Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:30665139-30665394 | Common:1; Rare:73 | ||||
chr16:30756567-30756947 | Rare:139; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr16:30820651-30820772 | Rare:19 | ||||
chr16:30875325-30875594 | Rare:82 | ||||
chr16:30892734-30892966 | Common:1; Rare:75 | ||||
chr16:31063519-31063802 | Rare:62 | ||||
chr16:31071898-31072131 | Common:3; Rare:33 | ||||
chr16:31118482-31118596 | Common:1; Rare:16 | ||||
chr16:31492268-31492485 | Common:1; Rare:55 | ||||
chr16:31553561-31553664 | Common:1; Rare:19 | ||||
chr16:31568708-31568744 | Rare:5 | ||||
chr16:31700383-31700617 | Common:3; Rare:53 | ||||
chr16:32264365-32264502 | Common:1; Rare:39 | ||||
chr16:32600195-32600351 | Common:2; Rare:33 | ||||
chr16:33516684-33516947 | Common:4; Rare:89 |