| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2959784-2959958 | Common:2; Rare:47 | ||||
| chr12:3077280-3077439 | Common:5; Rare:72 | ||||
| chr12:3753107-3753216 | Rare:31 | ||||
| chr12:3873088-3873157 | Rare:17 | ||||
| chr12:3873316-3873539 | Common:2; Rare:48 | ||||
| chr12:4320931-4321273 | Common:5; Rare:133 | ||||
| chr12:4538431-4538933 | Common:3; Rare:115 | ||||
| chr12:4649041-4649178 | Common:1; Rare:53; Clinvar (benign):2 | ||||
| chr12:6200042-6200480 | Common:4; Rare:124 | ||||
| chr12:6341982-6342183 | Rare:40; Clinvar (benign):1 | ||||
| chr12:6383976-6384250 | Common:1; Rare:63 | ||||
| chr12:6384252-6384452 | Common:1; Rare:54 | ||||
| chr12:6451780-6452046 | Common:3; Rare:45 | ||||
| chr12:6452050-6452236 | Common:1; Rare:40 | ||||
| chr12:6470655-6470765 | Rare:35 |