| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67842727-67842812 | Rare:14; Clinvar (pathogenic):1 | ||||
| chr16:67842969-67843135 | Rare:60 | ||||
| chr16:67846378-67847044 | Common:3; Rare:184 | ||||
| chr16:67847075-67847238 | Common:1; Rare:48 | ||||
| chr16:67847551-67847892 | Common:1; Rare:69 | ||||
| chr16:67848026-67848339 | Common:1; Rare:62 | ||||
| chr16:67872872-67873236 | Rare:105 | ||||
| chr16:67873848-67874044 | Rare:29 | ||||
| chr16:67884720-67884900 | Rare:53 | ||||
| chr16:67893015-67893382 | Common:7; Rare:116 | ||||
| chr16:67893484-67893542 | Rare:13 | ||||
| chr16:67893560-67893702 | Rare:33 | ||||
| chr16:67893704-67893769 | Rare:9 | ||||
| chr16:67935621-67936006 | Common:2; Rare:135 | ||||
| chr16:67936258-67936422 | Rare:70 |