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0013g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0014g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0022g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0046g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0050g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0051g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0054g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0055g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0002c0002t0056g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| a0003c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | FIN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00323 | hp2 | a0001 | c0005 | t0001 | g0001 | EUR | FIN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00597 | hp1 | a0002 | c0002 | t0006 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00609 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00642 | hp1 | a0001 | c0001 | t0025 | g0031 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00673 | hp1 | a0001 | c0001 | t0012 | g0014 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01069 | hp1 | a0002 | c0002 | t0022 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01069 | hp2 | a0001 | c0001 | t0052 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01070 | hp2 | a0001 | c0001 | t0024 | g0027 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01071 | hp1 | a0001 | c0001 | t0024 | g0027 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01106 | hp1 | a0001 | c0001 | t0030 | g0011 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0041 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01167 | hp1 | a0001 | c0001 | t0043 | g0010 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01168 | hp1 | a0001 | c0001 | t0025 | g0031 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01192 | hp2 | a0001 | c0001 | t0019 | g0004 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01257 | hp1 | a0001 | c0001 | t0021 | g0004 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0015 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01358 | hp2 | a0001 | c0001 | t0038 | g0004 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01433 | hp2 | a0001 | c0001 | t0026 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0010 | EUR | IBS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0001 | EUR | IBS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0001 | EUR | IBS | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01981 | hp1 | a0002 | c0002 | t0046 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02015 | hp1 | a0001 | c0001 | t0047 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02040 | hp2 | a0002 | c0002 | t0055 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02080 | hp1 | a0001 | c0001 | t0053 | g0002 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02145 | hp1 | a0001 | c0001 | t0011 | g0068 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0085 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | CDX | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02165 | hp2 | a0002 | c0002 | t0006 | g0009 | EAS | CDX | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02258 | hp1 | a0001 | c0001 | t0016 | g0039 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02451 | hp1 | a0001 | c0001 | t0016 | g0011 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02523 | hp1 | a0001 | c0001 | t0012 | g0004 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0034 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02630 | hp2 | a0001 | c0001 | t0016 | g0025 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02723 | hp2 | a0001 | c0001 | t0059 | g0061 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0069 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02735 | hp2 | a0001 | c0001 | t0014 | g0002 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02738 | hp2 | a0001 | c0001 | t0014 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02809 | hp1 | a0001 | c0001 | t0042 | g0075 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02886 | hp2 | a0001 | c0001 | t0033 | g0036 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0076 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0011 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0020 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03041 | hp2 | a0001 | c0001 | t0045 | g0003 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03130 | hp1 | a0001 | c0001 | t0015 | g0032 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03225 | hp2 | a0001 | c0001 | t0035 | g0080 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03453 | hp1 | a0001 | c0001 | t0018 | g0043 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03486 | hp2 | a0001 | c0001 | t0013 | g0001 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0032 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | ESN | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03579 | hp1 | a0001 | c0001 | t0017 | g0083 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03654 | hp1 | a0001 | c0001 | t0018 | g0015 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03834 | hp1 | a0002 | c0002 | t0051 | g0001 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | BEB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04199 | hp1 | a0001 | c0001 | t0037 | g0021 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | YRI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | YRI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18612 | hp2 | a0001 | c0001 | t0012 | g0026 | EAS | CHB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18747 | hp2 | a0001 | c0001 | t0021 | g0012 | EAS | CHB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18906 | hp2 | a0001 | c0001 | t0015 | g0079 | AFR | YRI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18943 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18951 | hp2 | a0001 | c0001 | t0040 | g0004 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18956 | hp2 | a0001 | c0001 | t0010 | g0065 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18961 