| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:140942088-140942251 | Common:2; Rare:35 | ||||
| chr3:141231696-141231888 | Common:1; Rare:66 | ||||
| chr3:141368260-141368572 | Rare:68 | ||||
| chr3:141402235-141402431 | Common:2; Rare:57 | ||||
| chr3:141402684-141402836 | Common:1; Rare:50 | ||||
| chr3:141431980-141432126 | Common:1; Rare:25 | ||||
| chr3:141876470-141876652 | Common:1; Rare:69 | ||||
| chr3:141921829-141922060 | Rare:45 | ||||
| chr3:142447968-142448130 | Common:1; Rare:57 | ||||
| chr3:142578700-142579011 | Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142723948-142724051 | Rare:25 | ||||
| chr3:142888847-142889265 | Common:4; Rare:100 | ||||
| chr3:143001450-143001650 | Common:2; Rare:75 | ||||
| chr3:143971967-143972096 | Common:1; Rare:50 | ||||
| chr3:146160910-146161386 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):2 |