| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67999032-67999050 | Rare:8 | ||||
| chr16:68023209-68023325 | Common:1; Rare:31 | ||||
| chr16:68084687-68084829 | Rare:29 | ||||
| chr16:68234445-68234849 | Rare:64 | ||||
| chr16:68235315-68235620 | Common:1; Rare:70 | ||||
| chr16:68245161-68245410 | Common:1; Rare:74 | ||||
| chr16:68310915-68311081 | Common:1; Rare:83 | ||||
| chr16:68737108-68737462 | Common:4; Rare:124; Clinvar:11; Clinvar (benign):24 | ||||
| chr16:68823130-68823572 | Common:4; Rare:98; Clinvar:23; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr16:69132528-69132671 | Rare:56 | ||||
| chr16:69187019-69187197 | Rare:69 | ||||
| chr16:69339478-69339823 | Common:2; Rare:151; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69351650-69351711 | Common:1; Rare:21 | ||||
| chr16:69424363-69424840 | Common:2; Rare:137 | ||||
| chr16:69566227-69566325 | Common:1; Rare:25 |