| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31589869-31589963 | Rare:21 | ||||
| chr12:31590096-31590384 | Common:3; Rare:69 | ||||
| chr12:31659131-31659247 | Common:1; Rare:37 | ||||
| chr12:31728993-31729331 | Common:1; Rare:108 | ||||
| chr12:31792221-31792272 | Rare:12 | ||||
| chr12:31959252-31959490 | Common:2; Rare:78 | ||||
| chr12:32106633-32106817 | Common:4; Rare:52 | ||||
| chr12:32399216-32399611 | Common:5; Rare:107 | ||||
| chr12:32399790-32399916 | Common:1; Rare:43 | ||||
| chr12:32501980-32502277 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32679118-32679434 | Common:1; Rare:122; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755467-32755519 | Rare:16; Clinvar (pathogenic):1 | ||||
| chr12:32755860-32755959 | Rare:47 | ||||
| chr12:32896764-32897084 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905575-38905648 | Common:3; Rare:23 |