| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1706047-1706263 | Common:2; Rare:65 | ||||
| chr16:1706614-1706655 | Rare:5 | ||||
| chr16:1771488-1771911 | Common:4; Rare:171 | ||||
| chr16:1773082-1773219 | Rare:47 | ||||
| chr16:1773532-1773632 | Rare:41 | ||||
| chr16:1781732-1781812 | Rare:18 | ||||
| chr16:1782506-1783033 | Common:4; Rare:179 | ||||
| chr16:1826789-1826968 | Common:3; Rare:54 | ||||
| chr16:1827114-1827313 | Common:1; Rare:92 | ||||
| chr16:1827443-1827710 | Common:3; Rare:113 | ||||
| chr16:1943147-1943508 | Common:1; Rare:113 | ||||
| chr16:1959470-1959751 | Common:4; Rare:128 | ||||
| chr16:1964588-1965061 | Common:16; Rare:218 | ||||
| chr16:1971879-1972165 | Common:3; Rare:84 | ||||
| chr16:2047712-2048050 | Rare:168; Clinvar:2; Clinvar (benign):1 |