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18961 | hp2 | a0001 | c0001 | t0057 | g0022 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18963 | hp2 | a0001 | c0001 | t0060 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18964 | hp2 | a0002 | c0002 | t0013 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18966 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18967 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18969 | hp1 | a0002 | c0002 | t0013 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18971 | hp2 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18972 | hp2 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18974 | hp2 | a0001 | c0001 | t0058 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18977 | hp1 | a0002 | c0002 | t0014 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18977 | hp2 | a0002 | c0002 | t0014 | g0019 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18982 | hp1 | a0001 | c0001 | t0036 | g0017 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18983 | hp2 | a0001 | c0001 | t0020 | g0021 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18985 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18988 | hp1 | a0001 | c0001 | t0009 | g0021 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18988 | hp2 | a0001 | c0001 | t0014 | g0023 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18989 | hp1 | a0002 | c0002 | t0013 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18989 | hp2 | a0001 | c0001 | t0023 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18991 | hp2 | a0001 | c0001 | t0019 | g0070 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18994 | hp1 | a0002 | c0002 | t0013 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18995 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18997 | hp1 | a0001 | c0001 | t0034 | g0064 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19002 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19003 | hp2 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19009 | hp1 | a0002 | c0002 | t0006 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19010 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19010 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19030 | hp2 | a0001 | c0001 | t0049 | g0001 | AFR | LWK | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | LWK | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | LWK | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19057 | hp1 | a0001 | c0001 | t0012 | g0044 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19057 | hp2 | a0002 | c0002 | t0056 | g0073 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19058 | hp1 | a0002 | c0002 | t0006 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19062 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19063 | hp2 | a0003 | c0007 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19065 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19066 | hp2 | a0002 | c0002 | t0006 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19067 | hp2 | a0002 | c0002 | t0054 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19068 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19075 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19079 | hp1 | a0001 | c0001 | t0048 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19083 | hp2 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19084 | hp1 | a0001 | c0001 | t0032 | g0004 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19087 | hp2 | a0002 | c0002 | t0050 | g0023 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19088 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19089 | hp1 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19090 | hp1 | a0002 | c0002 | t0006 | g0009 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19091 | hp1 | a0001 | c0001 | t0061 | g0006 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | YRI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0016 | AFR | YRI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20129 | hp1 | a0001 | c0001 | t0062 | g0034 | AFR | ASW | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20752 | hp1 | a0001 | c0001 | t0020 | g0008 | EUR | TSI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0013 | EUR | TSI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0010 | EUR | TSI | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20905 | hp1 | a0001 | c0001 | t0044 | g0010 | SAS | GIH | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01123 | hp1 | a0001 | c0001 | t0028 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0072 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02486 | hp1 | a0001 | c0001 | t0039 | g0008 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02559 | hp1 | a0001 | c0006 | t0041 | g0084 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG02559 | hp2 | a0001 | c0001 | t0015 | g0082 | AFR | ACB | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG03471 | hp2 | a0001 | c0001 | t0031 | g0066 | AFR | MSL | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0016 | AFR | USA | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| HG06807 | hp2 | a0001 | c0001 | t0022 | g0001 | AFR | USA | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | USA | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | LWK | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0050 | REF | REF | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0003 | REF | REF | GEMIN6_chr2_38773210_38790002 | GEMIN6 | chr2 | 38773210 | 38790002 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38781599 | A | G | 1 | a0003 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.211A>G | p.Met71Val | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 302/3705 | 211/504 | 71/167 | chr2 | 38781599 | |||
| chr2:38781807 | G | A | 1 | a0002 | 83 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
missense_variant | MODERATE | c.419G>A | p.Gly140Asp | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 510/3705 | 419/504 | 140/167 | chr2 | 38781807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38781604 | T | C | 1 | a0001c0003 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.216T>C | p.Asn72Asn | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 307/3705 | 216/504 | 72/167 | chr2 | 38781604 | |||
