| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:570990-571313 | Common:2; Rare:61 | ||||
| chr12:632252-632456 | Common:1; Rare:30 | ||||
| chr12:642676-643124 | Common:8; Rare:239 | ||||
| chr12:724415-724815 | Common:1; Rare:116 | ||||
| chr12:751030-751510 | Common:2; Rare:212 | ||||
| chr12:754198-754433 | Common:5; Rare:49; Clinvar (benign):4 | ||||
| chr12:1050129-1050329 | Rare:43 | ||||
| chr12:1575995-1576239 | Rare:47 | ||||
| chr12:1606085-1606272 | Common:1; Rare:42 | ||||
| chr12:1641651-1642704 | Common:16; Rare:446 | ||||
| chr12:1656690-1657290 | Common:6; Rare:138 | ||||
| chr12:1661700-1662281 | Common:7; Rare:304 | ||||
| chr12:1706173-1706966 | Common:6; Rare:205 | ||||
| chr12:1707027-1707663 | Common:12; Rare:175 | ||||
| chr12:1740507-1741367 | Common:5; Rare:208 |