Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:88467380-88467722 | Common:4; Rare:94 | ||||
chr16:53597-53908 | Common:7; Rare:104 | ||||
chr16:1964823-1964920 | Common:3; Rare:35 | ||||
chr16:2268086-2268174 | Common:1; Rare:38 | ||||
chr16:2777235-2777353 | Common:1; Rare:44 | ||||
chr16:3305406-3305508 | Common:1; Rare:31 | ||||
chr16:4476273-4476459 | Common:3; Rare:68 | ||||
chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr16:18801533-18801830 | Common:4; Rare:89 | ||||
chr16:23641257-23641476 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
chr16:24729607-24729722 | Common:6; Rare:63 | ||||
chr16:27549886-27550152 | Common:2; Rare:94 | ||||
chr16:29995610-29995729 | Rare:54 | ||||
chr16:29996088-29996283 | Common:2; Rare:69 | ||||
chr16:30075905-30076034 | Rare:46 |