Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:21363048-21363443 | Common:1; Rare:103 | ||||
chr14:21466083-21466106 | Rare:3 | ||||
chr14:22770904-22771178 | Common:2; Rare:92 | ||||
chr14:23025662-23025916 | Common:3; Rare:44 | ||||
chr14:23561456-23561461 | Rare:1 | ||||
chr14:24006948-24007116 | Common:1; Rare:47 | ||||
chr14:24192429-24192440 | Rare:3 | ||||
chr14:30884375-30884640 | Rare:54; Clinvar (benign):1 | ||||
chr14:30981971-30982027 | Rare:7 | ||||
chr14:31103108-31103253 | Rare:21 | ||||
chr14:31131061-31131242 | Rare:42 | ||||
chr14:32126575-32126594 | Rare:4 | ||||
chr14:32484401-32484487 | Rare:5 | ||||
chr14:34436967-34436987 | Rare:2 | ||||
chr14:34437429-34437706 | Rare:43 |