Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25853 |
| ensemblid | ENSG00000198876.13 |
| hgncid | 19911 |
| symbol | DCAF12 |
| name | DDB1 and CUL4 associated factor 12 |
| refseq_nuc | NM_015397.4 |
| refseq_prot | NP_056212.1 |
| ensembl_nuc | ENST00000361264.9 |
| ensembl_prot | ENSP00000355114.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 34086387 |
| end | 34126698 |
| strand | - |
| ver | v1.2 |
| region | chr9:34086387-34126698 |
| region5000 | chr9:34081387-34131698 |
| regionname0 | DCAF12_chr9_34086387_34126698 |
| regionname5000 | DCAF12_chr9_34081387_34131698 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 453 | 280 | 94 | 59 | 76 | 15 | 34 | 54 | DCAF12_chr9_34081387_34131698 | DCAF12 | MARKV others(448): Show |
chr9 | 34081387 | 34131698 |
| a0002 | 0/0 | 453 | 89 | 1 | 21 | 52 | 3 | 12 | 36 | DCAF12_chr9_34081387_34131698 | DCAF12 | MARKV others(448): Show |
chr9 | 34081387 | 34131698 |
| a0003 | 0/0 | 453 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | MARKV others(448): Show |
chr9 | 34081387 | 34131698 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1359 | 264 | 93 | 54 | 75 | 9 | 31 | DCAF12_chr9_34081387_34131698 | DCAF12 | ATGGC others(1354): Show |
chr9 | 34081387 | 34131698 | ||
| a0001c0003 | 0/0 | 1359 | 14 | 1 | 4 | 0 | 6 | 3 | DCAF12_chr9_34081387_34131698 | DCAF12 | ATGGC others(1354): Show |
chr9 | 34081387 | 34131698 | ||
| a0001c0004 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | ATGGC others(1354): Show |
chr9 | 34081387 | 34131698 | ||
| a0001c0006 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | ATGGC others(1354): Show |
chr9 | 34081387 | 34131698 | ||
| a0002c0002 | 0/0 | 1359 | 89 | 1 | 21 | 52 | 3 | 12 | DCAF12_chr9_34081387_34131698 | DCAF12 | ATGGC others(1354): Show |
chr9 | 34081387 | 34131698 | ||
| a0003c0005 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | ATGGC others(1354): Show |
chr9 | 34081387 | 34131698 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3597 | 124 | 26 | 26 | 45 | 8 | 18 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0002 | 0/0 | 3597 | 40 | 32 | 6 | 1 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0003 | 1/0 | 3592 | 47 | 7 | 7 | 28 | 0 | 4 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3587): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0004 | 0/0 | 3597 | 34 | 20 | 10 | 0 | 1 | 3 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0007 | 0/0 | 3592 | 4 | 1 | 2 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3587): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0008 | 0/0 | 3594 | 4 | 4 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3589): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0011 | 0/0 | 3597 | 2 | 0 | 0 | 0 | 0 | 2 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0012 | 0/0 | 3592 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3587): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0013 | 0/0 | 3592 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3587): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0014 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0015 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0016 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0017 | 0/0 | 3597 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0018 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0019 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0001t0020 | 0/0 | 3592 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3587): Show |
chr9 | 34081387 | 34131698 |
| a0001c0003t0001 | 0/0 | 3597 | 11 | 0 | 4 | 0 | 4 | 3 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0003t0009 | 0/0 | 3597 | 3 | 1 | 0 | 0 | 2 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0004t0001 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0001c0006t0002 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0002c0002t0002 | 0/0 | 3597 | 72 | 1 | 14 | 46 | 3 | 8 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0002c0002t0003 | 0/0 | 3592 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3587): Show |
chr9 | 34081387 | 34131698 |
| a0002c0002t0005 | 0/0 | 3597 | 8 | 0 | 4 | 0 | 0 | 4 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0002c0002t0006 | 0/0 | 3597 | 5 | 0 | 3 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0002c0002t0010 | 0/0 | 3597 | 3 | 0 | 0 | 3 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| a0003c0005t0004 | 0/0 | 3597 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | GTTCT others(3592): Show |
chr9 | 34081387 | 34131698 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0011g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0011g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0012g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0013g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0015g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0016g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0017g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0019g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0001t0020g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0009g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0003t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0004t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0001c0006t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0002 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0006g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0006g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0002c0002t0010g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| a0003c0005t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0001 | g0077 | EUR | GBR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0215 | EUR | GBR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00140 | hp1 | a0001 | c0003 | t0009 | g0085 | EUR | GBR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | FIN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0233 | EUR | FIN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00639 | hp1 | a0002 | c0002 | t0005 | g0258 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0185 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0312 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0274 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0078 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG00738 | hp2 | a0002 | c0002 | t0005 | g0275 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0178 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0177 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0304 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0226 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01168 | hp1 | a0002 | c0002 | t0005 | g0223 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0295 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01169 | hp1 | a0002 | c0002 | t0005 | g0256 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0305 | AMR | PUR | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0327 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0316 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01257 | hp1 | a0001 | c0004 | t0001 | g0025 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01261 | hp1 | a0002 | c0002 | t0006 | g0210 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0196 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01433 | hp2 | a0001 | c0001 | t0015 | g0120 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01515 | hp2 | a0001 | c0003 | t0009 | g0086 | EUR | IBS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0079 | EUR | IBS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0011 | EUR | IBS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01928 | hp1 | a0002 | c0002 | t0006 | g0192 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0307 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01952 | hp1 | a0001 | c0001 | t0013 | g0096 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01975 | hp2 | a0001 | c0003 | t0001 | g0081 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01978 | hp2 | a0001 | c0001 | t0019 | g0337 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0260 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0335 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0308 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0323 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02055 | hp1 | a0001 | c0001 | t0014 | g0031 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0237 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02145 | hp1 | a0001 | c0003 | t0009 | g0087 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0319 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0334 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CDX | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | CDX | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0317 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0180 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02293 | hp1 | a0002 | c0002 | t0006 | g0217 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0142 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0221 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0083 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02683 | hp1 | a0001 | c0001 | t0017 | g0047 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0251 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0028 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0297 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0175 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03490 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0084 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0303 | AFR | GWD | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03688 | hp1 | a0002 | c0002 | t0005 | g0255 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0012 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0310 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0034 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0155 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0193 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0207 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0245 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0259 | SAS | BEB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0033 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04199 | hp2 | a0002 | c0002 | t0005 | g0321 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0179 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04204 | hp2 | a0002 | c0002 | t0005 | g0257 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | YRI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | YRI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0238 | AFR | YRI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0324 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18957 | hp2 | a0002 | c0002 | t0003 | g0227 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18960 | hp2 | a0002 | c0002 | t0010 | g0216 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0254 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18970 | hp1 | a0002 | c0002 | t0006 | g0018 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18975 | hp1 | a0002 | c0002 | t0010 | g0209 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0239 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18980 | hp2 | a0002 | c0002 | t0010 | g0212 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19011 | hp1 | a0001 | c0001 | t0020 | g0338 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0283 | AFR | LWK | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0285 | AFR | LWK | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | LWK | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19063 | hp1 | a0001 | c0006 | t0002 | g0332 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0326 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19085 | hp1 | a0002 | c0002 | t0006 | g0018 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0029 | AFR | YRI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ASW | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | ASW | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0289 | EUR | TSI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0080 | EUR | TSI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0272 | EUR | TSI | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | GIH | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20905 | hp2 | a0002 | c0002 | t0005 | g0320 | SAS | GIH | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0288 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0290 | AMR | CLM | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0309 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02559 | hp1 | a0003 | c0005 | t0004 | g0301 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0246 | AFR | ACB | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | MSL | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0281 | AFR | USA | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | USA | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0230 | AFR | USA | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | LWK | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0127 | REF | REF | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0247 | REF | REF | DCAF12_chr9_34081387_34131698 | DCAF12 | chr9 | 34081387 | 34131698 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34089516 | T | A | 1 | a0003 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1099A>T | p.Ile367Phe | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/9 | 1366/3592 | 1099/1362 | 367/453 | chr9 | 34089516 | |||
| chr9:34107507 | C | T | 1 | a0002 | 89 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
missense_variant | MODERATE | c.392G>A | p.Arg131Gln | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/9 | 659/3592 | 392/1362 | 131/453 | chr9 | 34107507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34106453 | G | A | 1 | a0001c0006 | 1 | NA19063.hp1 | synonymous_variant | LOW | c.582C>T | p.Ser194Ser | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/9 | 849/3592 | 582/1362 | 194/453 | chr9 | 34106453 | |||
| chr9:34107506 | C | T | 1 | a0001c0003 | 14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
synonymous_variant | LOW | c.393G>A | p.Arg131Arg | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/9 | 660/3592 | 393/1362 | 131/453 | chr9 | 34107506 | |||
