| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114281476-114281657 | Common:2; Rare:91 | ||||
| chr14:20343209-20343652 | Common:12; Rare:256 | ||||
| chr14:20454804-20455328 | Common:7; Rare:135 | ||||
| chr14:20461739-20461996 | Common:2; Rare:56 | ||||
| chr14:21384235-21384484 | Rare:85 | ||||
| chr14:21437228-21437429 | Common:4; Rare:86 | ||||
| chr14:21456041-21456208 | Common:2; Rare:42 | ||||
| chr14:21476878-21477253 | Common:1; Rare:115 | ||||
| chr14:21511289-21511553 | Rare:67 | ||||
| chr14:22598201-22598270 | Rare:24 | ||||
| chr14:22766560-22766716 | Common:1; Rare:84 | ||||
| chr14:22815351-22815729 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chr14:22815808-22815958 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr14:22829781-22829919 | Rare:50 | ||||
| chr14:22836308-22836615 | Common:4; Rare:69 |