| chr2:38781649 | G | A | 1 | a0001c0004 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.261G>A | p.Thr87Thr | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 352/3705 | 261/504 | 87/167 | chr2 | 38781649 | |||
| chr2:38781847 | G | T | 1 | a0001c0006 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.459G>T | p.Ser153Ser | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 550/3705 | 459/504 | 153/167 | chr2 | 38781847 | |||
| chr2:38781883 | T | A | 1 | a0001c0005 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.495T>A | p.Ala165Ala | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 586/3705 | 495/504 | 165/167 | chr2 | 38781883 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38778214 | T | A | 1 | a0001c0001t0026 | 1 | HG01433.hp2 | 5_prime_UTR_variant | MODIFIER | c.-87T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 1/3 | 777 | chr2 | 38778214 | ||||||
| chr2:38778221 | A | G | 1 | a0001c0001t0062 | 1 | NA20129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80A>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 1/3 | 770 | chr2 | 38778221 | ||||||
| chr2:38778274 | T | A | 1 | a0001c0001t0027 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-27T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 1/3 | 717 | chr2 | 38778274 | ||||||
| chr2:38778975 | T | C | 1 | a0001c0001t0028 | 1 | HG01123.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/3 | 16 | chr2 | 38778975 | ||||||
| chr2:38781981 | G | T | 3 | a0001c0001t0008 a0001c0001t0060 a0001c0001t0061 |
10 | NA18943.hp2 NA18946.hp1 NA18961.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*89G>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 89 | chr2 | 38781981 | ||||||
| chr2:38782038 | G | A | 1 | a0001c0001t0012 | 5 | HG00609.hp1 HG00673.hp1 HG02523.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*146G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 146 | chr2 | 38782038 | ||||||
| chr2:38782081 | A | C | 1 | a0001c0001t0059 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189A>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 189 | chr2 | 38782081 | ||||||
| chr2:38782137 | C | T | 1 | a0001c0001t0058 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 245 | chr2 | 38782137 | ||||||
| chr2:38782138 | T | C | 1 | a0001c0001t0058 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 246 | chr2 | 38782138 | ||||||
| chr2:38782216 | T | C | 2 | a0001c0001t0030 a0001c0001t0031 |
2 | HG01106.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*324T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 324 | chr2 | 38782216 | ||||||
| chr2:38782251 | C | T | 1 | a0001c0001t0057 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*359C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 359 | chr2 | 38782251 | ||||||
| chr2:38782269 | G | A | 1 | a0001c0001t0032 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 377 | chr2 | 38782269 | ||||||
| chr2:38782364 | A | T | 1 | a0001c0001t0059 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472A>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 472 | chr2 | 38782364 | ||||||
| chr2:38782392 | C | T | 1 | a0001c0001t0025 | 2 | HG00642.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*500C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 500 | chr2 | 38782392 | ||||||
| chr2:38782611 | C | T | 4 | a0002c0002t0006 a0002c0002t0054 a0002c0002t0055 others(1): Show |
14 | HG00597.hp1 HG02040.hp2 HG02165.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*719C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 719 | chr2 | 38782611 | ||||||
| chr2:38782713 | C | T | 1 | a0001c0001t0053 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*821C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 821 | chr2 | 38782713 | ||||||
| chr2:38782721 | C | T | 1 | a0001c0001t0024 | 2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 829 | chr2 | 38782721 | ||||||
| chr2:38782745 | C | T | 29 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(26): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*853C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 853 | chr2 | 38782745 | ||||||
| chr2:38782765 | C | G | 1 | a0001c0001t0045 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*873C>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 873 | chr2 | 38782765 | ||||||
| chr2:38782766 | T | C | 2 | a0001c0001t0017 a0001c0001t0062 |
4 | HG02630.hp1 HG02922.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*874T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 874 | chr2 | 38782766 | ||||||
| chr2:38782796 | C | CA | 12 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0018 others(9): Show |
19 | HG01192.hp2 HG01981.hp1 HG02630.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*921dupA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 922 | INFO_REALIGN_3_PRIME | chr2 | 38782796 | |||||
| chr2:38782796 | CA | C | 8 | a0001c0001t0005 a0001c0001t0023 a0001c0001t0031 others(5): Show |
19 | HG01069.hp2 HG01099.hp1 HG01109.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*921delA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 921 | INFO_REALIGN_3_PRIME | chr2 | 38782796 | |||||
| chr2:38783036 | T | G | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1144T>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1144 | chr2 | 38783036 | ||||||
| chr2:38783076 | G | A | 4 | a0001c0001t0010 a0001c0001t0034 a0001c0001t0036 others(1): Show |
9 | NA18952.hp1 NA18956.hp2 NA18961.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1184G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1184 | chr2 | 38783076 | ||||||
| chr2:38783091 | A | G | 1 | a0002c0002t0051 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1199A>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1199 | chr2 | 38783091 | ||||||
