| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:74407217-74407244 | Rare:2 | ||||
| chr16:79598854-79598931 | Rare:20 | ||||
| chr16:79770327-79770449 | Common:2; Rare:38 | ||||
| chr16:79770527-79770639 | Common:3; Rare:48 | ||||
| chr16:84284274-84284516 | Common:2; Rare:75 | ||||
| chr16:85136926-85137164 | Rare:58 | ||||
| chr16:85183116-85183379 | Common:2; Rare:80 | ||||
| chr16:85286083-85286390 | Rare:64 | ||||
| chr16:85370912-85371182 | Rare:75 | ||||
| chr16:85699689-85699858 | Common:1; Rare:44 | ||||
| chr16:87123720-87123842 | Common:3; Rare:32 | ||||
| chr16:88835466-88835769 | Common:5; Rare:81; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:88925092-88925503 | Common:8; Rare:124 | ||||
| chr16:89291752-89291849 | Rare:16 | ||||
| chr16:90047749-90048051 | Common:8; Rare:29 |