| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2812402-2812752 | Common:1; Rare:92 | ||||
| chr12:2812885-2813057 | Rare:47 | ||||
| chr12:2877031-2877268 | Rare:75 | ||||
| chr12:2890692-2890941 | Common:1; Rare:101 | ||||
| chr12:3077259-3077435 | Common:5; Rare:77 | ||||
| chr12:3491314-3491469 | Rare:28 | ||||
| chr12:3673604-3673841 | Common:4; Rare:54 | ||||
| chr12:3873083-3873206 | Rare:38 | ||||
| chr12:3873287-3873581 | Common:5; Rare:66 | ||||
| chr12:4273489-4273830 | Rare:93 | ||||
| chr12:4275433-4275714 | Common:3; Rare:51 | ||||
| chr12:4320934-4321266 | Common:5; Rare:129 | ||||
| chr12:4538431-4538930 | Common:3; Rare:114 | ||||
| chr12:4648994-4649188 | Common:2; Rare:62; Clinvar (benign):2 | ||||
| chr12:4813876-4814028 | Common:1; Rare:27 |