| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141402670-141403200 | Common:3; Rare:136 | ||||
| chr3:141486848-141487084 | Common:1; Rare:78 | ||||
| chr3:141487622-141487800 | Rare:39 | ||||
| chr3:141738025-141738393 | Common:2; Rare:156 | ||||
| chr3:141876002-141876233 | Rare:64 | ||||
| chr3:141876445-141876646 | Common:1; Rare:77 | ||||
| chr3:142149433-142149720 | Common:5; Rare:86 | ||||
| chr3:142225402-142225709 | Common:3; Rare:109 | ||||
| chr3:142448007-142448272 | Common:2; Rare:77 | ||||
| chr3:142578691-142579045 | Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596241-142596467 | Common:2; Rare:61 | ||||
| chr3:142723896-142724165 | Common:1; Rare:67 | ||||
| chr3:142724473-142724574 | Common:2; Rare:42 | ||||
| chr3:142963720-142964190 | Common:7; Rare:120 | ||||
| chr3:143001162-143001638 | Common:5; Rare:123 |