| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57752265-57752393 | Rare:33; Clinvar:1 | ||||
| chr12:57772081-57772253 | Rare:61 | ||||
| chr12:57941292-57941671 | Common:5; Rare:109 | ||||
| chr12:59595856-59596098 | Common:5; Rare:55 | ||||
| chr12:62260111-62260420 | Common:1; Rare:116 | ||||
| chr12:62466679-62466829 | Rare:53 | ||||
| chr12:63780080-63780169 | Rare:39; Clinvar (pathogenic):1 | ||||
| chr12:64222239-64222350 | Rare:39 | ||||
| chr12:64404239-64404661 | Common:5; Rare:152 | ||||
| chr12:64452023-64452174 | Common:1; Rare:55 | ||||
| chr12:64759394-64759673 | Common:3; Rare:82; Clinvar:3 | ||||
| chr12:65169414-65169602 | Common:1; Rare:61; Clinvar:1 | ||||
| chr12:66130696-66130878 | Rare:59 | ||||
| chr12:66169952-66170051 | Rare:29 | ||||
| chr12:66302327-66302591 | Common:1; Rare:60 |