| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2857029-2857196 | Common:1; Rare:40 | ||||
| chr12:2877005-2877268 | Rare:82 | ||||
| chr12:2890510-2890959 | Common:1; Rare:172 | ||||
| chr12:3077246-3077434 | Common:6; Rare:81 | ||||
| chr12:3753092-3753208 | Rare:31 | ||||
| chr12:3873088-3873233 | Rare:42 | ||||
| chr12:3873307-3873535 | Common:4; Rare:48 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4324589-4324712 | Common:1; Rare:48 | ||||
| chr12:4335402-4335543 | Rare:24 | ||||
| chr12:4538413-4538907 | Common:1; Rare:115 | ||||
| chr12:4562080-4562230 | Common:1; Rare:44 | ||||
| chr12:4590038-4590134 | Common:1; Rare:11 | ||||
| chr12:4645140-4645289 | Common:1; Rare:23 | ||||
| chr12:4648964-4649180 | Common:2; Rare:70; Clinvar (benign):2 |