| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1420714-1420918 | Common:1; Rare:82 | ||||
| chr16:1493264-1493587 | Common:4; Rare:98 | ||||
| chr16:1533437-1533694 | Common:2; Rare:54 | ||||
| chr16:1771502-1771841 | Common:3; Rare:133 | ||||
| chr16:1772602-1772898 | Common:3; Rare:98; Clinvar (pathogenic):2 | ||||
| chr16:1782508-1782768 | Common:4; Rare:84 | ||||
| chr16:1816912-1817175 | Common:2; Rare:122 | ||||
| chr16:1826761-1826982 | Common:3; Rare:72 | ||||
| chr16:1827171-1827538 | Common:3; Rare:192 | ||||
| chr16:1943133-1943503 | Common:1; Rare:117 | ||||
| chr16:1964450-1965061 | Common:18; Rare:266 | ||||
| chr16:1971893-1972106 | Common:1; Rare:61 | ||||
| chr16:1974943-1975223 | Common:2; Rare:124 | ||||
| chr16:2035624-2035931 | Common:3; Rare:95 | ||||
| chr16:2047225-2047432 | Rare:53 |