| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141231678-141231888 | Common:1; Rare:72 | ||||
| chr3:141402075-141402425 | Common:2; Rare:88 | ||||
| chr3:141486857-141487086 | Common:1; Rare:74 | ||||
| chr3:141738137-141738360 | Common:1; Rare:93 | ||||
| chr3:141875989-141876185 | Rare:52 | ||||
| chr3:142225533-142225637 | Common:1; Rare:33 | ||||
| chr3:142447964-142448130 | Common:1; Rare:58 | ||||
| chr3:142578691-142578925 | Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596212-142596443 | Common:3; Rare:61 | ||||
| chr3:142723884-142724050 | Rare:47 | ||||
| chr3:142888839-142889272 | Common:4; Rare:100 | ||||
| chr3:142963599-142963692 | Rare:31 | ||||
| chr3:143001472-143001642 | Common:2; Rare:61 | ||||
| chr3:143119660-143119850 | Rare:56 | ||||
| chr3:143971717-143971825 | Common:1; Rare:47 |