| chr2:38783128 | C | A | 1 | a0001c0001t0058 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1236C>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1236 | chr2 | 38783128 | ||||||
| chr2:38783152 | G | A | 1 | a0001c0001t0059 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1260 | chr2 | 38783152 | ||||||
| chr2:38783162 | G | T | 28 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0014 others(25): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*1270G>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1270 | chr2 | 38783162 | ||||||
| chr2:38783163 | C | T | 1 | a0002c0002t0050 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1271 | chr2 | 38783163 | ||||||
| chr2:38783165 | C | T | 3 | a0001c0001t0033 a0001c0001t0044 a0001c0001t0049 |
3 | HG02886.hp2 NA19030.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1273C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1273 | chr2 | 38783165 | ||||||
| chr2:38783167 | G | T | 2 | a0001c0001t0031 a0001c0001t0059 |
2 | HG02723.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275G>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1275 | chr2 | 38783167 | ||||||
| chr2:38783176 | T | G | 2 | a0001c0001t0031 a0001c0001t0059 |
2 | HG02723.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1284T>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1284 | chr2 | 38783176 | ||||||
| chr2:38783184 | TTTTG | T | 1 | a0001c0001t0016 | 4 | HG02258.hp1 HG02451.hp1 HG02630.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1308_*1311delGTTT | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1308 | INFO_REALIGN_3_PRIME | chr2 | 38783184 | |||||
| chr2:38783386 | A | C | 1 | a0001c0001t0027 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494A>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1494 | chr2 | 38783386 | ||||||
| chr2:38783479 | G | A | 5 | a0001c0001t0010 a0001c0001t0033 a0001c0001t0034 others(2): Show |
10 | HG02886.hp2 NA18952.hp1 NA18956.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1587G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1587 | chr2 | 38783479 | ||||||
| chr2:38783487 | CTT | C | 6 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0031 others(3): Show |
11 | HG02559.hp1 HG02559.hp2 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1617_*1618delTT | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1617 | INFO_REALIGN_3_PRIME | chr2 | 38783487 | |||||
| chr2:38783487 | CTTTT | C | 5 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0019 others(2): Show |
16 | HG01192.hp2 HG02145.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1615_*1618delTTTT | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1615 | INFO_REALIGN_3_PRIME | chr2 | 38783487 | |||||
| chr2:38783487 | CTTTTT | C | 17 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(14): Show |
105 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1614_*1618delTTTT others(1): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1614 | INFO_REALIGN_3_PRIME | chr2 | 38783487 | |||||
| chr2:38783487 | CTTTTTT | C | 4 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0058 others(1): Show |
6 | HG01257.hp1 NA18747.hp2 NA18974.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1613_*1618delTTTT others(2): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1613 | INFO_REALIGN_3_PRIME | chr2 | 38783487 | |||||
| chr2:38783506 | TTTTTA | T | 29 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(26): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*1615_*1619delTTTT others(1): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1615 | chr2 | 38783506 | ||||||
| chr2:38783507 | TTTTA | T | 5 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0036 others(2): Show |
12 | HG01074.hp2 HG01099.hp2 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1616_*1619delTTTA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1616 | chr2 | 38783507 | ||||||
| chr2:38783611 | G | A | 1 | a0001c0001t0052 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1719G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1719 | chr2 | 38783611 | ||||||
| chr2:38783703 | A | G | 1 | a0001c0001t0043 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1811A>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 1811 | chr2 | 38783703 | ||||||
| chr2:38783923 | C | G | 5 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0032 others(2): Show |
20 | HG00639.hp1 HG00741.hp1 HG01081.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2031C>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2031 | chr2 | 38783923 | ||||||
| chr2:38784016 | G | A | 1 | a0001c0001t0033 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2124G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2124 | chr2 | 38784016 | ||||||
| chr2:38784288 | C | G | 1 | a0001c0001t0038 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2396C>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2396 | chr2 | 38784288 | ||||||
| chr2:38784293 | C | G | 2 | a0001c0001t0009 a0001c0001t0058 |
8 | NA18960.hp2 NA18974.hp2 NA18988.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2401C>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2401 | chr2 | 38784293 | ||||||
| chr2:38784377 | T | TA | 5 | a0001c0001t0014 a0001c0001t0037 a0001c0001t0039 others(2): Show |
8 | HG02486.hp1 HG02735.hp2 HG02738.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2499dupA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2500 | INFO_REALIGN_3_PRIME | chr2 | 38784377 | |||||
| chr2:38784415 | C | T | 1 | a0001c0006t0041 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2523C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2523 | chr2 | 38784415 | ||||||
| chr2:38784470 | G | C | 1 | a0002c0002t0055 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2578G>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2578 | chr2 | 38784470 | ||||||
| chr2:38784507 | G | C | 1 | a0001c0001t0047 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2615G>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2615 | chr2 | 38784507 | ||||||
