| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28823705-28824618 | Common:15; Rare:681 | ||||
| chr16:28845434-28845637 | Common:4; Rare:99 | ||||
| chr16:28846200-28846872 | Common:6; Rare:510; Clinvar:20; Clinvar (benign):18 | ||||
| chr16:28863376-28863627 | Rare:105 | ||||
| chr16:28863662-28864075 | Common:8; Rare:252 | ||||
| chr16:28879864-28880084 | Common:6; Rare:123 | ||||
| chr16:28924577-28925524 | Common:10; Rare:689 | ||||
| chr16:28925640-28925874 | Rare:99 | ||||
| chr16:28936474-28937423 | Rare:486; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:28950510-28951101 | Common:4; Rare:398 | ||||
| chr16:28951280-28951660 | Common:2; Rare:174 | ||||
| chr16:28974543-28974887 | Common:4; Rare:313 | ||||
| chr16:29679031-29679235 | Rare:64 | ||||
| chr16:29679374-29679774 | Common:3; Rare:98 | ||||
| chr16:29694920-29695460 | Common:2; Rare:224 |