| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89918721-89918904 | Common:5; Rare:57; Clinvar:2; Clinvar (benign):6 | ||||
| chr16:89921830-89921995 | Rare:38 | ||||
| chr16:89922027-89922182 | Rare:37 | ||||
| chr16:89922659-89922829 | Rare:45 | ||||
| chr16:89922939-89923495 | Common:2; Rare:196 | ||||
| chr16:89948086-89948138 | Rare:14 | ||||
| chr16:89948633-89948831 | Common:2; Rare:54 | ||||
| chr16:89972227-89972309 | Common:1; Rare:19 | ||||
| chr16:89972455-89972897 | Common:3; Rare:165 | ||||
| chr16:90019725-90019815 | Rare:40 | ||||
| chr16:90019836-90019972 | Rare:40 | ||||
| chr16:90022453-90022761 | Common:2; Rare:107; Clinvar:1 | ||||
| chr17:386114-386125 | Common:1; Rare:1 | ||||
| chr17:386182-386291 | Common:3; Rare:23 | ||||
| chr17:409900-410439 | Common:10; Rare:230 |