| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66934353-66934524 | Common:1; Rare:65 | ||||
| chr16:67028903-67029105 | Rare:88 | ||||
| chr16:67109802-67109997 | Rare:62 | ||||
| chr16:67159880-67160005 | Rare:21 | ||||
| chr16:67226846-67227201 | Common:1; Rare:132 | ||||
| chr16:67247458-67247738 | Rare:82 | ||||
| chr16:67481079-67481380 | Common:1; Rare:112 | ||||
| chr16:67528661-67528888 | Rare:59 | ||||
| chr16:67660216-67660391 | Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67666748-67666847 | Rare:18 | ||||
| chr16:67719292-67719478 | Common:1; Rare:51 | ||||
| chr16:67806535-67806851 | Rare:62 | ||||
| chr16:67846727-67846977 | Common:1; Rare:68 | ||||
| chr16:67935652-67935953 | Common:1; Rare:98 | ||||
| chr16:67968549-67968863 | Common:2; Rare:107 |