| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:75555825-75556159 | Common:1; Rare:136; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr16:75556161-75556455 | Common:3; Rare:109; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr16:75565862-75565902 | Common:1; Rare:9 | ||||
| chr16:75566187-75566434 | Common:2; Rare:112 | ||||
| chr16:75622950-75623034 | Common:1; Rare:22 | ||||
| chr16:75623135-75623439 | Common:6; Rare:112 | ||||
| chr16:75647373-75647895 | Common:5; Rare:228; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75647917-75648733 | Rare:307 | ||||
| chr16:77190625-77191092 | Common:14; Rare:157 | ||||
| chr16:77191101-77191261 | Common:2; Rare:64 | ||||
| chr16:77191521-77191571 | Common:2; Rare:25 | ||||
| chr16:77212091-77212181 | Rare:33 | ||||
| chr16:77212257-77212501 | Common:2; Rare:96 | ||||
| chr16:77212521-77213147 | Common:10; Rare:204 | ||||
| chr16:77722259-77722739 | Common:5; Rare:169 |