| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67719278-67719481 | Common:1; Rare:57 | ||||
| chr16:67828475-67828792 | Rare:110 | ||||
| chr16:67842245-67842555 | Common:1; Rare:98 | ||||
| chr16:67846986-67847238 | Common:1; Rare:68 | ||||
| chr16:67935704-67935953 | Common:1; Rare:79 | ||||
| chr16:68022949-68023302 | Common:2; Rare:138 | ||||
| chr16:68245161-68245397 | Common:1; Rare:67 | ||||
| chr16:68310896-68311081 | Common:1; Rare:97 | ||||
| chr16:68539151-68539353 | Common:2; Rare:94 | ||||
| chr16:69132537-69132671 | Rare:55 | ||||
| chr16:69339556-69339807 | Rare:99; Clinvar (benign):1 | ||||
| chr16:69424474-69424690 | Common:1; Rare:62 | ||||
| chr16:69726442-69726826 | Common:3; Rare:100 | ||||
| chr16:69762268-69762381 | Common:1; Rare:28 | ||||
| chr16:70114125-70114376 | Common:3; Rare:91 |