| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28845311-28845607 | Common:2; Rare:87; Clinvar (pathogenic):1 | ||||
| chr16:28846253-28846697 | Common:2; Rare:149; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863494-28864057 | Common:3; Rare:141 | ||||
| chr16:28925104-28925369 | Common:1; Rare:84 | ||||
| chr16:28974669-28974794 | Rare:57 | ||||
| chr16:29805376-29805768 | Common:2; Rare:181 | ||||
| chr16:29807890-29808186 | Rare:165 | ||||
| chr16:29811078-29811321 | Rare:104 | ||||
| chr16:29815924-29816235 | Common:3; Rare:93 | ||||
| chr16:29816260-29816797 | Common:1; Rare:181 | ||||
| chr16:29859167-29859795 | Rare:151 | ||||
| chr16:29862967-29863579 | Common:1; Rare:163 | ||||
| chr16:29900349-29900794 | Common:1; Rare:94 | ||||
| chr16:29926133-29926339 | Common:3; Rare:78 | ||||
| chr16:29973602-29973947 | Common:5; Rare:116 |