| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6393379-6393541 | Common:1; Rare:45 | ||||
| chr19:6590983-6591186 | Common:1; Rare:49 | ||||
| chr19:6591223-6591375 | Common:1; Rare:27 | ||||
| chr19:6737516-6737900 | Common:4; Rare:124 | ||||
| chr19:7069640-7069735 | Common:1; Rare:26 | ||||
| chr19:7395037-7395206 | Common:4; Rare:55 | ||||
| chr19:7488997-7489103 | Rare:48 | ||||
| chr19:7534046-7534188 | Common:3; Rare:35; Clinvar (benign):1 | ||||
| chr19:7535631-7535739 | Common:2; Rare:32 | ||||
| chr19:7629523-7629848 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637007-7637143 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr19:7680706-7680869 | Common:1; Rare:52 | ||||
| chr19:7903629-7903912 | Rare:92 | ||||
| chr19:7920213-7920382 | Rare:69 | ||||
| chr19:7943608-7943990 | Rare:112 |