| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:63863772-63864171 | Common:8; Rare:130 | ||||
| chr3:63912011-63912105 | Rare:29 | ||||
| chr3:64687587-64687775 | Common:1; Rare:49 | ||||
| chr3:66038410-66038642 | Rare:50 | ||||
| chr3:67654583-67654778 | Common:2; Rare:72 | ||||
| chr3:69013590-69013829 | Common:1; Rare:74 | ||||
| chr3:69052208-69052423 | Common:4; Rare:74 | ||||
| chr3:87227162-87227404 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058946-88059294 | Common:2; Rare:128 | ||||
| chr3:88149856-88150012 | Rare:49 | ||||
| chr3:93979918-93980190 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062910-94063080 | Rare:39 | ||||
| chr3:97764439-97764795 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr3:98732434-98732512 | Rare:14 | ||||
| chr3:99638418-99638612 | Common:1; Rare:44 |