| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3873318-3873593 | Common:3; Rare:62 | ||||
| chr12:4273734-4273936 | Common:1; Rare:48 | ||||
| chr12:4275748-4275927 | Rare:36 | ||||
| chr12:4320897-4321332 | Common:5; Rare:165 | ||||
| chr12:4321425-4321598 | Rare:33 | ||||
| chr12:4538377-4538959 | Common:3; Rare:149 | ||||
| chr12:4567155-4567318 | Common:1; Rare:35 | ||||
| chr12:4648777-4649216 | Common:2; Rare:117; Clinvar (benign):2 | ||||
| chr12:6200221-6200404 | Common:2; Rare:52 | ||||
| chr12:6341892-6342196 | Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6444182-6444391 | Common:1; Rare:40 | ||||
| chr12:6444831-6445014 | Rare:30 | ||||
| chr12:6451561-6451733 | Rare:40 | ||||
| chr12:6451961-6452267 | Common:3; Rare:65 | ||||
| chr12:6452273-6452331 | Rare:17 |