| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1705807-1706321 | Common:3; Rare:148 | ||||
| chr16:1706582-1706635 | Rare:7 | ||||
| chr16:1770785-1770967 | Common:1; Rare:98 | ||||
| chr16:1772328-1772463 | Common:1; Rare:64 | ||||
| chr16:1772729-1772837 | Common:2; Rare:35; Clinvar (pathogenic):1 | ||||
| chr16:1773060-1773229 | Rare:58; Clinvar (pathogenic):1 | ||||
| chr16:1773435-1773649 | Common:1; Rare:91 | ||||
| chr16:1782821-1783052 | Rare:82 | ||||
| chr16:1826762-1827013 | Common:5; Rare:87 | ||||
| chr16:1827135-1827291 | Common:1; Rare:79 | ||||
| chr16:1943160-1943580 | Common:1; Rare:127 | ||||
| chr16:1943605-1943713 | Rare:26 | ||||
| chr16:1959369-1959750 | Common:7; Rare:160 | ||||
| chr16:1963800-1963877 | Common:1; Rare:30 | ||||
| chr16:1964722-1965179 | Common:18; Rare:210 |