| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:8720546-8720765 | Common:2; Rare:59 | ||||
| chr16:8797631-8797866 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868978-8869254 | Common:4; Rare:123 | ||||
| chr16:10385992-10386073 | Rare:32 | ||||
| chr16:10743701-10743861 | Rare:66 | ||||
| chr16:10818576-10818729 | Common:2; Rare:49 | ||||
| chr16:10944332-10944632 | Common:1; Rare:92 | ||||
| chr16:11586900-11587031 | Common:1; Rare:42 | ||||
| chr16:11668204-11668517 | Common:3; Rare:135 | ||||
| chr16:11851513-11851641 | Rare:63 | ||||
| chr16:11915900-11916227 | Common:2; Rare:131 | ||||
| chr16:11976615-11976766 | Common:2; Rare:57 | ||||
| chr16:14632729-14632983 | Common:1; Rare:84 | ||||
| chr16:15094247-15094434 | Rare:85 | ||||
| chr16:15395912-15396031 | Rare:43 |