| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6927559-6927830 | Rare:72 | ||||
| chr12:6937475-6937739 | Common:1; Rare:75 | ||||
| chr12:6943531-6943834 | Common:4; Rare:135 | ||||
| chr12:6943873-6944172 | Common:11; Rare:308; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6946277-6946657 | Common:1; Rare:100 | ||||
| chr12:6970434-6970972 | Common:4; Rare:168; Clinvar (benign):1 | ||||
| chr12:7018412-7018630 | Common:1; Rare:61 | ||||
| chr12:7018830-7019017 | Rare:44 | ||||
| chr12:7091872-7091987 | Rare:28 | ||||
| chr12:7108438-7108695 | Common:1; Rare:75 | ||||
| chr12:7108923-7109015 | Common:12; Rare:27 | ||||
| chr12:7109115-7109329 | Rare:66 | ||||
| chr12:7128858-7129122 | Common:2; Rare:34 | ||||
| chr12:7129993-7130423 | Common:6; Rare:95 | ||||
| chr12:7155631-7156008 | Common:3; Rare:55 |