Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73851664-73851983 | Common:4; Rare:102 | ||||
chr14:73886819-73886897 | Common:1; Rare:26 | ||||
chr14:73950143-73950325 | Common:3; Rare:79; Clinvar (benign):1 | ||||
chr14:74019269-74019429 | Common:1; Rare:62 | ||||
chr14:74493570-74493788 | Common:3; Rare:83; Clinvar (benign):4 | ||||
chr14:74713053-74713198 | Rare:81 | ||||
chr14:74881840-74881953 | Rare:51 | ||||
chr14:75002741-75002943 | Common:1; Rare:57; Clinvar:2 | ||||
chr14:75063988-75064179 | Common:1; Rare:48 | ||||
chr14:75127008-75127120 | Rare:34 | ||||
chr14:75660809-75661171 | Common:2; Rare:80 | ||||
chr14:75661203-75661316 | Common:2; Rare:32 | ||||
chr14:76151788-76151984 | Rare:66 | ||||
chr14:77377049-77377415 | Common:2; Rare:107 | ||||
chr14:77457561-77457869 | Common:1; Rare:92 |