| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27268674-27268919 | Common:1; Rare:88 | ||||
| chr16:27313758-27314034 | Common:5; Rare:74 | ||||
| chr16:27314332-27314704 | Common:2; Rare:70 | ||||
| chr16:27401997-27402030 | Common:1; Rare:5 | ||||
| chr16:27402044-27402322 | Common:2; Rare:66 | ||||
| chr16:27402332-27402598 | Common:2; Rare:55 | ||||
| chr16:27427073-27427299 | Common:2; Rare:38 | ||||
| chr16:27549812-27550224 | Common:2; Rare:159 | ||||
| chr16:28211116-28211318 | Common:2; Rare:54 | ||||
| chr16:28211808-28211900 | Rare:31 | ||||
| chr16:28211908-28212365 | Common:5; Rare:146 | ||||
| chr16:28491441-28491589 | Rare:48; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr16:28491865-28492213 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:28492251-28492445 | Common:2; Rare:31; Clinvar (benign):1 | ||||
| chr16:28494031-28494402 | Common:3; Rare:67 |