| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121536994-121537375 | Common:3; Rare:78 | ||||
| chr12:121537794-121537875 | Rare:26 | ||||
| chr12:121579060-121579424 | Common:2; Rare:69 | ||||
| chr12:121579602-121579822 | Common:2; Rare:41 | ||||
| chr12:121580213-121580392 | Rare:55 | ||||
| chr12:121580423-121580668 | Common:1; Rare:36 | ||||
| chr12:121580982-121581194 | Rare:31 | ||||
| chr12:121626246-121626943 | Common:8; Rare:312; Clinvar:7; Clinvar (benign):2 | ||||
| chr12:121627220-121627434 | Common:1; Rare:39 | ||||
| chr12:121669561-121669750 | Common:1; Rare:32 | ||||
| chr12:121672528-121672722 | Common:4; Rare:55 | ||||
| chr12:121712602-121712848 | Common:5; Rare:98 | ||||
| chr12:121792882-121793227 | Common:2; Rare:88 | ||||
| chr12:121793586-121793829 | Common:1; Rare:87 | ||||
| chr12:121793894-121794134 | Common:3; Rare:66 |