| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49877836-49878174 | Common:5; Rare:107 | ||||
| chr19:49928563-49928776 | Common:2; Rare:51 | ||||
| chr19:49929107-49929218 | Common:3; Rare:37 | ||||
| chr19:49929270-49929838 | Common:7; Rare:188 | ||||
| chr19:49930023-49930255 | Common:1; Rare:62 | ||||
| chr19:50415583-50415764 | Common:1; Rare:59; Clinvar:4; Clinvar (benign):15 | ||||
| chr19:50476415-50476650 | Rare:99 | ||||
| chr19:50476746-50476862 | Rare:31 | ||||
| chr19:50511016-50511626 | Common:5; Rare:204 | ||||
| chr19:50658157-50658554 | Common:1; Rare:82 | ||||
| chr19:50804571-50804906 | Common:8; Rare:105 | ||||
| chr19:51366271-51366423 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chr19:51367507-51367864 | Common:2; Rare:103 | ||||
| chr19:51927362-51927487 | Common:1; Rare:36 | ||||
| chr19:51986788-51987025 | Common:1; Rare:66 |