| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50820820-50821147 | Rare:68 | ||||
| chr19:51108298-51108626 | Common:1; Rare:74 | ||||
| chr19:51108829-51108891 | Rare:15 | ||||
| chr19:51339753-51340069 | Common:1; Rare:70 | ||||
| chr19:51366267-51366649 | Common:8; Rare:118; Clinvar (benign):2 | ||||
| chr19:51367437-51367935 | Common:5; Rare:161 | ||||
| chr19:51367944-51368024 | Rare:29 | ||||
| chr19:51368026-51368175 | Common:1; Rare:55 | ||||
| chr19:51372878-51373149 | Common:2; Rare:45 | ||||
| chr19:51417548-51417684 | Common:2; Rare:42 | ||||
| chr19:51571114-51571298 | Common:4; Rare:51 | ||||
| chr19:51646992-51647077 | Rare:15 | ||||
| chr19:51904929-51905159 | Common:3; Rare:73 | ||||
| chr19:51927293-51927487 | Common:1; Rare:61 | ||||
| chr19:51986771-51987025 | Common:1; Rare:71 |