| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:50742313-50742426 | Common:2; Rare:43 | ||||
| chr16:50742700-50742767 | Rare:9 | ||||
| chr16:53054720-53055307 | Common:3; Rare:126 | ||||
| chr16:53055456-53055504 | Common:3; Rare:21 | ||||
| chr16:53099070-53099235 | Rare:31 | ||||
| chr16:53099590-53099815 | Rare:46 | ||||
| chr16:53130349-53130593 | Common:4; Rare:59 | ||||
| chr16:53130758-53131061 | Common:2; Rare:103 | ||||
| chr16:53207916-53207974 | Rare:9 | ||||
| chr16:53208270-53208550 | Rare:55 | ||||
| chr16:53434332-53434554 | Common:1; Rare:76 | ||||
| chr16:53434758-53434930 | Common:1; Rare:54 | ||||
| chr16:53435481-53435623 | Common:1; Rare:28 | ||||
| chr16:53503185-53503789 | Common:10; Rare:177 | ||||
| chr16:53703797-53704222 | Common:1; Rare:133; Clinvar:5; Clinvar (benign):2 |