| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67998968-67999050 | Common:1; Rare:19 | ||||
| chr16:68022949-68023296 | Common:2; Rare:135 | ||||
| chr16:68245161-68245410 | Common:1; Rare:74 | ||||
| chr16:68310922-68311081 | Common:1; Rare:79 | ||||
| chr16:68539151-68539323 | Common:2; Rare:84 | ||||
| chr16:69132547-69132671 | Rare:52 | ||||
| chr16:69339532-69339857 | Common:1; Rare:144; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69726546-69726785 | Common:3; Rare:53 | ||||
| chr16:69762288-69762381 | Rare:22 | ||||
| chr16:70114127-70114376 | Common:3; Rare:89 | ||||
| chr16:70299072-70299288 | Common:1; Rare:47 | ||||
| chr16:70346759-70346996 | Common:2; Rare:114 | ||||
| chr16:70523517-70523861 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71808751-71809009 | Common:1; Rare:111 | ||||
| chr16:71809057-71809306 | Common:3; Rare:85 |