| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:64023321-64023529 | Common:2; Rare:93 | ||||
| chr3:69013590-69013785 | Common:1; Rare:57 | ||||
| chr3:69080358-69080468 | Rare:44 | ||||
| chr3:69084811-69085054 | Common:3; Rare:67 | ||||
| chr3:71306014-71306128 | Common:1; Rare:17 | ||||
| chr3:71582029-71582405 | Rare:114 | ||||
| chr3:71583691-71583729 | Rare:11 | ||||
| chr3:71725208-71725520 | Common:2; Rare:112 | ||||
| chr3:71753584-71753704 | Common:3; Rare:57 | ||||
| chr3:75785533-75785688 | Common:3; Rare:13 | ||||
| chr3:87227201-87227334 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:88058917-88059328 | Common:3; Rare:156 | ||||
| chr3:88149818-88149999 | Rare:50 | ||||
| chr3:94062884-94063052 | Rare:46 | ||||
| chr3:97764439-97764569 | Rare:27 |