| chr2:38784530 | CA | C | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(26): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*2653delA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2653 | INFO_REALIGN_3_PRIME | chr2 | 38784530 | |||||
| chr2:38784606 | C | T | 4 | a0001c0001t0010 a0001c0001t0034 a0001c0001t0036 others(1): Show |
9 | NA18952.hp1 NA18956.hp2 NA18961.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2714C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2714 | chr2 | 38784606 | ||||||
| chr2:38784693 | GTGTAAAC others(7): Show |
G | 1 | a0001c0001t0042 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2802_*2815delTGTA others(10): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2802 | chr2 | 38784693 | ||||||
| chr2:38784838 | C | T | 2 | a0001c0001t0009 a0001c0001t0058 |
8 | NA18960.hp2 NA18974.hp2 NA18988.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2946C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 2946 | chr2 | 38784838 | ||||||
| chr2:38784995 | G | A | 1 | a0001c0001t0048 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3103G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 3/3 | 3103 | chr2 | 38784995 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:38778567 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-20+286C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 1/2 | chr2 | 38778567 | |||||||
| chr2:38778643 | G | A | 1 | a0001c0001t0033g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-19-329G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 1/2 | chr2 | 38778643 | |||||||
| chr2:38778769 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-19-203A>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 1/2 | chr2 | 38778769 | |||||||
| chr2:38778786 | T | C | 2 | a0002c0002t0001g0019 a0002c0002t0014g0019 |
3 | NA18977.hp2 NA19065.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-19-186T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 1/2 | chr2 | 38778786 | |||||||
| chr2:38779355 | C | T | 1 | a0001c0001t0011g0016 | 5 | HG02818.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+237C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779355 | |||||||
| chr2:38779461 | T | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.128+343T>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779461 | |||||||
| chr2:38779505 | A | C | 1 | a0002c0002t0056g0073 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.128+387A>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779505 | |||||||
| chr2:38779526 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.128+408G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779526 | |||||||
| chr2:38779596 | C | A | 2 | a0001c0001t0003g0074 a0001c0001t0042g0075 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.128+478C>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779596 | |||||||
| chr2:38779615 | T | A | 2 | a0002c0002t0006g0009 a0002c0002t0056g0073 |
8 | HG02165.hp2 NA18966.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+497T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779615 | |||||||
| chr2:38779636 | C | A | 1 | a0001c0001t0017g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128+518C>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779636 | |||||||
| chr2:38779636 | C | CTA | 3 | a0001c0001t0003g0033 a0001c0001t0010g0022 a0001c0001t0057g0022 |
5 | HG03579.hp2 NA18961.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+546_128+547dup others(2): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | C | CTATA | 3 | a0001c0001t0002g0048 a0001c0001t0002g0054 a0001c0001t0015g0032 |
4 | HG00280.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+544_128+547dup others(4): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | C | CTATATA | 18 | a0001c0001t0002g0004 a0001c0001t0002g0013 a0001c0001t0002g0055 others(15): Show |
28 | HG00609.hp1 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.128+542_128+547dup others(6): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | C | CTATATAT others(1): Show |
10 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0004g0014 others(7): Show |
18 | HG00673.hp1 HG01175.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.128+540_128+547dup others(8): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | C | CTATATAT others(3): Show |
11 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0028 others(8): Show |
17 | HG01106.hp1 HG01516.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.128+538_128+547dup others(10): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | C | CTATATAT others(5): Show |
2 | a0001c0001t0002g0052 a0001c0001t0003g0078 |
2 | HG00741.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.128+536_128+547dup others(12): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | C | CTATATAT others(7): Show |
2 | a0001c0001t0002g0042 a0001c0001t0016g0039 |
2 | HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.128+534_128+547dup others(14): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | CTA | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0014g0002 others(6): Show |
24 | HG01081.hp2 HG01433.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.128+546_128+547del others(2): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779636 | CTATATAT others(9): Show |
C | 1 | a0001c0001t0007g0035 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.128+532_128+547del others(16): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779636 | ||||||
| chr2:38779647 | TATATATA others(8): Show |
T | 1 | a0001c0001t0007g0024 | 3 | HG02723.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.128+530_128+544del others(15): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779647 | |||||||
| chr2:38779647 | TATATATA others(10): Show |
T | 1 | a0001c0001t0007g0085 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.128+530_128+546del others(17): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779647 | |||||||
| chr2:38779652 | ATATATAT others(6): Show |
A | 1 | a0001c0006t0041g0084 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.128+536_128+548del others(13): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779652 | ||||||
