| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:140941600-140941911 | Common:2; Rare:115 | ||||
| chr3:141231652-141231888 | Common:2; Rare:83 | ||||
| chr3:141738131-141738461 | Common:1; Rare:129 | ||||
| chr3:141875914-141876251 | Rare:86 | ||||
| chr3:141876447-141876704 | Common:2; Rare:97 | ||||
| chr3:142578711-142578938 | Rare:78; Clinvar:1 | ||||
| chr3:142723937-142724050 | Rare:30 | ||||
| chr3:143001436-143001631 | Common:3; Rare:72 | ||||
| chr3:143971967-143972074 | Rare:42 | ||||
| chr3:146160958-146161364 | Common:2; Rare:127; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:149129549-149129692 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377537-149377822 | Common:1; Rare:73 | ||||
| chr3:149657943-149658175 | Rare:47 | ||||
| chr3:150407994-150408314 | Common:2; Rare:94 | ||||
| chr3:150603151-150603404 | Common:2; Rare:103 |