| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69726382-69726727 | Common:4; Rare:104 | ||||
| chr16:69762266-69762381 | Common:1; Rare:28 | ||||
| chr16:70114105-70114438 | Common:4; Rare:111 | ||||
| chr16:70299117-70299277 | Rare:35 | ||||
| chr16:70346759-70346971 | Common:2; Rare:103 | ||||
| chr16:70454358-70454619 | Common:1; Rare:69 | ||||
| chr16:70523524-70523905 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:71289176-71289468 | Common:2; Rare:78 | ||||
| chr16:71358605-71358728 | Common:1; Rare:43 | ||||
| chr16:71564911-71565016 | Common:1; Rare:38 | ||||
| chr16:71565023-71565069 | Rare:19 | ||||
| chr16:71565083-71565204 | Common:1; Rare:23 | ||||
| chr16:71626095-71626393 | Common:1; Rare:98 | ||||
| chr16:71626493-71626549 | Common:1; Rare:19 | ||||
| chr16:71664085-71664281 | Rare:45 |