| chr2:38779654 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0033g0036 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.128+538_128+553del others(16): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779654 | ||||||
| chr2:38779656 | ATATATAT others(9): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.128+540_128+555del others(16): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779656 | ||||||
| chr2:38779657 | TA | T | 2 | a0001c0001t0001g0001 a0001c0001t0023g0001 |
7 | HG00673.hp2 HG01255.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+540delA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779657 | |||||||
| chr2:38779658 | A | AT | 3 | a0001c0001t0001g0001 a0001c0001t0014g0001 a0001c0001t0049g0001 |
5 | HG01981.hp2 HG02738.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+541dupT | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779658 | ||||||
| chr2:38779658 | A | T | 3 | a0001c0001t0001g0001 a0002c0002t0001g0001 a0002c0002t0001g0005 |
5 | HG00423.hp1 HG00609.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+540A>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779658 | |||||||
| chr2:38779659 | TA | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0086 others(3): Show |
33 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.128+542delA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779659 | |||||||
| chr2:38779659 | TATA | T | 1 | a0001c0001t0001g0001 | 4 | HG01243.hp1 HG01884.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+542_128+544del others(3): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779659 | |||||||
| chr2:38779660 | A | AT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0022g0001 others(6): Show |
15 | HG00099.hp1 HG00642.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.128+543dupT | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779660 | ||||||
| chr2:38779660 | A | ATT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0002c0002t0001g0001 |
6 | HG01517.hp1 HG02074.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+543_128+544ins others(2): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779660 | ||||||
| chr2:38779660 | A | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0063 others(10): Show |
42 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.128+542A>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779660 | |||||||
| chr2:38779660 | ATATATTT others(7): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.128+544_128+557del others(14): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779660 | ||||||
| chr2:38779661 | TA | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0067 others(7): Show |
27 | HG00323.hp2 HG00597.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.128+544delA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779661 | |||||||
| chr2:38779661 | TATA | T | 2 | a0001c0001t0001g0001 a0001c0001t0058g0001 |
3 | HG03139.hp2 NA18974.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.128+544_128+546del others(3): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779661 | |||||||
| chr2:38779662 | A | AT | 5 | a0001c0001t0001g0001 a0001c0001t0003g0003 a0001c0001t0028g0001 others(2): Show |
8 | HG01123.hp1 HG01261.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+545dupT | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779662 | ||||||
| chr2:38779662 | A | ATT | 6 | a0001c0001t0001g0001 a0001c0001t0011g0068 a0002c0002t0001g0001 others(3): Show |
8 | HG02145.hp1 HG02698.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+545_128+546ins others(2): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779662 | ||||||
| chr2:38779662 | A | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(33): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.128+544A>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779662 | |||||||
| chr2:38779662 | ATATTTTT others(7): Show |
A | 1 | a0001c0001t0031g0066 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.128+546_128+559del others(14): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779662 | ||||||
| chr2:38779664 | A | ATATATAT others(44): Show |
1 | a0001c0001t0008g0006 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(51): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(34): Show |
1 | a0001c0001t0008g0006 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(41): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(24): Show |
1 | a0001c0001t0017g0076 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(31): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(22): Show |
1 | a0001c0001t0061g0006 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(29): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(23): Show |
1 | a0001c0001t0008g0006 | 2 | NA19010.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.128+547_128+548ins others(30): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(24): Show |
1 | a0001c0001t0008g0006 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(31): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(27): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(24): Show |
1 | a0001c0001t0008g0006 | 2 | NA18943.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.128+547_128+548ins others(31): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(13): Show |
1 | a0001c0001t0017g0083 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(20): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(22): Show |
1 | a0001c0001t0060g0006 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(29): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(25): Show |
1 | a0001c0001t0008g0006 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(32): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(10): Show |
1 | a0001c0001t0005g0010 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(17): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0003 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(12): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(6): Show |
1 | a0001c0001t0043g0010 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(13): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(7): Show |
