| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47080876-47080965 | Rare:29 | ||||
| chr12:47306822-47307002 | Common:2; Rare:42 | ||||
| chr12:47377402-47377701 | Common:1; Rare:52 | ||||
| chr12:48142626-48142881 | Rare:41 | ||||
| chr12:48178862-48178939 | Common:1; Rare:12 | ||||
| chr12:48198132-48198385 | Common:4; Rare:66 | ||||
| chr12:48212677-48212773 | Common:15; Rare:47 | ||||
| chr12:48284191-48284297 | Common:1; Rare:17 | ||||
| chr12:48296701-48296831 | Rare:31 | ||||
| chr12:48307434-48307566 | Common:1; Rare:33 | ||||
| chr12:48488654-48488945 | Common:1; Rare:55 | ||||
| chr12:48592829-48592972 | Rare:25 | ||||
| chr12:48727297-48727469 | Rare:27 | ||||
| chr12:48904781-48905111 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:48916757-48917106 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 |