| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142149348-142149692 | Common:3; Rare:100 | ||||
| chr3:142225538-142225653 | Common:1; Rare:34 | ||||
| chr3:142447974-142448163 | Common:1; Rare:73 | ||||
| chr3:142578708-142578980 | Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596249-142596459 | Common:2; Rare:58 | ||||
| chr3:142888961-142889026 | Common:2; Rare:12 | ||||
| chr3:143001400-143001634 | Common:3; Rare:87 | ||||
| chr3:143971694-143971847 | Common:1; Rare:73 | ||||
| chr3:143971975-143972074 | Rare:39 | ||||
| chr3:146160977-146161386 | Common:2; Rare:124; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146544540-146544779 | Common:3; Rare:59 | ||||
| chr3:149086445-149086709 | Rare:80 | ||||
| chr3:149129549-149129711 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149657964-149658191 | Rare:48 | ||||
| chr3:149658500-149658687 | Common:1; Rare:42 |