Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:22929332-22929630 | Common:1; Rare:79 | ||||
chr14:22982612-22982916 | Common:2; Rare:100 | ||||
chr14:23095093-23095607 | Common:3; Rare:226 | ||||
chr14:23154371-23154508 | Common:3; Rare:38 | ||||
chr14:23286087-23286258 | Rare:42 | ||||
chr14:23567756-23567913 | Rare:32 | ||||
chr14:23953665-23953793 | Common:5; Rare:43 | ||||
chr14:24114916-24115292 | Common:2; Rare:106 | ||||
chr14:24146582-24146741 | Rare:53 | ||||
chr14:24195420-24195744 | Common:1; Rare:74 | ||||
chr14:24232295-24232477 | Common:6; Rare:52 | ||||
chr14:24232636-24232972 | Common:1; Rare:75 | ||||
chr14:24242264-24242397 | Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24242529-24242770 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
chr14:24271466-24271729 | Common:2; Rare:80 |