| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12606970-12607071 | Rare:25 | ||||
| chr12:12613472-12614412 | Common:9; Rare:227 | ||||
| chr12:12645427-12645964 | Common:2; Rare:106 | ||||
| chr12:12673110-12673650 | Common:4; Rare:139 | ||||
| chr12:12696920-12697286 | Common:3; Rare:137 | ||||
| chr12:12698139-12698364 | Rare:32 | ||||
| chr12:12714075-12714437 | Rare:83 | ||||
| chr12:12715619-12716332 | Common:5; Rare:225 | ||||
| chr12:12718930-12719882 | Common:4; Rare:333; Clinvar:2 | ||||
| chr12:12720713-12721187 | Common:2; Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:12722699-12723099 | Common:3; Rare:195 | ||||
| chr12:12723818-12724260 | Common:1; Rare:285 | ||||
| chr12:12724888-12725226 | Common:4; Rare:160 | ||||
| chr12:12735110-12735700 | Common:4; Rare:128 | ||||
| chr12:12736731-12736891 | Common:1; Rare:23 |