| chr9:34125260 | C | G | 1 | a0001c0004 | 1 | HG01257.hp1 | synonymous_variant | LOW | c.96G>C | p.Ser32Ser | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/9 | 363/3592 | 96/1362 | 32/453 | chr9 | 34125260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34086492 | G | C | 1 | a0001c0001t0015 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1858C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 1858 | chr9 | 34086492 | ||||||
| chr9:34086579 | T | A | 1 | a0001c0001t0014 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1771A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 1771 | chr9 | 34086579 | ||||||
| chr9:34086762 | C | T | 1 | a0002c0002t0006 | 5 | HG01261.hp1 HG01928.hp1 HG02293.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1588G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 1588 | chr9 | 34086762 | ||||||
| chr9:34086861 | C | G | 1 | a0002c0002t0010 | 3 | NA18960.hp2 NA18975.hp1 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1489G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 1489 | chr9 | 34086861 | ||||||
| chr9:34087147 | C | T | 1 | a0001c0001t0012 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1203G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 1203 | chr9 | 34087147 | ||||||
| chr9:34087248 | C | T | 3 | a0001c0001t0004 a0001c0001t0014 a0003c0005t0004 |
36 | HG00735.hp1 HG01074.hp2 HG01123.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1102G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 1102 | chr9 | 34087248 | ||||||
| chr9:34087256 | C | G | 1 | a0001c0001t0011 | 2 | HG03831.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1094G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 1094 | chr9 | 34087256 | ||||||
| chr9:34087362 | T | C | 13 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(10): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
3_prime_UTR_variant | MODIFIER | c.*988A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 988 | chr9 | 34087362 | ||||||
| chr9:34087535 | G | A | 1 | a0001c0001t0007 | 4 | HG01069.hp1 HG01071.hp2 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*815C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 815 | chr9 | 34087535 | ||||||
| chr9:34087537 | G | A | 1 | a0001c0001t0016 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 813 | chr9 | 34087537 | ||||||
| chr9:34087564 | G | C | 1 | a0001c0001t0017 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*786C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 786 | chr9 | 34087564 | ||||||
| chr9:34087632 | A | G | 1 | a0001c0003t0009 | 3 | HG00140.hp1 HG01515.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*718T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 718 | chr9 | 34087632 | ||||||
| chr9:34087784 | T | C | 1 | a0002c0002t0005 | 8 | HG00639.hp1 HG00738.hp2 HG01168.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*566A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 566 | chr9 | 34087784 | ||||||
| chr9:34088024 | G | GAAAGA | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(17): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*325_*326insTCTTT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 325 | chr9 | 34088024 | ||||||
| chr9:34088098 | CAAT | C | 1 | a0001c0001t0008 | 4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*249_*251delATT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 249 | chr9 | 34088098 | ||||||
| chr9:34088181 | T | C | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*169A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 9/9 | 169 | chr9 | 34088181 | ||||||
| chr9:34126489 | C | A | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-58G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 58 | chr9 | 34126489 | ||||||
| chr9:34126490 | A | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 59 | chr9 | 34126490 | ||||||
| chr9:34126491 | G | A | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-60C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | chr9 | 34126491 | |||||||
| chr9:34126492 | G | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 61 | chr9 | 34126492 | ||||||
| chr9:34126500 | G | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 69 | chr9 | 34126500 | ||||||
| chr9:34126502 | C | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 71 | chr9 | 34126502 | ||||||
| chr9:34126503 | A | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 72 | chr9 | 34126503 | ||||||
| chr9:34126504 | T | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-73A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | chr9 | 34126504 | |||||||
| chr9:34126505 | A | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-74T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 74 | chr9 | 34126505 | ||||||
| chr9:34126506 | T | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 75 | chr9 | 34126506 | ||||||
| chr9:34126507 | A | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 76 | chr9 | 34126507 | ||||||
| chr9:34126509 | T | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-78A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 78 | chr9 | 34126509 | ||||||
| chr9:34126511 | G | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 80 | chr9 | 34126511 | ||||||
| chr9:34126512 | G | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 81 | chr9 | 34126512 | ||||||
| chr9:34126518 | G | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-87C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 87 | chr9 | 34126518 | ||||||
| chr9:34126522 | C | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-91G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 91 | chr9 | 34126522 | ||||||
| chr9:34126526 | C | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 95 | chr9 | 34126526 | ||||||
| chr9:34126527 | A | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 96 | chr9 | 34126527 | ||||||
| chr9:34126528 | C | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-97G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | chr9 | 34126528 | |||||||
| chr9:34126530 | T | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-99A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 99 | chr9 | 34126530 | ||||||
| chr9:34126531 | T | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-100A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 100 | chr9 | 34126531 | ||||||
| chr9:34126532 | A | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 101 | chr9 | 34126532 | ||||||
| chr9:34126534 | T | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-103A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 103 | chr9 | 34126534 | ||||||
| chr9:34126535 | G | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-104C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 104 | chr9 | 34126535 | ||||||
| chr9:34126536 | C | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 105 | chr9 | 34126536 | ||||||
| chr9:34126539 | C | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 108 | chr9 | 34126539 | ||||||
| chr9:34126541 | G | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 110 | chr9 | 34126541 | ||||||
| chr9:34126549 | A | C | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-118T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | chr9 | 34126549 | |||||||
| chr9:34126550 | A | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-119T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 119 | chr9 | 34126550 | ||||||
| chr9:34126561 | C | A | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 130 | chr9 | 34126561 | ||||||
| chr9:34126562 | C | G | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 131 | chr9 | 34126562 | ||||||
| chr9:34126563 | C | T | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 132 | chr9 | 34126563 | ||||||
| chr9:34126564 | G | A | 1 | a0001c0001t0019 | 1 | HG01978.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-133C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | chr9 | 34126564 | |||||||
| chr9:34126595 | G | A | 1 | a0001c0001t0020 | 1 | NA19011.hp1 | 5_prime_UTR_variant | MODIFIER | c.-164C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/9 | 164 | chr9 | 34126595 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:34088563 | G | C | 17 | a0001c0001t0004g0155 a0001c0001t0004g0190 a0001c0001t0004g0191 others(14): Show |
17 | HG00735.hp1 HG01123.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1204-55C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34088563 | |||||||
| chr9:34088655 | C | T | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-147G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34088655 | |||||||
| chr9:34088660 | G | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0286 others(2): Show |
5 | HG01109.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204-152C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34088660 | |||||||
| chr9:34088703 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1204-195G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34088703 | |||||||
| chr9:34088835 | C | T | 1 | a0001c0001t0003g0278 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1204-327G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34088835 | |||||||
| chr9:34088922 | C | A | 1 | a0001c0001t0002g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1204-414G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34088922 | |||||||
| chr9:34088953 | A | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1204-445T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34088953 | |||||||
| chr9:34089110 | C | CA | 21 | a0001c0001t0001g0035 a0001c0001t0002g0004 a0001c0001t0002g0163 others(18): Show |
23 | HG00438.hp1 HG00438.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1203+301dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34089110 | |||||||
| chr9:34089110 | CA | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(74): Show |
82 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1203+301delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34089110 | |||||||
| chr9:34089110 | CAA | C | 6 | a0001c0001t0001g0110 a0001c0001t0001g0139 a0001c0001t0008g0029 others(3): Show |
6 | HG02015.hp2 HG02630.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1203+300_1203+301d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34089110 | |||||||
| chr9:34089267 | C | T | 2 | a0001c0001t0002g0163 a0001c0001t0002g0181 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1203+145G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34089267 | |||||||
| chr9:34089277 | C | A | 1 | a0002c0002t0005g0320 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1203+135G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34089277 | |||||||
| chr9:34089352 | T | C | 2 | a0001c0001t0008g0029 a0001c0001t0008g0030 |
2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1203+60A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34089352 | |||||||
| chr9:34089397 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1203+15A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 8/8 | chr9 | 34089397 | |||||||
| chr9:34089737 | A | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1025-147T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34089737 | |||||||
| chr9:34089875 | A | G | 1 | a0002c0002t0002g0230 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1025-285T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34089875 | |||||||
| chr9:34090124 | C | T | 23 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0002g0293 others(20): Show |
23 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1025-534G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34090124 | |||||||
| chr9:34090159 | G | A | 1 | a0001c0001t0003g0162 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1025-569C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34090159 | |||||||
| chr9:34090649 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1025-1059C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34090649 | |||||||
| chr9:34090674 | C | CT | 6 | a0002c0002t0002g0165 a0002c0002t0002g0211 a0002c0002t0002g0225 others(3): Show |
6 | HG00558.hp2 HG04184.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-1085dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34090674 | |||||||
| chr9:34090803 | C | T | 1 | a0001c0001t0004g0306 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1025-1213G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34090803 | |||||||
| chr9:34090940 | C | G | 7 | a0001c0001t0004g0020 a0001c0001t0004g0284 a0001c0001t0004g0285 others(4): Show |
8 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1025-1350G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34090940 | |||||||
| chr9:34091271 | G | T | 1 | a0002c0002t0010g0209 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1025-1681C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091271 | |||||||
| chr9:34091340 | C | A | 4 | a0001c0001t0003g0156 a0001c0001t0003g0168 a0001c0001t0003g0202 others(1): Show |
4 | HG00642.hp1 HG00733.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025-1750G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091340 | |||||||
| chr9:34091419 | G | T | 1 | a0001c0001t0004g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1025-1829C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091419 | |||||||
| chr9:34091422 | G | T | 1 | a0001c0001t0004g0298 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1025-1832C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091422 | |||||||
| chr9:34091423 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1025-1833A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091423 | |||||||
| chr9:34091466 | G | A | 43 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0002g0291 others(40): Show |
44 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.1024+1820C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091466 | |||||||
| chr9:34091527 | T | C | 1 | a0002c0002t0002g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1024+1759A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091527 | |||||||
| chr9:34091639 | C | CA | 102 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(99): Show |
107 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1024+1646dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091639 | |||||||
| chr9:34091639 | C | CAA | 17 | a0001c0001t0001g0010 a0001c0001t0001g0049 a0001c0001t0001g0054 others(14): Show |
18 | HG01106.hp2 HG01123.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1024+1645_1024+164 others(6): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091639 | |||||||
| chr9:34091639 | C | CAAA | 59 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0088 others(56): Show |
64 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1024+1644_1024+164 others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091639 | |||||||
