| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42654152-42654604 | Common:3; Rare:206 | ||||
| chr3:42804399-42804671 | Common:4; Rare:157 | ||||
| chr3:43286419-43286654 | Common:4; Rare:190 | ||||
| chr3:43621921-43622365 | Common:4; Rare:250; Clinvar:13; Clinvar (benign):2 | ||||
| chr3:43690750-43690993 | Common:4; Rare:180; Clinvar:12; Clinvar (benign):3 | ||||
| chr3:43691410-43691830 | Common:4; Rare:133 | ||||
| chr3:44338048-44338183 | Common:4; Rare:86 | ||||
| chr3:44338260-44338510 | Common:5; Rare:120 | ||||
| chr3:44338672-44338797 | Common:3; Rare:47 | ||||
| chr3:44477622-44477773 | Common:2; Rare:58 | ||||
| chr3:44510585-44510725 | Common:2; Rare:36 | ||||
| chr3:44624808-44625109 | Common:4; Rare:120 | ||||
| chr3:44648612-44648812 | Rare:50 | ||||
| chr3:44761590-44761862 | Common:6; Rare:180 | ||||
| chr3:44861793-44861918 | Common:2; Rare:57 |