1 | a0001c0001t0044g0010 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(14): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(8): Show |
1 | a0001c0001t0005g0010 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(15): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(9): Show |
1 | a0001c0001t0005g0010 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(16): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(8): Show |
1 | a0001c0001t0005g0010 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(15): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(9): Show |
1 | a0001c0001t0020g0008 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(16): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0008 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(12): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | ATATATTT others(6): Show |
1 | a0001c0001t0039g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.128+547_128+548ins others(13): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779664 | A | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(53): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.128+546A>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779664 | |||||||
| chr2:38779664 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0059g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.128+560_128+573del others(14): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38779664 | ||||||
| chr2:38779665 | T | TA | 3 | a0001c0001t0003g0074 a0001c0001t0010g0017 a0001c0001t0036g0017 |
5 | NA18952.hp1 NA18982.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+547_128+548ins others(1): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779665 | |||||||
| chr2:38779665 | T | TATATA | 3 | a0001c0001t0002g0049 a0001c0001t0002g0057 a0001c0001t0024g0027 |
4 | HG01070.hp2 HG01071.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+547_128+548ins others(5): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779665 | |||||||
| chr2:38779665 | T | TATATATA | 5 | a0001c0001t0002g0020 a0001c0001t0002g0056 a0001c0001t0002g0058 others(2): Show |
6 | HG01943.hp2 HG01978.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+547_128+548ins others(7): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779665 | |||||||
| chr2:38779665 | T | TATATATA others(2): Show |
4 | a0001c0001t0002g0025 a0001c0001t0004g0045 a0001c0001t0004g0046 others(1): Show |
4 | HG01975.hp2 HG02630.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+547_128+548ins others(9): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779665 | |||||||
| chr2:38779665 | T | TATATATA others(4): Show |
2 | a0001c0001t0002g0053 a0001c0001t0005g0047 |
2 | HG01175.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.128+547_128+548ins others(11): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779665 | |||||||
| chr2:38779665 | T | TATATATA others(6): Show |
1 | a0001c0001t0002g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(13): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779665 | |||||||
| chr2:38779665 | T | TATATATA others(8): Show |
1 | a0001c0001t0005g0041 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.128+547_128+548ins others(15): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779665 | |||||||
| chr2:38779666 | T | A | 46 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0011 others(43): Show |
71 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.128+548T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779666 | |||||||
| chr2:38779667 | T | A | 15 | a0001c0001t0002g0020 a0001c0001t0002g0025 a0001c0001t0002g0038 others(12): Show |
17 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.128+549T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779667 | |||||||
| chr2:38779668 | T | A | 40 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0011 others(37): Show |
61 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.128+550T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779668 | |||||||
| chr2:38779669 | T | A | 13 | a0001c0001t0002g0020 a0001c0001t0002g0025 a0001c0001t0002g0038 others(10): Show |
15 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.128+551T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779669 | |||||||
| chr2:38779670 | T | A | 31 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0012 others(28): Show |
43 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.128+552T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779670 | |||||||
| chr2:38779671 | T | A | 8 | a0001c0001t0002g0025 a0001c0001t0002g0038 a0001c0001t0002g0049 others(5): Show |
9 | HG01070.hp2 HG01071.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.128+553T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779671 | |||||||
| chr2:38779672 | T | A | 13 | a0001c0001t0002g0011 a0001c0001t0002g0040 a0001c0001t0002g0048 others(10): Show |
15 | HG00280.hp1 HG01106.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.128+554T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779672 | |||||||
| chr2:38779673 | T | A | 5 | a0001c0001t0002g0025 a0001c0001t0002g0038 a0001c0001t0002g0049 others(2): Show |
5 | HG02630.hp2 HG02717.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+555T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779673 | |||||||
| chr2:38779674 | T | A | 5 | a0001c0001t0002g0040 a0001c0001t0002g0048 a0001c0001t0002g0053 others(2): Show |
5 | HG00280.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.128+556T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779674 | |||||||
| chr2:38779675 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.128+557T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779675 | |||||||
| chr2:38779680 | T | A | 1 | a0001c0001t0059g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.128+562T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779680 | |||||||
| chr2:38779682 | T | A | 1 | a0001c0001t0059g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.128+564T>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779682 | |||||||
