Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24114916-24115381 | Common:2; Rare:128 | ||||
chr14:24141486-24141818 | Common:2; Rare:80 | ||||
chr14:24144196-24144464 | Common:2; Rare:69 | ||||
chr14:24146553-24146881 | Common:1; Rare:106 | ||||
chr14:24195316-24195744 | Common:2; Rare:103 | ||||
chr14:24232248-24232707 | Common:8; Rare:116 | ||||
chr14:24232847-24232958 | Rare:28 | ||||
chr14:24242280-24242407 | Rare:46; Clinvar (benign):1 | ||||
chr14:24242586-24242770 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24267676-24267915 | Common:2; Rare:81 | ||||
chr14:24271488-24271609 | Common:1; Rare:32 | ||||
chr14:24299582-24299854 | Common:4; Rare:62 | ||||
chr14:24429855-24429974 | Rare:28 | ||||
chr14:24442658-24443043 | Common:5; Rare:121 | ||||
chr14:31207582-31207911 | Common:2; Rare:112 |