| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1351864-1351992 | Common:1; Rare:69; Clinvar:6; Clinvar (benign):1 | ||||
| chr16:1420710-1420938 | Common:1; Rare:94 | ||||
| chr16:1493263-1493587 | Common:4; Rare:98 | ||||
| chr16:1533434-1533731 | Common:2; Rare:63 | ||||
| chr16:1612037-1612403 | Common:2; Rare:131; Clinvar:1 | ||||
| chr16:1706086-1706383 | Common:3; Rare:92 | ||||
| chr16:1771488-1771854 | Common:3; Rare:148 | ||||
| chr16:1772299-1772821 | Common:4; Rare:227; Clinvar (pathogenic):2 | ||||
| chr16:1773110-1773213 | Rare:31 | ||||
| chr16:1782758-1783009 | Rare:86 | ||||
| chr16:1817231-1817308 | Rare:33 | ||||
| chr16:1826777-1826982 | Common:3; Rare:65 | ||||
| chr16:1827135-1827607 | Common:4; Rare:234 | ||||
| chr16:1943152-1943508 | Common:1; Rare:111 | ||||
| chr16:1964509-1965061 | Common:17; Rare:240 |