Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24146587-24146732 | Rare:52 | ||||
chr14:24195418-24195709 | Common:1; Rare:67 | ||||
chr14:24213121-24213189 | Rare:16 | ||||
chr14:24213449-24213589 | Common:1; Rare:50 | ||||
chr14:24232317-24232477 | Common:6; Rare:39 | ||||
chr14:24232770-24232929 | Common:1; Rare:36 | ||||
chr14:24242602-24242774 | Rare:40; Clinvar:1 | ||||
chr14:24271593-24271830 | Common:1; Rare:59 | ||||
chr14:24299749-24299896 | Common:1; Rare:49 | ||||
chr14:24442765-24442971 | Common:5; Rare:62 | ||||
chr14:30622190-30622329 | Rare:51 | ||||
chr14:31207667-31207946 | Common:2; Rare:98 | ||||
chr14:31420526-31420650 | Common:3; Rare:49 | ||||
chr14:31561089-31561442 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076688-32077018 | Common:3; Rare:103 |