| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:28863925-28864032 | Rare:23 | ||||
| chr16:28925105-28925369 | Rare:84 | ||||
| chr16:28974650-28974808 | Common:1; Rare:66 | ||||
| chr16:29805376-29805806 | Common:2; Rare:195 | ||||
| chr16:29806201-29806512 | Common:2; Rare:65 | ||||
| chr16:29807944-29808153 | Rare:126 | ||||
| chr16:29817111-29817270 | Rare:55 | ||||
| chr16:29899516-29899634 | Rare:28 | ||||
| chr16:29926142-29926339 | Common:3; Rare:74 | ||||
| chr16:29961965-29962240 | Common:1; Rare:87 | ||||
| chr16:29973780-29973955 | Common:1; Rare:72 | ||||
| chr16:29995569-29995719 | Common:1; Rare:74 | ||||
| chr16:29996023-29996302 | Common:2; Rare:95 | ||||
| chr16:30052957-30053197 | Common:1; Rare:80 | ||||
| chr16:30064298-30064501 | Common:1; Rare:37; Clinvar (benign):1 |