| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1573150-1573780 | Common:4; Rare:173 | ||||
| chr16:1580640-1581344 | Common:6; Rare:225; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:1613435-1613741 | Rare:89 | ||||
| chr16:1645760-1646370 | Common:9; Rare:251 | ||||
| chr16:1688136-1689686 | Common:16; Rare:589 | ||||
| chr16:1900060-1900710 | Common:19; Rare:222 | ||||
| chr16:1913310-1913760 | Common:2; Rare:199 | ||||
| chr16:1920863-1921277 | Common:3; Rare:229 | ||||
| chr16:1929649-1929990 | Common:10; Rare:193 | ||||
| chr16:1965522-1965832 | Common:4; Rare:70 | ||||
| chr16:1985385-1985878 | Common:14; Rare:296; Clinvar (benign):2 | ||||
| chr16:1988466-1988645 | Common:7; Rare:28 | ||||
| chr16:2007890-2008518 | Common:9; Rare:279 | ||||
| chr16:2008973-2009153 | Rare:69 | ||||
| chr16:2015416-2015833 | Common:5; Rare:271 |