Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20343190-20343669 | Common:12; Rare:288 | ||||
chr14:20413420-20413501 | Common:2; Rare:20 | ||||
chr14:20454772-20455316 | Common:7; Rare:142 | ||||
chr14:20455322-20455564 | Rare:56 | ||||
chr14:20461817-20462016 | Common:2; Rare:46 | ||||
chr14:20684479-20684618 | Common:1; Rare:23; Clinvar (benign):1 | ||||
chr14:20989701-20990029 | Common:7; Rare:77 | ||||
chr14:20999073-20999311 | Rare:48 | ||||
chr14:21042118-21042373 | Common:1; Rare:46 | ||||
chr14:21383911-21384053 | Common:1; Rare:57 | ||||
chr14:21456041-21456134 | Common:2; Rare:23 | ||||
chr14:21476643-21476665 | Rare:10 | ||||
chr14:21476854-21477271 | Common:2; Rare:138 | ||||
chr14:21511262-21511549 | Rare:82 | ||||
chr14:22766554-22766710 | Common:1; Rare:83 |