| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:991108-991243 | Common:1; Rare:50 | ||||
| chr12:6452031-6452132 | Common:1; Rare:22 | ||||
| chr12:6493245-6493355 | Common:5; Rare:27 | ||||
| chr12:6970625-6970942 | Common:3; Rare:94 | ||||
| chr12:21501576-21501819 | Common:1; Rare:55 | ||||
| chr12:25195158-25195296 | Common:1; Rare:42 | ||||
| chr12:42326088-42326176 | Rare:24 | ||||
| chr12:43758788-43758991 | Common:2; Rare:61; Clinvar:2 | ||||
| chr12:49018745-49019104 | Common:1; Rare:116; Clinvar (benign):1 | ||||
| chr12:49568117-49568214 | Common:2; Rare:32 | ||||
| chr12:52949840-52949985 | Rare:33 | ||||
| chr12:53097343-53097681 | Common:1; Rare:69 | ||||
| chr12:55725847-55726217 | Rare:80 | ||||
| chr12:55728952-55729107 | Rare:26 | ||||
| chr12:55829528-55829791 | Rare:86 |