| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51226066-51226505 | Common:6; Rare:353 | ||||
| chr19:51246050-51246520 | Common:3; Rare:84 | ||||
| chr19:51338738-51339761 | Common:1; Rare:376 | ||||
| chr19:51339662-51340243 | Common:6; Rare:509 | ||||
| chr19:51340170-51340280 | Rare:37 | ||||
| chr19:51365532-51365897 | Common:5; Rare:124 | ||||
| chr19:51365855-51366255 | Common:3; Rare:51 | ||||
| chr19:51366246-51366694 | Common:53; Rare:659; Clinvar (benign):14 | ||||
| chr19:51366689-51367124 | Common:7; Rare:215 | ||||
| chr19:51367415-51367927 | Common:12; Rare:610 | ||||
| chr19:51367940-51368508 | Common:5; Rare:408 | ||||
| chr19:51368489-51368960 | Common:7; Rare:205 | ||||
| chr19:51368880-51369867 | Common:14; Rare:268 | ||||
| chr19:51372886-51373286 | Common:2; Rare:72 | ||||
| chr19:51390408-51391364 | Common:42; Rare:705 |