Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:22929353-22929613 | Rare:60 | ||||
chr14:23095426-23095564 | Common:2; Rare:53 | ||||
chr14:23321653-23321818 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr14:23323696-23324051 | Common:1; Rare:78 | ||||
chr14:23953631-23953841 | Common:8; Rare:85 | ||||
chr14:23988782-23988943 | Common:7; Rare:67 | ||||
chr14:24114478-24114831 | Common:1; Rare:85 | ||||
chr14:24114921-24115287 | Common:2; Rare:104 | ||||
chr14:24144228-24144409 | Common:2; Rare:48 | ||||
chr14:24146537-24146693 | Rare:62 | ||||
chr14:24163735-24163899 | Common:1; Rare:45 | ||||
chr14:24195425-24195753 | Common:1; Rare:75 | ||||
chr14:24232317-24232698 | Common:8; Rare:88 | ||||
chr14:24232820-24232959 | Common:1; Rare:31 | ||||
chr14:24299722-24299877 | Common:4; Rare:46 |