| chr9:34091639 | C | CAAAA | 14 | a0001c0001t0001g0091 a0001c0001t0001g0100 a0001c0001t0001g0106 others(11): Show |
14 | HG00408.hp2 HG01358.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1024+1643_1024+164 others(8): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091639 | |||||||
| chr9:34091639 | C | CAAAAA | 10 | a0001c0001t0001g0149 a0001c0003t0001g0011 a0001c0003t0001g0027 others(7): Show |
11 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1024+1642_1024+164 others(9): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091639 | |||||||
| chr9:34091639 | CA | C | 6 | a0001c0001t0002g0163 a0001c0001t0002g0181 a0001c0001t0003g0266 others(3): Show |
6 | HG01993.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024+1646delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091639 | |||||||
| chr9:34091661 | A | C | 2 | a0001c0001t0003g0330 a0001c0001t0003g0331 |
2 | NA18961.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1024+1625T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091661 | |||||||
| chr9:34091662 | C | A | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1624G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091662 | |||||||
| chr9:34091671 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1024+1615T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091671 | |||||||
| chr9:34091675 | A | C | 3 | a0002c0002t0010g0209 a0002c0002t0010g0212 a0002c0002t0010g0216 |
3 | NA18960.hp2 NA18975.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1024+1611T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34091675 | |||||||
| chr9:34092256 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1024+1030T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092256 | |||||||
| chr9:34092339 | A | G | 1 | a0001c0001t0004g0284 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1024+947T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092339 | |||||||
| chr9:34092398 | G | A | 2 | a0001c0001t0008g0029 a0001c0001t0008g0030 |
2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1024+888C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092398 | |||||||
| chr9:34092427 | C | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1024+859G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092427 | |||||||
| chr9:34092427 | C | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1024+859G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092427 | |||||||
| chr9:34092432 | A | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
95 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.1024+854T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092432 | |||||||
| chr9:34092642 | C | G | 2 | a0002c0002t0002g0195 a0002c0002t0002g0196 |
2 | HG01256.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1024+644G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092642 | |||||||
| chr9:34092660 | T | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1024+626A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092660 | |||||||
| chr9:34092684 | C | CA | 28 | a0001c0001t0001g0060 a0001c0001t0004g0190 a0001c0001t0004g0287 others(25): Show |
29 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.1024+601dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092684 | |||||||
| chr9:34092694 | A | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0040 others(91): Show |
102 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1024+592T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092694 | |||||||
| chr9:34092709 | A | C | 2 | a0001c0001t0001g0060 a0002c0002t0002g0214 |
2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1024+577T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092709 | |||||||
| chr9:34092779 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1024+507T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092779 | |||||||
| chr9:34092922 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 |
3 | HG02451.hp1 HG03209.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1024+364G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092922 | |||||||
| chr9:34092970 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.1024+316A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092970 | |||||||
| chr9:34092972 | A | C | 3 | a0001c0001t0007g0177 a0001c0001t0007g0178 a0001c0001t0007g0180 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1024+314T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092972 | |||||||
| chr9:34092974 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(176): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1024+312G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092974 | |||||||
| chr9:34092993 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1024+293C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34092993 | |||||||
| chr9:34093017 | G | T | 1 | a0001c0001t0004g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1024+269C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34093017 | |||||||
| chr9:34093092 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(176): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1024+194T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34093092 | |||||||
| chr9:34093101 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1024+185C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34093101 | |||||||
| chr9:34093258 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1024+28C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34093258 | |||||||
| chr9:34093276 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1024+10C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 7/8 | chr9 | 34093276 | |||||||
| chr9:34093519 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.862-71G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34093519 | |||||||
| chr9:34093971 | G | C | 1 | a0002c0002t0002g0250 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.862-523C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34093971 | |||||||
| chr9:34094009 | A | G | 1 | a0001c0001t0004g0288 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.862-561T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094009 | |||||||
| chr9:34094130 | C | G | 10 | a0002c0002t0002g0012 a0002c0002t0002g0022 a0002c0002t0002g0207 others(7): Show |
11 | HG02027.hp1 HG03704.hp2 HG04115.hp2 others(8): Show |
intron_variant | MODIFIER | c.862-682G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094130 | |||||||
| chr9:34094131 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.862-683C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094131 | |||||||
| chr9:34094531 | C | CT | 16 | a0001c0001t0001g0049 a0001c0001t0001g0065 a0001c0001t0001g0068 others(13): Show |
16 | HG00621.hp1 HG01106.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.862-1084dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094531 | |||||||
| chr9:34094580 | G | C | 1 | a0002c0002t0002g0239 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.862-1132C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094580 | |||||||
| chr9:34094584 | A | G | 2 | a0002c0002t0002g0214 a0002c0002t0002g0215 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.862-1136T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094584 | |||||||
| chr9:34094592 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.862-1144C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094592 | |||||||
| chr9:34094653 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0102 a0001c0001t0001g0104 |
3 | NA18950.hp2 NA18963.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.862-1205G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094653 | |||||||
| chr9:34094685 | C | T | 1 | a0002c0002t0005g0321 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.862-1237G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094685 | |||||||
| chr9:34094720 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.862-1272G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094720 | |||||||
| chr9:34094724 | G | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0182 a0001c0001t0002g0183 others(1): Show |
6 | HG01175.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.862-1276C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094724 | |||||||
| chr9:34094738 | G | C | 4 | a0001c0001t0004g0299 a0001c0001t0004g0304 a0001c0001t0004g0309 others(1): Show |
4 | HG01074.hp2 HG01255.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.862-1290C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094738 | |||||||
| chr9:34094793 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0064 others(4): Show |
7 | HG01496.hp1 HG02109.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.862-1345C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094793 | |||||||
| chr9:34094809 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.862-1361G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094809 | |||||||
| chr9:34094822 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.862-1374T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094822 | |||||||
| chr9:34094832 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.862-1384C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094832 | |||||||
| chr9:34094868 | T | C | 12 | a0002c0002t0002g0012 a0002c0002t0002g0022 a0002c0002t0002g0151 others(9): Show |
13 | HG02027.hp1 HG03669.hp1 HG03704.hp2 others(10): Show |
intron_variant | MODIFIER | c.862-1420A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094868 | |||||||
| chr9:34094903 | T | C | 1 | a0001c0001t0003g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.862-1455A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34094903 | |||||||
| chr9:34095024 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.862-1576A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095024 | |||||||
| chr9:34095083 | CT | C | 154 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(151): Show |
175 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.861+1632delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095083 | |||||||
| chr9:34095108 | C | T | 1 | a0001c0001t0007g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.861+1608G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095108 | |||||||
| chr9:34095140 | T | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.861+1576A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095140 | |||||||
| chr9:34095169 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.861+1547C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095169 | |||||||
| chr9:34095199 | C | T | 4 | a0001c0001t0002g0164 a0001c0001t0002g0170 a0001c0001t0002g0171 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.861+1517G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095199 | |||||||
| chr9:34095363 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.861+1353C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095363 | |||||||
| chr9:34095372 | C | CT | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
101 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.861+1343dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095372 | |||||||
| chr9:34095372 | C | CTT | 18 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0049 others(15): Show |
18 | HG00609.hp2 HG01106.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.861+1342_861+1343d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095372 | |||||||
| chr9:34095372 | CT | C | 9 | a0001c0001t0002g0261 a0001c0001t0002g0263 a0001c0001t0002g0282 others(6): Show |
9 | HG01069.hp1 HG01109.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.861+1343delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095372 | |||||||
| chr9:34095372 | CTTTTT | C | 12 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(9): Show |
13 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.861+1339_861+1343d others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095372 | |||||||
| chr9:34095372 | CTTTTTTT others(2): Show |
C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(66): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.861+1335_861+1343d others(11): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095372 | |||||||
| chr9:34095508 | C | G | 5 | a0001c0001t0004g0298 a0001c0001t0004g0302 a0001c0001t0004g0303 others(2): Show |
5 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.861+1208G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095508 | |||||||
| chr9:34095719 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(281): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.861+997G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095719 | |||||||
| chr9:34095739 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.861+977T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095739 | |||||||
| chr9:34095816 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.861+900C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095816 | |||||||
| chr9:34095828 | C | T | 1 | a0002c0002t0005g0257 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.861+888G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095828 | |||||||
| chr9:34095998 | C | A | 1 | a0001c0001t0002g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.861+718G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34095998 | |||||||
| chr9:34096061 | A | C | 1 | a0001c0001t0001g0149 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.861+655T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34096061 | |||||||
| chr9:34096599 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(176): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.861+117C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34096599 | |||||||
| chr9:34096608 | A | G | 1 | a0002c0002t0002g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.861+108T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 6/8 | chr9 | 34096608 | |||||||
| chr9:34096875 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.796-94A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34096875 | |||||||
| chr9:34097063 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.796-282A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097063 | |||||||
| chr9:34097256 | C | CT | 29 | a0001c0001t0001g0053 a0001c0001t0001g0066 a0001c0001t0002g0164 others(26): Show |
29 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.796-476dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097256 | |||||||
| chr9:34097256 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0050 a0001c0001t0001g0055 others(77): Show |
86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.796-476delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097256 | |||||||
