| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67278058-67278224 | Rare:22 | ||||
| chr16:67278705-67279082 | Rare:68 | ||||
| chr16:67279158-67279628 | Common:1; Rare:127 | ||||
| chr16:67396241-67396616 | Common:1; Rare:98 | ||||
| chr16:67416232-67416547 | Common:3; Rare:73 | ||||
| chr16:67430528-67430691 | Rare:28 | ||||
| chr16:67430882-67431131 | Common:3; Rare:44 | ||||
| chr16:67431275-67431361 | Rare:18; Clinvar (pathogenic):1 | ||||
| chr16:67480509-67480723 | Rare:35 | ||||
| chr16:67480855-67481467 | Common:3; Rare:188 | ||||
| chr16:67528743-67528957 | Rare:45 | ||||
| chr16:67529097-67529332 | Rare:40 | ||||
| chr16:67529378-67529589 | Common:1; Rare:41 | ||||
| chr16:67529675-67529854 | Rare:32 | ||||
| chr16:67530122-67530324 | Common:1; Rare:49 |