| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:56041613-56041970 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr12:56104367-56104687 | Common:5; Rare:114 | ||||
| chr12:56106509-56106680 | Common:1; Rare:34 | ||||
| chr12:56116522-56116825 | Common:2; Rare:117 | ||||
| chr12:56118103-56118370 | Common:1; Rare:76 | ||||
| chr12:56152474-56152630 | Rare:48 | ||||
| chr12:56158223-56158403 | Rare:61 | ||||
| chr12:56161483-56161665 | Rare:34 | ||||
| chr12:56181540-56181806 | Rare:66 | ||||
| chr12:56189449-56189673 | Rare:78 | ||||
| chr12:56221827-56222045 | Common:2; Rare:58 | ||||
| chr12:56224263-56224435 | Common:1; Rare:55 | ||||
| chr12:56257511-56257644 | Rare:26 | ||||
| chr12:56258293-56258547 | Common:1; Rare:85 | ||||
| chr12:56267160-56267326 | Common:1; Rare:46 |