Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:23580732-23581056 | Rare:64 | ||||
chr16:24570371-24570750 | Common:2; Rare:74 | ||||
chr16:25031457-25031761 | Common:2; Rare:72 | ||||
chr16:29264577-29264784 | Common:5; Rare:30 | ||||
chr16:29575994-29576046 | Rare:4 | ||||
chr16:29924716-29924946 | Common:1; Rare:47 | ||||
chr16:30353044-30353312 | Rare:107 | ||||
chr16:30378819-30378896 | Common:1; Rare:14 | ||||
chr16:30444505-30444660 | Rare:36 | ||||
chr16:30714747-30714803 | Common:1; Rare:8 | ||||
chr16:30756210-30756378 | Rare:53 | ||||
chr16:30875325-30875534 | Rare:67 | ||||
chr16:31090727-31090866 | Rare:26 | ||||
chr16:31191013-31191351 | Common:1; Rare:110; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr16:33707239-33707301 | Common:1; Rare:29 |