| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120469430-120470042 | Common:7; Rare:185 | ||||
| chr12:120495864-120496262 | Common:7; Rare:135 | ||||
| chr12:120581358-120581547 | Common:1; Rare:72 | ||||
| chr12:121580241-121580484 | Rare:75 | ||||
| chr12:121802931-121803069 | Rare:36 | ||||
| chr12:122364444-122364741 | Common:1; Rare:44 | ||||
| chr12:122526911-122527262 | Common:3; Rare:109 | ||||
| chr12:122716771-122716811 | Rare:17 | ||||
| chr12:122980602-122980777 | Common:1; Rare:65 | ||||
| chr12:123233109-123233490 | Common:2; Rare:123; Clinvar:1 | ||||
| chr12:123364820-123364978 | Common:3; Rare:61 | ||||
| chr12:123584384-123584744 | Common:4; Rare:132 | ||||
| chr12:123602031-123602156 | Common:3; Rare:44 | ||||
| chr12:123633624-123633840 | Common:1; Rare:99; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972993-123973299 | Common:2; Rare:95 |