| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49527856-49528019 | Common:3; Rare:50 | ||||
| chr19:49580518-49580653 | Rare:47 | ||||
| chr19:49639954-49640593 | Common:1; Rare:187; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49662289-49662471 | Common:1; Rare:64 | ||||
| chr19:49665374-49666027 | Common:6; Rare:278; Clinvar (pathogenic):1 | ||||
| chr19:49690989-49691151 | Common:2; Rare:40 | ||||
| chr19:49712709-49712773 | Rare:15 | ||||
| chr19:49817319-49817631 | Common:3; Rare:65 | ||||
| chr19:49851045-49851182 | Common:1; Rare:55 | ||||
| chr19:49854380-49855072 | Common:7; Rare:274 | ||||
| chr19:49857539-49857992 | Common:4; Rare:187 | ||||
| chr19:49860089-49860449 | Common:3; Rare:150 | ||||
| chr19:49876190-49876283 | Rare:33 | ||||
| chr19:49876585-49876747 | Common:1; Rare:63 | ||||
| chr19:49877185-49877729 | Common:2; Rare:134 |