Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:25015329-25015461 | Common:2; Rare:46 | ||||
chr16:25111468-25111898 | Common:2; Rare:131 | ||||
chr16:25257440-25257590 | Rare:54 | ||||
chr16:25257817-25258045 | Common:6; Rare:99 | ||||
chr16:25258192-25258281 | Rare:45 | ||||
chr16:25258288-25258375 | Common:3; Rare:48 | ||||
chr16:27203407-27203540 | Rare:39 | ||||
chr16:27203716-27203995 | Common:3; Rare:86 | ||||
chr16:27268724-27268912 | Common:1; Rare:68 | ||||
chr16:27549861-27550213 | Common:2; Rare:141 | ||||
chr16:28483847-28484021 | Rare:31; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr16:28491763-28492117 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):7 | ||||
chr16:28554138-28554363 | Common:4; Rare:85 | ||||
chr16:28822580-28822761 | Rare:72 | ||||
chr16:28824282-28824570 | Common:2; Rare:96 |