| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139389518-139389869 | Common:2; Rare:113 | ||||
| chr3:139539554-139539697 | Common:3; Rare:51 | ||||
| chr3:139539707-139539751 | Rare:12 | ||||
| chr3:140941650-140941878 | Common:2; Rare:87 | ||||
| chr3:141231675-141231911 | Common:1; Rare:82 | ||||
| chr3:141876480-141876652 | Common:1; Rare:63 | ||||
| chr3:142225486-142225660 | Common:3; Rare:59 | ||||
| chr3:142447979-142448130 | Common:1; Rare:50 | ||||
| chr3:142578721-142578953 | Rare:79; Clinvar:1 | ||||
| chr3:142596287-142596459 | Common:1; Rare:46 | ||||
| chr3:143001248-143001631 | Common:5; Rare:108 | ||||
| chr3:149086445-149086699 | Rare:76 | ||||
| chr3:149129549-149129676 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377621-149377843 | Common:1; Rare:53 | ||||
| chr3:149657953-149658190 | Rare:50 |