| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:64625317-64625519 | Common:1; Rare:32 | ||||
| chr12:64625745-64625921 | Rare:42 | ||||
| chr12:64669371-64669507 | Common:3; Rare:24 | ||||
| chr12:65156415-65156621 | Common:1; Rare:33 | ||||
| chr12:65170091-65170182 | Rare:26 | ||||
| chr12:65170421-65170577 | Common:1; Rare:70; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:66303605-66303691 | Common:1; Rare:17 | ||||
| chr12:67268531-67268561 | Rare:3 | ||||
| chr12:67698822-67699134 | Rare:48 | ||||
| chr12:68042386-68042624 | Rare:51 | ||||
| chr12:68236594-68236857 | Common:1; Rare:45 | ||||
| chr12:68241120-68241243 | Rare:21 | ||||
| chr12:68365047-68365182 | Rare:33 | ||||
| chr12:68365293-68365624 | Common:1; Rare:57 | ||||
| chr12:68374256-68374515 | Rare:50 |