| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1678616-1678777 | Common:3; Rare:44 | ||||
| chr16:1705807-1706323 | Common:3; Rare:148 | ||||
| chr16:1706590-1706654 | Rare:8 | ||||
| chr16:1770846-1770996 | Common:2; Rare:79 | ||||
| chr16:1771499-1771675 | Rare:70 | ||||
| chr16:1771684-1771868 | Common:3; Rare:69 | ||||
| chr16:1773003-1773277 | Common:2; Rare:110; Clinvar (pathogenic):2 | ||||
| chr16:1773416-1773687 | Common:1; Rare:123 | ||||
| chr16:1782546-1783043 | Common:3; Rare:165 | ||||
| chr16:1826775-1826948 | Common:2; Rare:51 | ||||
| chr16:1827161-1827264 | Common:1; Rare:54 | ||||
| chr16:1943154-1943583 | Common:1; Rare:130 | ||||
| chr16:1943609-1943703 | Rare:22 | ||||
| chr16:1959370-1959668 | Common:6; Rare:122 | ||||
| chr16:1963580-1963869 | Common:10; Rare:113 |