| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24141581-24141862 | Rare:60 | ||||
| chr14:24146564-24146673 | Rare:43 | ||||
| chr14:24171788-24172093 | Common:3; Rare:69 | ||||
| chr14:24195425-24195744 | Common:1; Rare:72 | ||||
| chr14:24232317-24232673 | Common:8; Rare:86 | ||||
| chr14:24242264-24242430 | Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24242562-24242732 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271460-24271604 | Common:1; Rare:41 | ||||
| chr14:24299743-24299862 | Common:2; Rare:34 | ||||
| chr14:24442681-24443019 | Common:5; Rare:108 | ||||
| chr14:26597416-26597621 | Common:1; Rare:38 | ||||
| chr14:28765238-28765397 | Rare:25 | ||||
| chr14:30558847-30559221 | Common:3; Rare:109 | ||||
| chr14:30622013-30622362 | Common:1; Rare:105 | ||||
| chr14:31025351-31025653 | Common:2; Rare:70 |