| chr2:38779691 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG03209.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.128+573T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779691 | |||||||
| chr2:38779692 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.128+574C>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779692 | |||||||
| chr2:38779796 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.128+678C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779796 | |||||||
| chr2:38779816 | G | C | 6 | a0001c0001t0010g0017 a0001c0001t0010g0022 a0001c0001t0010g0065 others(3): Show |
9 | NA18952.hp1 NA18956.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.128+698G>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779816 | |||||||
| chr2:38779871 | C | T | 3 | a0001c0001t0008g0006 a0001c0001t0060g0006 a0001c0001t0061g0006 |
10 | NA18943.hp2 NA18946.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.128+753C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779871 | |||||||
| chr2:38779916 | C | A | 2 | a0001c0001t0001g0005 a0002c0002t0001g0005 |
11 | HG00408.hp2 NA18942.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.128+798C>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779916 | |||||||
| chr2:38779972 | C | T | 69 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 others(66): Show |
112 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.128+854C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38779972 | |||||||
| chr2:38780176 | C | T | 1 | a0001c0001t0011g0016 | 5 | HG02818.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+1058C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780176 | |||||||
| chr2:38780298 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.128+1180T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780298 | |||||||
| chr2:38780319 | C | CA | 10 | a0001c0001t0001g0030 a0001c0001t0001g0062 a0001c0001t0007g0077 others(7): Show |
12 | HG02015.hp2 HG02080.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.129-1185dupA | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38780319 | ||||||
| chr2:38780345 | G | C | 1 | a0001c0001t0027g0072 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.129-1172G>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780345 | |||||||
| chr2:38780390 | A | T | 1 | a0001c0001t0042g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.129-1127A>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780390 | |||||||
| chr2:38780391 | G | A | 1 | a0001c0001t0059g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.129-1126G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780391 | |||||||
| chr2:38780426 | G | A | 1 | a0001c0001t0025g0031 | 2 | HG00642.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.129-1091G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780426 | |||||||
| chr2:38780512 | GTATTTTT others(282): Show |
G | 1 | a0001c0001t0004g0046 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.129-972_129-684del | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38780512 | ||||||
| chr2:38780636 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.129-881C>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780636 | |||||||
| chr2:38780636 | C | CA | 3 | a0001c0001t0002g0013 a0001c0001t0002g0057 a0001c0001t0005g0013 |
4 | HG00735.hp2 HG01168.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-881_129-880ins others(1): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780636 | |||||||
| chr2:38780655 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0020g0008 a0001c0001t0039g0008 |
8 | HG01891.hp1 HG02486.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-862G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780655 | |||||||
| chr2:38780665 | G | T | 7 | a0001c0001t0010g0017 a0001c0001t0010g0022 a0001c0001t0010g0065 others(4): Show |
10 | HG02886.hp2 NA18952.hp1 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.129-852G>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780665 | |||||||
| chr2:38780680 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(52): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.129-837G>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780680 | |||||||
| chr2:38780767 | T | C | 65 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 others(62): Show |
104 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.129-750T>C | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780767 | |||||||
| chr2:38780801 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.129-716A>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780801 | |||||||
| chr2:38780932 | T | G | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.129-585T>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38780932 | |||||||
| chr2:38780970 | CCTT | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(42): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.129-540_129-538del others(3): Show |
GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr2 | 38780970 | ||||||
| chr2:38781000 | A | G | 8 | a0001c0001t0010g0017 a0001c0001t0010g0022 a0001c0001t0010g0065 others(5): Show |
11 | HG02559.hp1 HG02886.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.129-517A>G | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38781000 | |||||||
| chr2:38781212 | C | A | 1 | a0002c0002t0001g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.129-305C>A | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38781212 | |||||||
| chr2:38781319 | C | T | 1 | a0001c0001t0031g0066 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.129-198C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38781319 | |||||||
| chr2:38781326 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(50): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.129-191C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38781326 | |||||||
| chr2:38781441 | C | T | 2 | a0001c0001t0017g0076 a0001c0001t0017g0083 |
2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.129-76C>T | GEMIN6 | ENSG00000152147.11 | transcript | ENST00000281950.8 | protein_coding | 2/2 | chr2 | 38781441 |