| chr9:34097331 | G | A | 1 | a0001c0003t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.796-550C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097331 | |||||||
| chr9:34097559 | ACT | A | 5 | a0001c0001t0004g0298 a0001c0001t0004g0302 a0001c0001t0004g0303 others(2): Show |
5 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.795+763_795+764del others(2): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097559 | |||||||
| chr9:34097604 | T | C | 1 | a0003c0005t0004g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.795+720A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097604 | |||||||
| chr9:34097641 | A | G | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+683T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097641 | |||||||
| chr9:34097670 | C | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0123 others(1): Show |
4 | HG02258.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+654G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097670 | |||||||
| chr9:34097798 | C | T | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0286 others(2): Show |
5 | HG01109.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.795+526G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097798 | |||||||
| chr9:34097887 | C | T | 6 | a0002c0002t0002g0165 a0002c0002t0002g0211 a0002c0002t0002g0225 others(3): Show |
6 | HG00558.hp2 HG04184.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.795+437G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097887 | |||||||
| chr9:34097939 | G | GA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(68): Show |
76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.795+384dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097939 | |||||||
| chr9:34097961 | A | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0182 a0001c0001t0002g0183 others(2): Show |
7 | HG01175.hp2 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.795+363T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34097961 | |||||||
| chr9:34098112 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(186): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.795+212A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34098112 | |||||||
| chr9:34098259 | G | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.795+65C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 5/8 | chr9 | 34098259 | |||||||
| chr9:34098655 | C | T | 1 | a0001c0001t0003g0265 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.602-138G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34098655 | |||||||
| chr9:34098777 | A | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.602-260T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34098777 | |||||||
| chr9:34098871 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.602-354G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34098871 | |||||||
| chr9:34099008 | G | A | 1 | a0002c0002t0005g0257 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.602-491C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099008 | |||||||
| chr9:34099072 | C | CT | 15 | a0001c0001t0001g0137 a0001c0001t0003g0186 a0001c0003t0001g0011 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.602-556dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099072 | |||||||
| chr9:34099099 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0145 |
3 | HG02965.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.602-582C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099099 | |||||||
| chr9:34099216 | T | C | 1 | a0003c0005t0004g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.602-699A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099216 | |||||||
| chr9:34099313 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.602-796A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099313 | |||||||
| chr9:34099523 | C | T | 1 | a0002c0002t0002g0324 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.602-1006G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099523 | |||||||
| chr9:34099586 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.602-1069T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099586 | |||||||
| chr9:34099592 | C | CT | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.602-1076dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099592 | |||||||
| chr9:34099696 | C | G | 1 | a0002c0002t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.602-1179G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34099696 | |||||||
| chr9:34100034 | T | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.602-1517A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100034 | |||||||
| chr9:34100072 | C | G | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.602-1555G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100072 | |||||||
| chr9:34100198 | C | CT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(84): Show |
92 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.602-1682dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100198 | |||||||
| chr9:34100198 | CT | C | 8 | a0001c0001t0001g0035 a0001c0001t0002g0164 a0001c0001t0002g0170 others(5): Show |
8 | HG02451.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-1682delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100198 | |||||||
| chr9:34100238 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.602-1721C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100238 | |||||||
| chr9:34100433 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.602-1916G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100433 | |||||||
| chr9:34100476 | G | A | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-1959C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100476 | |||||||
| chr9:34100499 | C | CT | 15 | a0001c0001t0001g0131 a0001c0001t0014g0031 a0001c0003t0001g0011 others(12): Show |
16 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-1983dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100499 | |||||||
| chr9:34100620 | G | A | 4 | a0001c0001t0004g0299 a0001c0001t0004g0304 a0001c0001t0004g0309 others(1): Show |
4 | HG01074.hp2 HG01255.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-2103C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100620 | |||||||
| chr9:34100669 | A | AT | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.602-2153dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100669 | |||||||
| chr9:34100669 | AT | A | 6 | a0001c0001t0002g0166 a0001c0001t0004g0298 a0001c0001t0004g0302 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-2153delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100669 | |||||||
| chr9:34100676 | T | C | 3 | a0001c0001t0002g0325 a0002c0002t0002g0021 a0002c0002t0002g0324 |
4 | HG02155.hp1 NA18941.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-2159A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100676 | |||||||
| chr9:34100811 | A | AT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.602-2295dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100811 | |||||||
| chr9:34100868 | G | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.602-2351C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100868 | |||||||
| chr9:34100919 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.602-2402T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34100919 | |||||||
| chr9:34101064 | C | CT | 225 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(222): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.602-2548dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101064 | |||||||
| chr9:34101064 | C | CTT | 78 | a0001c0001t0001g0048 a0001c0001t0002g0003 a0001c0001t0002g0164 others(75): Show |
85 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.602-2549_602-2548d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101064 | |||||||
| chr9:34101064 | CT | C | 8 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0286 others(5): Show |
8 | HG00738.hp1 HG01109.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-2548delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101064 | |||||||
| chr9:34101103 | G | A | 19 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0002g0293 others(16): Show |
19 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.602-2586C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101103 | |||||||
| chr9:34101131 | A | C | 1 | a0001c0001t0004g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.602-2614T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101131 | |||||||
| chr9:34101332 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-2815G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101332 | |||||||
| chr9:34101333 | G | A | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-2816C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101333 | |||||||
| chr9:34101377 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.602-2860A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101377 | |||||||
| chr9:34101592 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(86): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.602-3075T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101592 | |||||||
| chr9:34101688 | G | A | 3 | a0002c0002t0002g0194 a0002c0002t0002g0228 a0002c0002t0002g0229 |
3 | NA18946.hp1 NA18994.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.602-3171C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101688 | |||||||
| chr9:34101780 | T | TGA | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-3265_602-3264d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101780 | |||||||
| chr9:34101810 | T | C | 1 | a0001c0001t0003g0162 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.602-3293A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101810 | |||||||
| chr9:34101977 | C | T | 10 | a0001c0001t0003g0156 a0001c0001t0003g0168 a0001c0001t0003g0202 others(7): Show |
10 | HG00642.hp1 HG00733.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.602-3460G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34101977 | |||||||
| chr9:34102014 | C | CA | 7 | a0001c0001t0001g0042 a0001c0001t0001g0073 a0001c0001t0002g0157 others(4): Show |
7 | HG01884.hp1 HG02280.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.602-3498dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102014 | |||||||
| chr9:34102014 | CA | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.602-3498delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102014 | |||||||
| chr9:34102098 | C | CG | 6 | a0001c0001t0001g0136 a0001c0001t0003g0204 a0001c0001t0014g0031 others(3): Show |
6 | HG01175.hp1 HG01928.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-3582dupC | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102098 | |||||||
| chr9:34102182 | G | A | 6 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 others(3): Show |
6 | HG00738.hp1 HG01975.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-3665C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102182 | |||||||
| chr9:34102211 | C | G | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-3694G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102211 | |||||||
| chr9:34102236 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.602-3719C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102236 | |||||||
| chr9:34102283 | C | CA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.602-3767dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102283 | |||||||
| chr9:34102477 | A | G | 1 | a0001c0001t0003g0265 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.601+3957T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102477 | |||||||
| chr9:34102602 | G | A | 1 | a0002c0002t0002g0326 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.601+3832C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102602 | |||||||
| chr9:34102666 | A | AAACAAC | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.601+3762_601+3767d others(8): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102666 | |||||||
| chr9:34102723 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+3711C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102723 | |||||||
| chr9:34102749 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.601+3685A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102749 | |||||||
| chr9:34102813 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.601+3621G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102813 | |||||||
| chr9:34102857 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.601+3577G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102857 | |||||||
| chr9:34102893 | T | C | 1 | a0001c0001t0004g0288 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601+3541A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102893 | |||||||
| chr9:34102975 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.601+3459T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34102975 | |||||||
| chr9:34103003 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.601+3431A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103003 | |||||||
| chr9:34103041 | GATCAC | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.601+3388_601+3392d others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103041 | |||||||
| chr9:34103052 | G | A | 2 | a0001c0001t0008g0083 a0001c0001t0008g0084 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.601+3382C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103052 | |||||||
| chr9:34103095 | C | CA | 28 | a0001c0001t0002g0173 a0001c0001t0002g0175 a0001c0001t0002g0243 others(25): Show |
29 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.601+3338dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103095 | |||||||
| chr9:34103095 | CA | C | 42 | a0001c0001t0001g0035 a0001c0001t0002g0166 a0001c0001t0002g0291 others(39): Show |
43 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.601+3338delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103095 | |||||||
| chr9:34103095 | CAA | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0002g0281 others(5): Show |
8 | HG01109.hp2 HG02615.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+3337_601+3338d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103095 | |||||||
| chr9:34103095 | CAAAA | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(43): Show |
50 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.601+3335_601+3338d others(6): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103095 | |||||||
| chr9:34103095 | CAAAAAA | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0003t0001g0011 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+3333_601+3338d others(8): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103095 | |||||||
| chr9:34103095 | CAAAAAAA | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(70): Show |
