Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42335134-42335278 | Common:2; Rare:66 | ||||
chr1:42456004-42456353 | Common:1; Rare:93 | ||||
chr1:42456452-42456583 | Rare:58 | ||||
chr1:42682158-42682448 | Common:2; Rare:71 | ||||
chr1:42682603-42682731 | Common:1; Rare:54 | ||||
chr1:42683269-42683465 | Common:3; Rare:78 | ||||
chr1:42766996-42767321 | Common:5; Rare:112; Clinvar (benign):1 | ||||
chr1:42816931-42817136 | Common:1; Rare:56 | ||||
chr1:42817198-42817260 | Rare:18 | ||||
chr1:42817263-42817578 | Rare:101 | ||||
chr1:42846392-42846646 | Common:1; Rare:71 | ||||
chr1:42958823-42959020 | Common:2; Rare:47; Clinvar:3; Clinvar (benign):3 | ||||
chr1:43367946-43368197 | Rare:63 | ||||
chr1:43389763-43389950 | Common:3; Rare:81 | ||||
chr1:43946561-43946983 | Rare:113 |