| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31073716-31073892 | Common:7; Rare:63 | ||||
| chr12:31324080-31324275 | Rare:49 | ||||
| chr12:31325865-31326462 | Common:6; Rare:168 | ||||
| chr12:31659114-31659219 | Common:1; Rare:33 | ||||
| chr12:31728990-31729288 | Common:1; Rare:92 | ||||
| chr12:31959258-31959488 | Common:2; Rare:75 | ||||
| chr12:31959669-31959882 | Common:2; Rare:71 | ||||
| chr12:32106535-32107019 | Common:6; Rare:133 | ||||
| chr12:32107214-32107358 | Common:2; Rare:42 | ||||
| chr12:32107501-32107555 | Rare:14 | ||||
| chr12:32501937-32502286 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32679054-32679465 | Common:2; Rare:146; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755878-32756028 | Common:1; Rare:48 | ||||
| chr12:32896738-32896966 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:33439626-33440012 | Common:3; Rare:120 |