| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56989363-56989594 | Common:1; Rare:53; Clinvar:1 | ||||
| chr16:57185956-57186335 | Common:1; Rare:107 | ||||
| chr16:57447354-57447517 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:58129311-58129570 | Common:2; Rare:81 | ||||
| chr16:66552476-66552629 | Rare:67 | ||||
| chr16:66934365-66934524 | Rare:58 | ||||
| chr16:67159866-67159941 | Rare:10 | ||||
| chr16:67183948-67184220 | Common:2; Rare:68 | ||||
| chr16:67247458-67247732 | Rare:81 | ||||
| chr16:67481088-67481384 | Common:1; Rare:109 | ||||
| chr16:67528698-67528883 | Rare:53 | ||||
| chr16:67666719-67666861 | Rare:27 | ||||
| chr16:67719286-67719468 | Common:1; Rare:47 | ||||
| chr16:67806546-67806875 | Rare:65 | ||||
| chr16:68023208-68023302 | Common:1; Rare:25 |