| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37594753-37594876 | Rare:34 | ||||
| chr19:37655440-37655549 | Common:2; Rare:42 | ||||
| chr19:37779594-37779660 | Rare:11 | ||||
| chr19:37817208-37817473 | Common:2; Rare:52 | ||||
| chr19:37907051-37907284 | Rare:51 | ||||
| chr19:38224143-38224321 | Rare:47 | ||||
| chr19:38264244-38264676 | Common:6; Rare:106 | ||||
| chr19:38374407-38374812 | Rare:149 | ||||
| chr19:38596099-38596284 | Rare:50 | ||||
| chr19:38647356-38647748 | Common:3; Rare:135 | ||||
| chr19:38724000-38724296 | Rare:99; Clinvar (benign):2 | ||||
| chr19:38831753-38831938 | Common:3; Rare:67; Clinvar (benign):1 | ||||
| chr19:38852329-38852447 | Rare:34 | ||||
| chr19:38899698-38900053 | Rare:104 | ||||
| chr19:38930720-38931019 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):3 |