78 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.601+3332_601+3338d others(9): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103095 | |||||||
| chr9:34103278 | G | A | 1 | a0001c0001t0014g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.601+3156C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103278 | |||||||
| chr9:34103322 | G | A | 1 | a0002c0002t0002g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.601+3112C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103322 | |||||||
| chr9:34103364 | GCCACTGC others(4): Show |
G | 1 | a0002c0002t0003g0227 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.601+3059_601+3069d others(13): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103364 | |||||||
| chr9:34103405 | C | CA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.601+3028dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103405 | |||||||
| chr9:34103445 | T | A | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.601+2989A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103445 | |||||||
| chr9:34103490 | T | A | 330 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(327): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.601+2944A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103490 | |||||||
| chr9:34103492 | G | A | 1 | a0001c0001t0004g0312 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.601+2942C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103492 | |||||||
| chr9:34103620 | C | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.601+2814G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103620 | |||||||
| chr9:34103703 | T | C | 1 | a0002c0002t0002g0251 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.601+2731A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34103703 | |||||||
| chr9:34104044 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.601+2390T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104044 | |||||||
| chr9:34104135 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.601+2299G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104135 | |||||||
| chr9:34104159 | G | A | 4 | a0001c0001t0004g0299 a0001c0001t0004g0304 a0001c0001t0004g0309 others(1): Show |
4 | HG01074.hp2 HG01255.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+2275C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104159 | |||||||
| chr9:34104166 | G | C | 2 | a0001c0001t0001g0328 a0001c0001t0001g0329 |
2 | NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.601+2268C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104166 | |||||||
| chr9:34104445 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.601+1989A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104445 | |||||||
| chr9:34104518 | A | C | 2 | a0001c0001t0008g0083 a0001c0001t0008g0084 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.601+1916T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104518 | |||||||
| chr9:34104666 | A | C | 1 | a0002c0002t0002g0251 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.601+1768T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104666 | |||||||
| chr9:34104918 | C | CA | 5 | a0001c0001t0003g0248 a0001c0001t0012g0246 a0002c0002t0002g0005 others(2): Show |
7 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+1515dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104918 | |||||||
| chr9:34104990 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.601+1444G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34104990 | |||||||
| chr9:34105018 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.601+1416G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105018 | |||||||
| chr9:34105058 | G | C | 3 | a0002c0002t0002g0005 a0002c0002t0002g0193 a0002c0002t0002g0272 |
5 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+1376C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105058 | |||||||
| chr9:34105113 | C | T | 42 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0002g0293 others(39): Show |
43 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.601+1321G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105113 | |||||||
| chr9:34105132 | A | C | 44 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0002g0291 others(41): Show |
45 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.601+1302T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105132 | |||||||
| chr9:34105252 | C | CA | 6 | a0001c0001t0001g0039 a0001c0001t0001g0134 a0001c0001t0001g0140 others(3): Show |
6 | HG01981.hp1 HG02027.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+1181dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105252 | |||||||
| chr9:34105312 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.601+1122T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105312 | |||||||
| chr9:34105515 | G | A | 5 | a0001c0001t0004g0020 a0001c0001t0004g0314 a0001c0001t0004g0315 others(2): Show |
6 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+919C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105515 | |||||||
| chr9:34105530 | C | T | 3 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0226 |
3 | HG01081.hp2 HG01256.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.601+904G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105530 | |||||||
| chr9:34105564 | T | A | 3 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0226 |
3 | HG01081.hp2 HG01256.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.601+870A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105564 | |||||||
| chr9:34105735 | A | G | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.601+699T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105735 | |||||||
| chr9:34105743 | T | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0043 others(8): Show |
12 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+691A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105743 | |||||||
| chr9:34105755 | C | CT | 89 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.601+678dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105755 | |||||||
| chr9:34105810 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+624C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105810 | |||||||
| chr9:34105822 | C | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.601+612G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105822 | |||||||
| chr9:34105839 | G | C | 1 | a0001c0001t0001g0126 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.601+595C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34105839 | |||||||
| chr9:34106033 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+401G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34106033 | |||||||
| chr9:34106065 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601+369A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34106065 | |||||||
| chr9:34106155 | C | T | 3 | a0001c0001t0002g0157 a0001c0001t0002g0189 a0001c0001t0002g0249 |
3 | HG01884.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601+279G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34106155 | |||||||
| chr9:34106280 | T | C | 1 | a0001c0003t0001g0077 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.601+154A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34106280 | |||||||
| chr9:34106338 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.601+96G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34106338 | |||||||
| chr9:34106412 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.601+22G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 4/8 | chr9 | 34106412 | |||||||
| chr9:34106599 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0147 |
2 | HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.541-105A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/8 | chr9 | 34106599 | |||||||
| chr9:34106775 | C | A | 1 | a0001c0001t0002g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.541-281G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/8 | chr9 | 34106775 | |||||||
| chr9:34106880 | C | T | 1 | a0002c0002t0002g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.541-386G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/8 | chr9 | 34106880 | |||||||
| chr9:34106976 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.540+383A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/8 | chr9 | 34106976 | |||||||
| chr9:34107060 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.540+299A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/8 | chr9 | 34107060 | |||||||
| chr9:34107234 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.540+125A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/8 | chr9 | 34107234 | |||||||
| chr9:34107312 | G | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.540+47C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 3/8 | chr9 | 34107312 | |||||||
| chr9:34108191 | C | T | 1 | a0001c0003t0001g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.334-626G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108191 | |||||||
| chr9:34108310 | T | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(67): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.334-745A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108310 | |||||||
| chr9:34108326 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-761G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108326 | |||||||
| chr9:34108352 | G | C | 4 | a0002c0002t0002g0194 a0002c0002t0002g0228 a0002c0002t0002g0229 others(1): Show |
4 | NA18946.hp1 NA18957.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-787C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108352 | |||||||
| chr9:34108517 | C | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0286 others(2): Show |
5 | HG01109.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-952G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108517 | |||||||
| chr9:34108563 | G | A | 1 | a0001c0001t0004g0327 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.334-998C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108563 | |||||||
| chr9:34108573 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0124 |
2 | HG02293.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.334-1008G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108573 | |||||||
| chr9:34108613 | G | A | 2 | a0001c0001t0004g0245 a0001c0001t0004g0310 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.334-1048C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108613 | |||||||
| chr9:34108623 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-1058G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108623 | |||||||
| chr9:34108678 | C | T | 1 | a0001c0001t0004g0290 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.334-1113G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108678 | |||||||
| chr9:34108793 | C | CA | 13 | a0001c0001t0001g0094 a0001c0001t0001g0110 a0001c0001t0001g0111 others(10): Show |
13 | HG01358.hp1 HG01433.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.334-1229dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108793 | |||||||
| chr9:34108793 | C | CAAAA | 30 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0091 others(27): Show |
35 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.334-1232_334-1229d others(6): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108793 | |||||||
| chr9:34108793 | C | CAAAAA | 7 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(4): Show |
7 | HG00323.hp2 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.334-1233_334-1229d others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108793 | |||||||
| chr9:34108793 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.334-1229_334-1228i others(13): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108793 | |||||||
| chr9:34108801 | A | G | 1 | a0001c0001t0002g0183 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.334-1236T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108801 | |||||||
| chr9:34108801 | AT | A | 9 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0002g0296 others(6): Show |
10 | HG01167.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.334-1237delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108801 | |||||||
| chr9:34108802 | T | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(160): Show |
172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.334-1237A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108802 | |||||||
| chr9:34108804 | A | AAAAAT | 5 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0121 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1240_334-1239i others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108804 | |||||||
| chr9:34108804 | A | T | 2 | a0001c0001t0001g0113 a0001c0001t0015g0120 |
2 | HG01433.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.334-1239T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108804 | |||||||
| chr9:34108806 | T | A | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
120 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.334-1241A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108806 | |||||||
| chr9:34108807 | A | T | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1242T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108807 | |||||||
| chr9:34108808 | A | AAAAT | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0328 others(1): Show |
4 | HG00408.hp2 NA18944.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1244_334-1243i others(6): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108808 | |||||||
| chr9:34108808 | A | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(49): Show |
57 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.334-1243T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108808 | |||||||
| chr9:34108810 | T | A | 20 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0002g0293 others(17): Show |
20 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.334-1245A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108810 | |||||||
| chr9:34108812 | A | AAT | 14 | a0001c0001t0002g0163 a0001c0001t0002g0181 a0001c0001t0002g0243 others(11): Show |
14 | HG00140.hp1 HG00738.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.334-1249_334-1248d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108812 | |||||||
| chr9:34108812 | A | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(72): Show |
81 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.334-1247T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108812 | |||||||
| chr9:34108812 | AAT | A | 4 | a0001c0003t0001g0011 a0001c0003t0001g0077 a0001c0003t0001g0079 others(1): Show |
5 | HG00099.hp1 HG01167.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-1249_334-1248d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108812 | |||||||
