| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1414687-1414889 | Common:1; Rare:59 | ||||
| chr16:1420698-1420938 | Common:1; Rare:104 | ||||
| chr16:1459173-1459540 | Common:17; Rare:76; Clinvar:1 | ||||
| chr16:1533474-1533777 | Common:2; Rare:59 | ||||
| chr16:1612019-1612335 | Common:1; Rare:104; Clinvar:1 | ||||
| chr16:1706086-1706375 | Common:2; Rare:90 | ||||
| chr16:1771494-1771841 | Common:3; Rare:138 | ||||
| chr16:1772602-1772786 | Common:1; Rare:66; Clinvar (pathogenic):1 | ||||
| chr16:1772816-1773209 | Common:3; Rare:134; Clinvar (pathogenic):2 | ||||
| chr16:1782503-1783026 | Common:4; Rare:178 | ||||
| chr16:1826757-1826975 | Common:3; Rare:73 | ||||
| chr16:1827157-1827252 | Common:1; Rare:48 | ||||
| chr16:1943152-1943517 | Common:1; Rare:116 | ||||
| chr16:1964450-1964992 | Common:18; Rare:235 | ||||
| chr16:1971913-1972103 | Common:1; Rare:54 |