| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158672545-158672722 | Common:2; Rare:51 | ||||
| chr3:158801984-158802155 | Common:2; Rare:80 | ||||
| chr3:159763936-159764207 | Common:2; Rare:75 | ||||
| chr3:159764353-159764527 | Rare:50 | ||||
| chr3:160399175-160399308 | Rare:35; Clinvar:2 | ||||
| chr3:160399504-160399707 | Rare:57; Clinvar:1 | ||||
| chr3:160449506-160450034 | Common:2; Rare:154 | ||||
| chr3:160565284-160565842 | Common:3; Rare:187 | ||||
| chr3:160755446-160755613 | Common:1; Rare:60 | ||||
| chr3:161221158-161221355 | Common:2; Rare:65 | ||||
| chr3:167734351-167734619 | Rare:75 | ||||
| chr3:167734799-167735240 | Common:4; Rare:145; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735586-167735740 | Rare:37 | ||||
| chr3:168095888-168096230 | Common:1; Rare:114 | ||||
| chr3:169772722-169772832 | Rare:28 |