| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1448736-1449017 | Common:5; Rare:99; Clinvar (benign):4 | ||||
| chr16:1493228-1493604 | Common:4; Rare:110 | ||||
| chr16:1533475-1533731 | Common:2; Rare:50 | ||||
| chr16:1612037-1612354 | Common:1; Rare:104; Clinvar:1 | ||||
| chr16:1706047-1706408 | Common:5; Rare:113 | ||||
| chr16:1771515-1771862 | Common:3; Rare:135 | ||||
| chr16:1772602-1772900 | Common:3; Rare:98; Clinvar (pathogenic):2 | ||||
| chr16:1773110-1773473 | Common:2; Rare:153 | ||||
| chr16:1782509-1783023 | Common:4; Rare:172 | ||||
| chr16:1827161-1827232 | Common:1; Rare:33 | ||||
| chr16:1941930-1942194 | Rare:55 | ||||
| chr16:1943157-1943515 | Common:1; Rare:114 | ||||
| chr16:1964450-1965074 | Common:19; Rare:267 | ||||
| chr16:1971883-1972123 | Common:3; Rare:71 | ||||
| chr16:2009678-2009896 | Common:15; Rare:93 |