| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3077233-3077406 | Common:5; Rare:73 | ||||
| chr12:3490637-3490836 | Common:4; Rare:44 | ||||
| chr12:3490980-3491300 | Common:2; Rare:67 | ||||
| chr12:3873057-3873236 | Rare:51 | ||||
| chr12:3873364-3873590 | Common:2; Rare:54 | ||||
| chr12:4273451-4273832 | Rare:99 | ||||
| chr12:4320897-4321293 | Common:5; Rare:152 | ||||
| chr12:4509258-4509658 | Common:6; Rare:141 | ||||
| chr12:4538413-4538933 | Common:3; Rare:124 | ||||
| chr12:4562020-4562320 | Common:2; Rare:90 | ||||
| chr12:4604600-4605150 | Common:7; Rare:154 | ||||
| chr12:4645026-4645426 | Common:3; Rare:121 | ||||
| chr12:4648949-4649435 | Common:2; Rare:129; Clinvar (benign):2 | ||||
| chr12:5432614-5433023 | Common:4; Rare:139 | ||||
| chr12:6341566-6341966 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):6 |