Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:37197844-37198082 | Common:3; Rare:77 | ||||
chr14:38256045-38256271 | Common:1; Rare:60 | ||||
chr14:39114205-39114346 | Common:2; Rare:52 | ||||
chr14:39267029-39267442 | Common:2; Rare:149 | ||||
chr14:39432420-39432618 | Common:6; Rare:66 | ||||
chr14:44961892-44962255 | Common:3; Rare:105 | ||||
chr14:45253078-45253310 | Rare:61 | ||||
chr14:49586317-49586772 | Common:1; Rare:238; Clinvar (benign):1 | ||||
chr14:49598670-49599023 | Common:2; Rare:136 | ||||
chr14:49620561-49620842 | Common:2; Rare:117; Clinvar:3 | ||||
chr14:49688201-49688298 | Rare:33 | ||||
chr14:49852715-49853129 | Common:3; Rare:114 | ||||
chr14:49892944-49893136 | Rare:80 | ||||
chr14:50312170-50312396 | Common:1; Rare:97 | ||||
chr14:50396877-50397015 | Common:2; Rare:40 |