| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:66934350-66934534 | Common:1; Rare:70 | ||||
| chr16:67028989-67029121 | Rare:44 | ||||
| chr16:67109915-67109994 | Rare:25 | ||||
| chr16:67150960-67151065 | Rare:30 | ||||
| chr16:67159885-67160005 | Rare:19 | ||||
| chr16:67170445-67170570 | Common:1; Rare:19 | ||||
| chr16:67183530-67183682 | Rare:38 | ||||
| chr16:67227004-67227167 | Rare:65 | ||||
| chr16:67481070-67481402 | Common:1; Rare:125 | ||||
| chr16:67528700-67528912 | Rare:55 | ||||
| chr16:67545495-67545713 | Rare:71 | ||||
| chr16:67660228-67660379 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:67660749-67661030 | Common:2; Rare:97 | ||||
| chr16:67666711-67666857 | Rare:30 | ||||
| chr16:67828495-67828791 | Rare:101 |