Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24147257-24147491 | Common:2; Rare:61 | ||||
chr14:24195383-24195744 | Common:2; Rare:83 | ||||
chr14:24213115-24213194 | Rare:18 | ||||
chr14:24213431-24213529 | Rare:35 | ||||
chr14:24232251-24232936 | Common:9; Rare:165 | ||||
chr14:24240841-24240915 | Rare:22; Clinvar:1 | ||||
chr14:24242268-24242429 | Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24242515-24242774 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):3 | ||||
chr14:24259939-24260222 | Common:1; Rare:99; Clinvar:3; Clinvar (pathogenic):10 | ||||
chr14:24260644-24260962 | Common:1; Rare:88 | ||||
chr14:24263143-24263273 | Common:2; Rare:35 | ||||
chr14:24267697-24267915 | Common:2; Rare:75 | ||||
chr14:24271453-24271665 | Common:2; Rare:61 | ||||
chr14:24299661-24299879 | Common:4; Rare:61 | ||||
chr14:24313217-24313455 | Rare:42 |