| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:140941657-140941902 | Common:2; Rare:94 | ||||
| chr3:141231641-141231888 | Common:2; Rare:87 | ||||
| chr3:141402249-141402378 | Common:2; Rare:37 | ||||
| chr3:141486857-141487082 | Common:1; Rare:73 | ||||
| chr3:141738070-141738344 | Common:2; Rare:119 | ||||
| chr3:141876491-141876652 | Common:1; Rare:60 | ||||
| chr3:142149351-142149652 | Common:2; Rare:85 | ||||
| chr3:142225491-142225685 | Common:3; Rare:66 | ||||
| chr3:142447979-142448173 | Common:1; Rare:72 | ||||
| chr3:142596282-142596429 | Common:1; Rare:38 | ||||
| chr3:143001405-143001634 | Common:3; Rare:85 | ||||
| chr3:143971694-143971839 | Common:1; Rare:70 | ||||
| chr3:148991369-148991592 | Common:5; Rare:98 | ||||
| chr3:149086467-149086733 | Rare:78 | ||||
| chr3:149129545-149129718 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 |