| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1705981-1706261 | Common:3; Rare:92 | ||||
| chr16:1771368-1772024 | Common:5; Rare:336 | ||||
| chr16:1773072-1773239 | Rare:60; Clinvar (pathogenic):1 | ||||
| chr16:1782524-1783728 | Common:20; Rare:686 | ||||
| chr16:1826785-1826955 | Common:3; Rare:52 | ||||
| chr16:1827161-1827311 | Common:1; Rare:78 | ||||
| chr16:1943154-1943550 | Common:1; Rare:125 | ||||
| chr16:1959400-1959643 | Common:5; Rare:107 | ||||
| chr16:1964776-1965069 | Common:12; Rare:134 | ||||
| chr16:1971879-1972107 | Common:3; Rare:66 | ||||
| chr16:1983979-1984296 | Common:4; Rare:112; Clinvar (benign):4 | ||||
| chr16:2009620-2010060 | Common:17; Rare:168 | ||||
| chr16:2026630-2026900 | Common:3; Rare:86 | ||||
| chr16:2047848-2048028 | Rare:75; Clinvar:2 | ||||
| chr16:2135883-2136188 | Common:1; Rare:144 |