| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50855150-50855983 | Common:8; Rare:156 | ||||
| chr19:50856720-50857026 | Common:5; Rare:66 | ||||
| chr19:50857543-50857940 | Common:2; Rare:69 | ||||
| chr19:50873094-50873519 | Common:3; Rare:86 | ||||
| chr19:50875146-50875390 | Common:2; Rare:52 | ||||
| chr19:50877105-50877813 | Common:7; Rare:157 | ||||
| chr19:50877815-50878481 | Common:4; Rare:138 | ||||
| chr19:51019846-51020096 | Common:2; Rare:37 | ||||
| chr19:51025602-51025842 | Common:2; Rare:78 | ||||
| chr19:51027495-51027712 | Rare:41 | ||||
| chr19:51366325-51366595 | Common:8; Rare:80; Clinvar (benign):2 | ||||
| chr19:51751857-51752187 | Common:2; Rare:69 | ||||
| chr19:51887887-51888065 | Rare:63 | ||||
| chr19:51927398-51927509 | Common:1; Rare:31 | ||||
| chr19:51986780-51987009 | Common:1; Rare:62 |