| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57772546-57772660 | Common:2; Rare:12 | ||||
| chr12:57941393-57941695 | Common:3; Rare:88 | ||||
| chr12:58920107-58920378 | Common:2; Rare:84 | ||||
| chr12:59595934-59596182 | Common:5; Rare:62 | ||||
| chr12:62260026-62260483 | Common:1; Rare:168 | ||||
| chr12:63150939-63151064 | Rare:27 | ||||
| chr12:63151106-63151166 | Rare:10 | ||||
| chr12:63780065-63780169 | Rare:49; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:64222233-64222349 | Rare:43 | ||||
| chr12:64404226-64404661 | Common:5; Rare:158 | ||||
| chr12:64452036-64452174 | Common:1; Rare:51 | ||||
| chr12:64759115-64759524 | Common:1; Rare:133; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169452-65169602 | Common:1; Rare:49; Clinvar:1 | ||||
| chr12:65278633-65278739 | Rare:29 | ||||
| chr12:66130703-66130861 | Rare:57 |