| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107318729-107318759 | Rare:5 | ||||
| chr12:107684929-107685491 | Common:6; Rare:91 | ||||
| chr12:107685596-107686048 | Common:2; Rare:152 | ||||
| chr12:107760573-107760644 | Rare:12 | ||||
| chr12:107761055-107761304 | Common:4; Rare:99 | ||||
| chr12:108514962-108515397 | Common:2; Rare:132 | ||||
| chr12:108515499-108515781 | Common:1; Rare:52 | ||||
| chr12:108532640-108532815 | Common:1; Rare:33 | ||||
| chr12:108560335-108560780 | Common:3; Rare:112 | ||||
| chr12:108560865-108560933 | Rare:28 | ||||
| chr12:108561099-108561262 | Rare:61 | ||||
| chr12:108561379-108561592 | Common:3; Rare:41 | ||||
| chr12:108561890-108562131 | Common:5; Rare:39 | ||||
| chr12:108562224-108562686 | Common:14; Rare:153; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108701922-108701985 | Rare:13 |