Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42767010-42767303 | Common:4; Rare:92; Clinvar (benign):1 | ||||
chr1:42817024-42817145 | Common:1; Rare:29 | ||||
chr1:42817236-42817582 | Rare:115 | ||||
chr1:42846412-42846635 | Common:1; Rare:59 | ||||
chr1:42958849-42959042 | Common:1; Rare:50; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43285534-43285690 | Common:2; Rare:28 | ||||
chr1:43358660-43359000 | Common:7; Rare:106 | ||||
chr1:43367961-43368226 | Rare:70 | ||||
chr1:43389747-43389966 | Common:4; Rare:99; Clinvar:1 | ||||
chr1:43530747-43531086 | Common:6; Rare:118 | ||||
chr1:43605410-43605542 | Rare:46 | ||||
chr1:43946585-43947000 | Rare:112 | ||||
chr1:44031433-44031668 | Common:2; Rare:48 | ||||
chr1:44643050-44643155 | Rare:21 | ||||
chr1:44674362-44674755 | Common:3; Rare:115 |