| chr9:34108814 | T | A | 1 | a0001c0001t0002g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.334-1249A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108814 | |||||||
| chr9:34108984 | TTA | T | 144 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0074 others(141): Show |
165 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.334-1421_334-1420d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108984 | |||||||
| chr9:34108984 | TTATA | T | 14 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(11): Show |
15 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.334-1423_334-1420d others(6): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108984 | |||||||
| chr9:34108999 | TATATG | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-1439_334-1435d others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34108999 | |||||||
| chr9:34109001 | TA | T | 4 | a0001c0001t0002g0182 a0002c0002t0002g0165 a0002c0002t0002g0200 others(1): Show |
4 | HG00609.hp1 HG01175.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1437delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109001 | |||||||
| chr9:34109001 | TATG | T | 57 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(54): Show |
61 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.334-1439_334-1437d others(5): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109001 | |||||||
| chr9:34109003 | T | G | 4 | a0001c0001t0002g0182 a0002c0002t0002g0165 a0002c0002t0002g0200 others(1): Show |
4 | HG00609.hp1 HG01175.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1438A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109003 | |||||||
| chr9:34109003 | T | TA | 3 | a0001c0001t0001g0035 a0001c0001t0004g0245 a0001c0001t0004g0310 |
3 | HG02622.hp2 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.334-1439_334-1438i others(3): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109003 | |||||||
| chr9:34109004 | G | T | 3 | a0001c0001t0001g0035 a0001c0001t0004g0245 a0001c0001t0004g0310 |
3 | HG02622.hp2 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.334-1439C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109004 | |||||||
| chr9:34109005 | G | T | 4 | a0001c0001t0002g0182 a0002c0002t0002g0165 a0002c0002t0002g0200 others(1): Show |
4 | HG00609.hp1 HG01175.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-1440C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109005 | |||||||
| chr9:34109005 | GT | G | 41 | a0001c0001t0001g0039 a0001c0001t0002g0291 a0001c0001t0002g0292 others(38): Show |
42 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.334-1441delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109005 | |||||||
| chr9:34109005 | GTT | G | 14 | a0001c0001t0001g0054 a0001c0003t0001g0011 a0001c0003t0001g0026 others(11): Show |
15 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.334-1442_334-1441d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109005 | |||||||
| chr9:34109006 | T | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(129): Show |
141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.334-1441A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109006 | |||||||
| chr9:34109054 | G | C | 1 | a0002c0002t0005g0320 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.334-1489C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109054 | |||||||
| chr9:34109524 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.334-1959C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109524 | |||||||
| chr9:34109530 | G | A | 5 | a0001c0001t0004g0020 a0001c0001t0004g0314 a0001c0001t0004g0315 others(2): Show |
6 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-1965C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109530 | |||||||
| chr9:34109574 | G | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(66): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.334-2009C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109574 | |||||||
| chr9:34109667 | T | C | 4 | a0001c0001t0002g0013 a0001c0001t0002g0174 a0001c0001t0002g0175 others(1): Show |
5 | HG02486.hp2 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-2102A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109667 | |||||||
| chr9:34109710 | T | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-2145A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109710 | |||||||
| chr9:34109812 | T | C | 2 | a0002c0002t0002g0231 a0002c0002t0002g0232 |
2 | HG00423.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.334-2247A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109812 | |||||||
| chr9:34109880 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-2315G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109880 | |||||||
| chr9:34109893 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.334-2328C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109893 | |||||||
| chr9:34109908 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0039 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.334-2343C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109908 | |||||||
| chr9:34109911 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.334-2346C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34109911 | |||||||
| chr9:34110040 | TATATATA | T | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-2482_334-2476d others(9): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110040 | |||||||
| chr9:34110042 | TATATA | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-2482_334-2478d others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110042 | |||||||
| chr9:34110139 | A | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-2574T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110139 | |||||||
| chr9:34110194 | T | C | 6 | a0001c0001t0002g0003 a0001c0001t0002g0164 a0001c0001t0002g0166 others(3): Show |
8 | HG02615.hp1 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.334-2629A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110194 | |||||||
| chr9:34110564 | G | A | 1 | a0001c0001t0003g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.334-2999C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110564 | |||||||
| chr9:34110681 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.334-3116G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110681 | |||||||
| chr9:34110783 | C | CAACAA | 43 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0002g0291 others(40): Show |
44 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.334-3223_334-3219d others(7): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110783 | |||||||
| chr9:34110783 | C | CAACAAAA others(3): Show |
47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.334-3228_334-3219d others(12): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110783 | |||||||
| chr9:34110819 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.334-3254G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110819 | |||||||
| chr9:34110848 | C | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-3283G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110848 | |||||||
| chr9:34110985 | G | GT | 75 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0065 others(72): Show |
80 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.334-3421dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110985 | |||||||
| chr9:34110985 | G | GTT | 17 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0128 others(14): Show |
18 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-3422_334-3421d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34110985 | |||||||
| chr9:34111004 | G | A | 83 | a0001c0001t0002g0157 a0001c0001t0002g0189 a0001c0001t0002g0243 others(80): Show |
95 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.334-3439C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111004 | |||||||
| chr9:34111035 | G | A | 17 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0097 others(14): Show |
17 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.334-3470C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111035 | |||||||
| chr9:34111090 | A | G | 1 | a0001c0004t0001g0025 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.334-3525T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111090 | |||||||
| chr9:34111105 | C | T | 91 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.334-3540G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111105 | |||||||
| chr9:34111233 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.334-3668G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111233 | |||||||
| chr9:34111263 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.334-3698A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111263 | |||||||
| chr9:34111372 | G | T | 1 | a0002c0002t0005g0321 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.334-3807C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111372 | |||||||
| chr9:34111378 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.334-3813G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111378 | |||||||
| chr9:34111433 | A | G | 2 | a0002c0002t0002g0208 a0002c0002t0002g0260 |
2 | HG01109.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.334-3868T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111433 | |||||||
| chr9:34111591 | C | A | 1 | a0001c0001t0014g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.334-4026G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111591 | |||||||
| chr9:34111622 | T | C | 13 | a0001c0001t0004g0020 a0001c0001t0004g0284 a0001c0001t0004g0285 others(10): Show |
14 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-4057A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111622 | |||||||
| chr9:34111634 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.334-4069A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111634 | |||||||
| chr9:34111724 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-4159A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111724 | |||||||
| chr9:34111752 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.334-4187C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111752 | |||||||
| chr9:34111940 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.334-4375C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111940 | |||||||
| chr9:34111980 | C | CA | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.334-4416dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111980 | |||||||
| chr9:34111980 | CA | C | 6 | a0001c0001t0002g0004 a0001c0001t0002g0163 a0001c0001t0002g0181 others(3): Show |
8 | HG01175.hp2 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-4416delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34111980 | |||||||
| chr9:34112003 | T | C | 2 | a0001c0001t0002g0172 a0001c0001t0002g0271 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.334-4438A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112003 | |||||||
| chr9:34112011 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.334-4446G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112011 | |||||||
| chr9:34112157 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.334-4592C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112157 | |||||||
| chr9:34112281 | T | C | 1 | a0001c0001t0004g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.334-4716A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112281 | |||||||
| chr9:34112334 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-4769C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112334 | |||||||
| chr9:34112388 | G | A | 1 | a0002c0002t0002g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.334-4823C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112388 | |||||||
| chr9:34112487 | G | T | 2 | a0001c0001t0004g0245 a0001c0001t0004g0310 |
2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.334-4922C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112487 | |||||||
| chr9:34112673 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.334-5108G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112673 | |||||||
| chr9:34112674 | G | A | 4 | a0001c0001t0004g0020 a0001c0001t0004g0314 a0001c0001t0004g0315 others(1): Show |
5 | HG02257.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-5109C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112674 | |||||||
| chr9:34112685 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(67): Show |
75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.334-5120C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112685 | |||||||
| chr9:34112782 | T | C | 1 | a0003c0005t0004g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.334-5217A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112782 | |||||||
| chr9:34112784 | G | A | 1 | a0003c0005t0004g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.334-5219C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112784 | |||||||
| chr9:34112857 | C | T | 1 | a0001c0001t0003g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.334-5292G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112857 | |||||||
| chr9:34112961 | A | C | 4 | a0001c0001t0002g0004 a0001c0001t0002g0182 a0001c0001t0002g0183 others(1): Show |
6 | HG01175.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-5396T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34112961 | |||||||
| chr9:34113019 | T | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-5454A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113019 | |||||||
| chr9:34113176 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-5611G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113176 | |||||||
| chr9:34113214 | G | C | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-5649C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113214 | |||||||
| chr9:34113541 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-5976A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113541 | |||||||
| chr9:34113622 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0039 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.334-6057C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113622 | |||||||
| chr9:34113796 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.334-6231C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113796 | |||||||
| chr9:34113874 | C | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-6309G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113874 | |||||||
| chr9:34113884 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.334-6319C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113884 | |||||||
| chr9:34113964 | C | T | 9 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0002g0293 others(6): Show |
