| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141368397-141368575 | Rare:38 | ||||
| chr3:141431975-141432207 | Common:2; Rare:33 | ||||
| chr3:143001457-143001634 | Common:2; Rare:62 | ||||
| chr3:146161129-146161186 | Rare:18; Clinvar:1 | ||||
| chr3:150603149-150603321 | Common:1; Rare:63 | ||||
| chr3:152269490-152269682 | Rare:61 | ||||
| chr3:155854374-155854574 | Rare:51 | ||||
| chr3:156548907-156549186 | Common:3; Rare:66 | ||||
| chr3:156674362-156674624 | Common:3; Rare:76 | ||||
| chr3:158732182-158732277 | Common:2; Rare:30 | ||||
| chr3:160399168-160399336 | Rare:46; Clinvar:2 | ||||
| chr3:160399508-160399675 | Rare:38 | ||||
| chr3:160449733-160449857 | Rare:48 | ||||
| chr3:160565432-160565845 | Common:2; Rare:151 | ||||
| chr3:167734819-167735213 | Common:3; Rare:126; Clinvar:1; Clinvar (benign):1 |