| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120725713-120725875 | Common:1; Rare:49; Clinvar:1 | ||||
| chr12:121296662-121296874 | Common:1; Rare:65 | ||||
| chr12:121399889-121400176 | Common:5; Rare:107 | ||||
| chr12:121580241-121580382 | Rare:52 | ||||
| chr12:121672601-121672702 | Common:4; Rare:33 | ||||
| chr12:121712646-121712856 | Common:3; Rare:78 | ||||
| chr12:121802908-121803109 | Common:1; Rare:53 | ||||
| chr12:121803141-121803318 | Rare:50 | ||||
| chr12:121858853-121859023 | Common:1; Rare:29; Clinvar (benign):2 | ||||
| chr12:121888641-121888876 | Common:2; Rare:77 | ||||
| chr12:121918433-121918609 | Common:5; Rare:38 | ||||
| chr12:122266396-122266547 | Common:2; Rare:66 | ||||
| chr12:122399942-122400149 | Rare:43 | ||||
| chr12:122422538-122422791 | Common:3; Rare:81 | ||||
| chr12:122422949-122423056 | Rare:22 |