9 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-6399G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113964 | |||||||
| chr9:34113969 | G | A | 28 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(25): Show |
31 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.334-6404C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34113969 | |||||||
| chr9:34114050 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.334-6485C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114050 | |||||||
| chr9:34114108 | C | CA | 96 | a0001c0001t0002g0157 a0001c0001t0002g0189 a0001c0001t0002g0243 others(93): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.334-6544dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114108 | |||||||
| chr9:34114115 | A | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.334-6550T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114115 | |||||||
| chr9:34114163 | G | A | 3 | a0001c0001t0002g0013 a0001c0001t0002g0174 a0001c0001t0002g0175 |
4 | HG02486.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-6598C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114163 | |||||||
| chr9:34114340 | A | G | 4 | a0001c0001t0004g0299 a0001c0001t0004g0304 a0001c0001t0004g0309 others(1): Show |
4 | HG01074.hp2 HG01255.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-6775T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114340 | |||||||
| chr9:34114453 | T | A | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-6888A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114453 | |||||||
| chr9:34114690 | T | C | 4 | a0002c0002t0002g0022 a0002c0002t0002g0234 a0002c0002t0002g0239 others(1): Show |
4 | NA18941.hp2 NA18974.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-7125A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114690 | |||||||
| chr9:34114786 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334-7221A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34114786 | |||||||
| chr9:34115046 | C | T | 1 | a0002c0002t0002g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.334-7481G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115046 | |||||||
| chr9:34115066 | A | G | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-7501T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115066 | |||||||
| chr9:34115078 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.334-7513G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115078 | |||||||
| chr9:34115078 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(176): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-7513G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115078 | |||||||
| chr9:34115099 | G | A | 1 | a0001c0001t0011g0034 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.334-7534C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115099 | |||||||
| chr9:34115189 | A | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0150 |
2 | NA18943.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.334-7624T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115189 | |||||||
| chr9:34115191 | G | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.334-7626C>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115191 | |||||||
| chr9:34115321 | G | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0044 others(5): Show |
8 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.334-7756C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115321 | |||||||
| chr9:34115357 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-7792G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115357 | |||||||
| chr9:34115363 | G | A | 1 | a0001c0001t0004g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.334-7798C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115363 | |||||||
| chr9:34115382 | G | GAGATCGA others(131): Show |
72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-7818_334-7817i others(140): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115382 | |||||||
| chr9:34115402 | T | C | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.334-7837A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115402 | |||||||
| chr9:34115418 | C | T | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.334-7853G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115418 | |||||||
| chr9:34115435 | CA | C | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.334-7871delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115435 | |||||||
| chr9:34115438 | A | G | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.334-7873T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115438 | |||||||
| chr9:34115447 | C | T | 114 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(111): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.334-7882G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115447 | |||||||
| chr9:34115448 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-7883C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115448 | |||||||
| chr9:34115452 | G | GCAGTGGT others(155): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG03139.hp2 NA18974.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.334-7888_334-7887i others(164): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GCAGTGGT others(156): Show |
42 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(39): Show |
47 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.334-7888_334-7887i others(165): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GCAGTGGT others(157): Show |
23 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(20): Show |
23 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.334-7888_334-7887i others(166): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GCAGTGGT others(159): Show |
1 | a0001c0001t0001g0023 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.334-7888_334-7887i others(168): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GCAGTGGT others(160): Show |
1 | a0001c0001t0001g0024 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.334-7888_334-7887i others(169): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GCAGTGGT others(156): Show |
2 | a0001c0001t0001g0095 a0001c0001t0013g0096 |
2 | HG01952.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.334-7888_334-7887i others(165): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GGCTGGGC others(294): Show |
5 | a0001c0001t0001g0044 a0001c0001t0008g0029 a0001c0001t0008g0030 others(2): Show |
5 | HG00621.hp2 HG02630.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-7888_334-7887i others(303): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GGCTGGGC others(295): Show |
76 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.334-7888_334-7887i others(304): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GGCTGGGC others(296): Show |
27 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0063 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.334-7888_334-7887i others(305): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GGCTGGGC others(297): Show |
3 | a0001c0001t0002g0263 a0001c0001t0004g0306 a0001c0003t0009g0087 |
3 | HG01891.hp1 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.334-7888_334-7887i others(306): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GGCTGGGC others(295): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.334-7888_334-7887i others(304): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115452 | G | GGCTGGGC others(295): Show |
1 | a0001c0001t0017g0047 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.334-7888_334-7887i others(304): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115452 | |||||||
| chr9:34115474 | C | T | 1 | a0001c0001t0004g0316 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.334-7909G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115474 | |||||||
| chr9:34115590 | T | G | 2 | a0001c0001t0002g0172 a0001c0001t0002g0271 |
2 | HG02055.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.334-8025A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115590 | |||||||
| chr9:34115597 | CA | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(46): Show |
53 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.334-8033delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115597 | |||||||
| chr9:34115800 | C | T | 3 | a0001c0001t0004g0190 a0001c0001t0004g0191 a0001c0001t0004g0238 |
3 | HG02723.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.334-8235G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34115800 | |||||||
| chr9:34116085 | T | C | 78 | a0001c0001t0002g0325 a0002c0002t0002g0002 a0002c0002t0002g0005 others(75): Show |
90 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.334-8520A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116085 | |||||||
| chr9:34116090 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0061 others(2): Show |
5 | NA18747.hp1 NA19060.hp1 NA19077.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-8525C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116090 | |||||||
| chr9:34116217 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.334-8652G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116217 | |||||||
| chr9:34116228 | T | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-8663A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116228 | |||||||
| chr9:34116305 | G | A | 4 | a0001c0001t0002g0004 a0001c0001t0002g0182 a0001c0001t0002g0183 others(1): Show |
6 | HG01175.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+8718C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116305 | |||||||
| chr9:34116306 | C | T | 41 | a0001c0001t0002g0291 a0001c0001t0002g0292 a0001c0001t0002g0293 others(38): Show |
42 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.333+8717G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116306 | |||||||
| chr9:34116335 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.333+8688C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116335 | |||||||
| chr9:34116342 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.333+8681G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116342 | |||||||
| chr9:34116532 | G | A | 1 | a0001c0001t0002g0261 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.333+8491C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116532 | |||||||
| chr9:34116607 | G | A | 1 | a0003c0005t0004g0301 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.333+8416C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116607 | |||||||
| chr9:34116837 | C | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+8186G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116837 | |||||||
| chr9:34116862 | C | T | 5 | a0001c0001t0004g0020 a0001c0001t0004g0314 a0001c0001t0004g0315 others(2): Show |
6 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.333+8161G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116862 | |||||||
| chr9:34116911 | G | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.333+8112C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116911 | |||||||
| chr9:34116966 | G | A | 4 | a0001c0001t0007g0177 a0001c0001t0007g0178 a0001c0001t0007g0179 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+8057C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116966 | |||||||
| chr9:34116980 | A | C | 1 | a0001c0001t0004g0303 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.333+8043T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34116980 | |||||||
| chr9:34117073 | C | T | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+7950G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117073 | |||||||
| chr9:34117156 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.333+7867G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117156 | |||||||
| chr9:34117256 | A | AT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(77): Show |
87 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.333+7766dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117256 | |||||||
| chr9:34117282 | C | CA | 14 | a0001c0001t0014g0031 a0001c0003t0001g0011 a0001c0003t0001g0026 others(11): Show |
15 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.333+7740dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117282 | |||||||
| chr9:34117401 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.333+7622G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117401 | |||||||
| chr9:34117439 | C | T | 1 | a0001c0001t0004g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.333+7584G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117439 | |||||||
| chr9:34117446 | G | A | 4 | a0001c0001t0002g0164 a0001c0001t0002g0170 a0001c0001t0002g0171 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+7577C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117446 | |||||||
| chr9:34117561 | T | C | 1 | a0001c0001t0003g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.333+7462A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117561 | |||||||
| chr9:34117598 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.333+7425A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117598 | |||||||
| chr9:34117696 | C | T | 1 | a0001c0001t0004g0314 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.333+7327G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117696 | |||||||
| chr9:34117712 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.333+7311G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117712 | |||||||
| chr9:34117780 | G | A | 1 | a0002c0002t0002g0165 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.333+7243C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117780 | |||||||
| chr9:34117863 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333+7160C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34117863 | |||||||
| chr9:34118117 | GATTT | G | 30 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0019 others(27): Show |
34 | HG00438.hp1 HG00673.hp1 HG01993.hp1 others(31): Show |
intron_variant | MODIFIER | c.333+6902_333+6905d others(6): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118117 | |||||||
| chr9:34118147 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+6876C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118147 | |||||||
| chr9:34118295 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.333+6728C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118295 | |||||||
| chr9:34118322 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.333+6701G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118322 | |||||||
| chr9:34118389 | C | T | 1 | a0002c0002t0002g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.333+6634G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118389 | |||||||
| chr9:34118429 | C | T | 3 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0242 |
