| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74296719-74296895 | Rare:72 | ||||
| chr16:74304172-74304330 | Common:2; Rare:35 | ||||
| chr16:75116726-75116866 | Common:2; Rare:34 | ||||
| chr16:75433359-75433812 | Common:4; Rare:146 | ||||
| chr16:75566283-75566431 | Rare:81 | ||||
| chr16:75647614-75647809 | Common:2; Rare:98; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:77190720-77191002 | Common:10; Rare:94 | ||||
| chr16:77191136-77191235 | Common:1; Rare:42 | ||||
| chr16:79600702-79600958 | Common:1; Rare:72 | ||||
| chr16:80540934-80541046 | Common:2; Rare:45 | ||||
| chr16:81006832-81007263 | Common:3; Rare:142 | ||||
| chr16:81314776-81315093 | Common:3; Rare:150; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:84116759-84117061 | Common:4; Rare:121 | ||||
| chr16:84145110-84145267 | Rare:86 | ||||
| chr16:84184995-84185266 | Common:1; Rare:80 |