| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141738003-141738353 | Common:3; Rare:140 | ||||
| chr3:141876452-141876682 | Common:1; Rare:87 | ||||
| chr3:142225538-142225701 | Common:1; Rare:50 | ||||
| chr3:142447968-142448130 | Common:1; Rare:57 | ||||
| chr3:142578711-142578963 | Rare:90; Clinvar:1 | ||||
| chr3:142596293-142596451 | Common:1; Rare:43 | ||||
| chr3:143001472-143001631 | Common:2; Rare:57 | ||||
| chr3:143848437-143848518 | Rare:10 | ||||
| chr3:143971689-143971831 | Common:1; Rare:67 | ||||
| chr3:148991223-148991561 | Common:5; Rare:127 | ||||
| chr3:149086475-149086749 | Rare:85 | ||||
| chr3:149129542-149129692 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149752434-149752552 | Common:2; Rare:43 | ||||
| chr3:149813117-149813260 | Common:1; Rare:50 | ||||
| chr3:150603157-150603338 | Common:2; Rare:67 |