3 | NA18957.hp1 NA18971.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.333+6594G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118429 | |||||||
| chr9:34118474 | C | T | 1 | a0001c0001t0003g0158 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.333+6549G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118474 | |||||||
| chr9:34118626 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0039 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.333+6397C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118626 | |||||||
| chr9:34118820 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0004g0287 others(5): Show |
8 | HG01123.hp1 HG01255.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+6203G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118820 | |||||||
| chr9:34118901 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.333+6122T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118901 | |||||||
| chr9:34118988 | T | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+6035A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34118988 | |||||||
| chr9:34119014 | T | G | 2 | a0001c0001t0004g0284 a0001c0001t0004g0285 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.333+6009A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119014 | |||||||
| chr9:34119037 | A | C | 2 | a0002c0002t0002g0195 a0002c0002t0002g0196 |
2 | HG01256.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.333+5986T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119037 | |||||||
| chr9:34119071 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.333+5952G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119071 | |||||||
| chr9:34119182 | A | G | 3 | a0001c0001t0007g0177 a0001c0001t0007g0178 a0001c0001t0007g0180 |
3 | HG01069.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.333+5841T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119182 | |||||||
| chr9:34119305 | G | C | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+5718C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119305 | |||||||
| chr9:34119555 | T | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+5468A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119555 | |||||||
| chr9:34119678 | C | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+5345G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119678 | |||||||
| chr9:34119702 | G | GT | 54 | a0001c0001t0002g0164 a0001c0001t0002g0174 a0001c0001t0002g0281 others(51): Show |
56 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.333+5320dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119702 | |||||||
| chr9:34119702 | GT | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(115): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.333+5320delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119702 | |||||||
| chr9:34119763 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.333+5260C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119763 | |||||||
| chr9:34119870 | T | G | 1 | a0001c0001t0002g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+5153A>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119870 | |||||||
| chr9:34119887 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333+5136T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34119887 | |||||||
| chr9:34120044 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+4979T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120044 | |||||||
| chr9:34120059 | C | T | 1 | a0001c0001t0003g0236 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.333+4964G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120059 | |||||||
| chr9:34120135 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.333+4888C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120135 | |||||||
| chr9:34120203 | C | CA | 13 | a0001c0001t0002g0157 a0001c0001t0002g0173 a0001c0001t0002g0313 others(10): Show |
13 | HG00735.hp1 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.333+4819dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120203 | |||||||
| chr9:34120203 | CA | C | 107 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0062 others(104): Show |
118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.333+4819delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120203 | |||||||
| chr9:34120203 | CAA | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
51 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.333+4818_333+4819d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120203 | |||||||
| chr9:34120203 | CAAA | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(75): Show |
84 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.333+4817_333+4819d others(5): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120203 | |||||||
| chr9:34120441 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.333+4582G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120441 | |||||||
| chr9:34120464 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.333+4559G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120464 | |||||||
| chr9:34120507 | C | T | 3 | a0001c0001t0003g0186 a0001c0001t0003g0187 a0001c0001t0003g0188 |
3 | HG01496.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.333+4516G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120507 | |||||||
| chr9:34120539 | C | T | 1 | a0002c0002t0002g0185 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.333+4484G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120539 | |||||||
| chr9:34120564 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.333+4459C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120564 | |||||||
| chr9:34120669 | C | CA | 86 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
91 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.333+4353dupT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120669 | |||||||
| chr9:34120669 | C | CAA | 7 | a0001c0001t0004g0020 a0001c0001t0004g0314 a0001c0001t0004g0315 others(4): Show |
8 | HG01255.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.333+4352_333+4353d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120669 | |||||||
| chr9:34120669 | CA | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(77): Show |
87 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.333+4353delT | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120669 | |||||||
| chr9:34120688 | G | A | 12 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(9): Show |
13 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.333+4335C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120688 | |||||||
| chr9:34120690 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+4333T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120690 | |||||||
| chr9:34120722 | T | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+4301A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120722 | |||||||
| chr9:34120807 | G | A | 1 | a0002c0002t0005g0320 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.333+4216C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120807 | |||||||
| chr9:34120941 | G | C | 1 | a0001c0001t0001g0032 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.333+4082C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34120941 | |||||||
| chr9:34121031 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02055.hp1 HG02602.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+3992C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121031 | |||||||
| chr9:34121422 | C | T | 1 | a0001c0001t0014g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.333+3601G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121422 | |||||||
| chr9:34121512 | G | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+3511C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121512 | |||||||
| chr9:34121566 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.333+3457A>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121566 | |||||||
| chr9:34121568 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.333+3455T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121568 | |||||||
| chr9:34121601 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.333+3422G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121601 | |||||||
| chr9:34121620 | C | A | 1 | a0001c0001t0002g0176 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+3403G>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121620 | |||||||
| chr9:34121637 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.333+3386G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121637 | |||||||
| chr9:34121673 | G | A | 1 | a0002c0002t0005g0321 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.333+3350C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121673 | |||||||
| chr9:34121725 | A | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.333+3298T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121725 | |||||||
| chr9:34121727 | G | A | 1 | a0002c0002t0002g0322 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.333+3296C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121727 | |||||||
| chr9:34121774 | C | T | 2 | a0001c0001t0011g0033 a0001c0001t0011g0034 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.333+3249G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121774 | |||||||
| chr9:34121848 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(82): Show |
91 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.333+3175G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34121848 | |||||||
| chr9:34122115 | C | T | 4 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(1): Show |
4 | HG02630.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+2908G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122115 | |||||||
| chr9:34122376 | G | A | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+2647C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122376 | |||||||
| chr9:34122473 | A | AT | 26 | a0001c0001t0001g0032 a0001c0001t0001g0145 a0001c0001t0001g0146 others(23): Show |
30 | HG00099.hp1 HG00438.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.333+2549dupA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122473 | |||||||
| chr9:34122473 | A | ATT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(58): Show |
66 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.333+2548_333+2549d others(4): Show |
DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122473 | |||||||
| chr9:34122473 | AT | A | 11 | a0001c0001t0002g0325 a0001c0001t0003g0335 a0001c0001t0004g0327 others(8): Show |
12 | HG01255.hp1 HG01993.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.333+2549delA | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122473 | |||||||
| chr9:34122569 | C | T | 5 | a0001c0001t0003g0158 a0001c0001t0003g0159 a0001c0001t0003g0160 others(2): Show |
5 | HG00438.hp1 NA18947.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.333+2454G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122569 | |||||||
| chr9:34122817 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.333+2206C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122817 | |||||||
| chr9:34122864 | C | G | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+2159G>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122864 | |||||||
| chr9:34122888 | C | T | 17 | a0001c0001t0008g0029 a0001c0001t0008g0030 a0001c0001t0008g0083 others(14): Show |
18 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.333+2135G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34122888 | |||||||
| chr9:34123192 | A | T | 1 | a0001c0001t0002g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.333+1831T>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34123192 | |||||||
| chr9:34123437 | A | C | 13 | a0001c0003t0001g0011 a0001c0003t0001g0026 a0001c0003t0001g0027 others(10): Show |
14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.333+1586T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34123437 | |||||||
| chr9:34123731 | T | C | 1 | a0002c0002t0002g0151 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.333+1292A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34123731 | |||||||
| chr9:34123759 | C | T | 1 | a0001c0001t0003g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.333+1264G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34123759 | |||||||
| chr9:34123794 | G | A | 3 | a0001c0003t0009g0085 a0001c0003t0009g0086 a0001c0003t0009g0087 |
3 | HG00140.hp1 HG01515.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.333+1229C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34123794 | |||||||
| chr9:34124137 | G | C | 9 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0003g0330 others(6): Show |
9 | HG01993.hp1 HG02148.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+886C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34124137 | |||||||
| chr9:34124314 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(83): Show |
92 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.333+709C>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34124314 | |||||||
| chr9:34124376 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0089 others(66): Show |
74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.333+647A>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34124376 | |||||||
| chr9:34124479 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01928.hp2 HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.333+544C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34124479 | |||||||
| chr9:34124662 | A | G | 1 | a0001c0001t0004g0155 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.333+361T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34124662 | |||||||
| chr9:34124677 | C | T | 3 | a0001c0003t0001g0026 a0001c0003t0001g0027 a0001c0003t0001g0028 |
3 | HG02735.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.333+346G>A | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34124677 | |||||||
| chr9:34124862 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.333+161T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 2/8 | chr9 | 34124862 | |||||||
| chr9:34125504 | A | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0024 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.79-227T>G | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/8 | chr9 | 34125504 | |||||||
| chr9:34126001 | G | A | 1 | a0001c0001t0001g0336 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.78+353C>T | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/8 | chr9 | 34126001 | |||||||
| chr9:34126233 | A | G | 1 | a0002c0002t0002g0022 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.78+121T>C | DCAF12 | ENSG00000198876.13 | transcript | ENST00000361264.9 | protein_coding | 1/8 | chr9 | 34126233 |