| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:632450-632638 | Common:1; Rare:32 | ||||
| chr12:642738-642867 | Common:2; Rare:37 | ||||
| chr12:642870-643120 | Common:1; Rare:74 | ||||
| chr12:724355-724692 | Rare:69 | ||||
| chr12:751206-751426 | Common:1; Rare:61 | ||||
| chr12:754271-754417 | Common:4; Rare:27; Clinvar (benign):2 | ||||
| chr12:1474815-1474938 | Common:1; Rare:27 | ||||
| chr12:1605348-1605454 | Rare:27 | ||||
| chr12:1606089-1606206 | Rare:22 | ||||
| chr12:1634620-1634930 | Common:2; Rare:69 | ||||
| chr12:1661842-1662035 | Common:1; Rare:93 | ||||
| chr12:1662055-1662180 | Common:1; Rare:28 | ||||
| chr12:1663094-1663295 | Rare:37 | ||||
| chr12:1804636-1804772 | Common:1; Rare:37 | ||||
| chr12:2035022-2035205 | Common:3; Rare:60 |