| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1680116-1680405 | Common:1; Rare:60 | ||||
| chr16:1706086-1706537 | Common:4; Rare:128; Clinvar (pathogenic):1 | ||||
| chr16:1706613-1706651 | Rare:5 | ||||
| chr16:1764115-1764364 | Rare:86 | ||||
| chr16:1768132-1768533 | Common:4; Rare:159 | ||||
| chr16:1771502-1771705 | Rare:80 | ||||
| chr16:1772603-1772760 | Common:1; Rare:56; Clinvar (pathogenic):1 | ||||
| chr16:1772972-1773197 | Common:2; Rare:79; Clinvar (pathogenic):2 | ||||
| chr16:1782646-1783018 | Common:1; Rare:117 | ||||
| chr16:1816907-1817175 | Common:2; Rare:124 | ||||
| chr16:1826541-1826975 | Common:5; Rare:131 | ||||
| chr16:1827179-1827247 | Rare:39 | ||||
| chr16:1943189-1943497 | Common:1; Rare:92 | ||||
| chr16:1964509-1965198 | Common:21; Rare:299 | ||||
| chr16:1971895-1972103 | Common:1; Rare:58 |