Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:33200656-33200952 | Common:3; Rare:89 | ||||
chr6:33208443-33208524 | Rare:22 | ||||
chr6:33271653-33272122 | Common:2; Rare:166 | ||||
chr6:33289186-33289644 | Common:4; Rare:101 | ||||
chr6:33298914-33299105 | Rare:48 | ||||
chr6:33322983-33323318 | Common:4; Rare:93 | ||||
chr6:33418048-33418477 | Common:3; Rare:102 | ||||
chr6:33454430-33454612 | Rare:47 | ||||
chr6:34236752-34236914 | Common:2; Rare:64 | ||||
chr6:34248402-34248589 | Rare:35 | ||||
chr6:34392348-34392670 | Rare:125 | ||||
chr6:34424761-34425219 | Common:3; Rare:118; Clinvar (benign):6 | ||||
chr6:34696715-34696982 | Common:1; Rare:62 | ||||
chr6:34757169-34757550 | Common:2; Rare:86 | ||||
chr6:34887938-34888122 | Common:1; Rare:47 |