Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:57447360-57447511 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr16:58001336-58001436 | Rare:29 | ||||
chr16:58129274-58129529 | Common:2; Rare:80 | ||||
chr16:66552520-66552669 | Rare:63 | ||||
chr16:66880352-66880612 | Common:2; Rare:65 | ||||
chr16:66934365-66934524 | Rare:58 | ||||
chr16:67109822-67109988 | Rare:52 | ||||
chr16:67183537-67183771 | Rare:59 | ||||
chr16:67183945-67183989 | Common:1; Rare:15 | ||||
chr16:67226840-67227201 | Common:1; Rare:134 | ||||
chr16:67481079-67481373 | Common:1; Rare:112 | ||||
chr16:67528678-67528883 | Rare:57 | ||||
chr16:67660222-67660414 | Rare:124; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67666728-67666829 | Rare:21 | ||||
chr16:67719306-67719497 | Common:1; Rare:56 |