| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8780088-8780337 | Common:2; Rare:54 | ||||
| chr12:9760809-9761027 | Common:2; Rare:31 | ||||
| chr12:9869221-9869544 | Common:1; Rare:44 | ||||
| chr12:9869621-9869915 | Common:4; Rare:56 | ||||
| chr12:10613528-10613686 | Common:1; Rare:64 | ||||
| chr12:10674072-10674354 | Rare:56 | ||||
| chr12:10723321-10723668 | Common:4; Rare:99 | ||||
| chr12:11171597-11171749 | Common:2; Rare:52 | ||||
| chr12:11649708-11650099 | Common:1; Rare:104 | ||||
| chr12:12357001-12357196 | Common:4; Rare:103 | ||||
| chr12:12696625-12696741 | Rare:40 | ||||
| chr12:12717100-12717443 | Rare:116; Clinvar (benign):1 | ||||
| chr12:12725250-12725519 | Common:3; Rare:66 | ||||
| chr12:12725642-12725975 | Common:3; Rare:76 | ||||
| chr12:13000257-13000452 | Common:1; Rare:52 |