| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75556197-75556456 | Common:2; Rare:94; Clinvar (benign):5 | ||||
| chr16:75566206-75566422 | Common:2; Rare:106 | ||||
| chr16:75622685-75623085 | Common:5; Rare:107 | ||||
| chr16:75623219-75623466 | Common:3; Rare:88 | ||||
| chr16:75647595-75647864 | Common:4; Rare:134; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648617-75648747 | Rare:52 | ||||
| chr16:77190636-77191031 | Common:13; Rare:133 | ||||
| chr16:77212188-77212334 | Common:4; Rare:65 | ||||
| chr16:77435025-77435330 | Common:6; Rare:135 | ||||
| chr16:77722272-77722611 | Common:4; Rare:118 | ||||
| chr16:77722650-77723000 | Common:2; Rare:106 | ||||
| chr16:77788585-77789152 | Common:3; Rare:318 | ||||
| chr16:78099120-78099730 | Common:4; Rare:227 | ||||
| chr16:79600702-79600906 | Common:1; Rare:57 | ||||
| chr16:80540849-80541028 | Common:3; Rare:69 |