| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68084548-68084782 | Rare:42 | ||||
| chr16:68245151-68245413 | Common:1; Rare:78 | ||||
| chr16:68264453-68264572 | Rare:43 | ||||
| chr16:68310922-68311062 | Common:1; Rare:67 | ||||
| chr16:68539169-68539389 | Common:2; Rare:99 | ||||
| chr16:69132528-69132671 | Rare:56 | ||||
| chr16:69339532-69339821 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:69424466-69424678 | Rare:59 | ||||
| chr16:69726446-69726509 | Rare:21 | ||||
| chr16:69726541-69726567 | Rare:8 | ||||
| chr16:69762266-69762381 | Common:1; Rare:28 | ||||
| chr16:70114118-70114376 | Common:3; Rare:93 | ||||
| chr16:70299093-70299292 | Common:1; Rare:45 | ||||
| chr16:70346751-70346971 | Common:2; Rare:109 | ||||
| chr16:70523527-70523861 | Common:3; Rare:110; Clinvar:1; Clinvar (pathogenic):1 |