Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24195400-24195737 | Common:2; Rare:74 | ||||
chr14:24213044-24213194 | Rare:27 | ||||
chr14:24213408-24213529 | Rare:44 | ||||
chr14:24213558-24213597 | Common:1; Rare:10 | ||||
chr14:24232260-24232954 | Common:9; Rare:167 | ||||
chr14:24236916-24237146 | Common:2; Rare:44 | ||||
chr14:24237171-24237306 | Common:1; Rare:48 | ||||
chr14:24242187-24242433 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
chr14:24242547-24242781 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
chr14:24259920-24260168 | Rare:93; Clinvar:3; Clinvar (pathogenic):11 | ||||
chr14:24263062-24263255 | Rare:42; Clinvar:2 | ||||
chr14:24263500-24263729 | Common:3; Rare:40 | ||||
chr14:24264198-24264508 | Common:3; Rare:47 | ||||
chr14:24267658-24267916 | Common:2; Rare:87 | ||||
chr14:24271411-24271709 | Common:2; Rare:85 |