| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4831655-4832044 | Common:4; Rare:83 | ||||
| chr19:5622695-5623185 | Common:5; Rare:196 | ||||
| chr19:5680485-5680758 | Rare:83 | ||||
| chr19:5791150-5791343 | Common:5; Rare:60 | ||||
| chr19:5903629-5903935 | Common:2; Rare:135; Clinvar:6; Clinvar (benign):6 | ||||
| chr19:5978066-5978393 | Common:3; Rare:123 | ||||
| chr19:6393119-6393238 | Common:2; Rare:29 | ||||
| chr19:6478803-6479035 | Common:2; Rare:83 | ||||
| chr19:6481713-6481862 | Common:1; Rare:44 | ||||
| chr19:6590949-6591334 | Common:2; Rare:84 | ||||
| chr19:6767408-6767584 | Rare:25 | ||||
| chr19:7348773-7349225 | Common:2; Rare:95 | ||||
| chr19:7535569-7535764 | Common:3; Rare:71 | ||||
| chr19:7629531-7629873 | Common:5; Rare:121; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636940-7637184 | Common:3; Rare:69; Clinvar (benign):1 |