| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17419680-17420134 | Common:21; Rare:126 | ||||
| chr19:17448649-17448788 | Rare:36 | ||||
| chr19:17470158-17470436 | Common:1; Rare:72 | ||||
| chr19:17511320-17511745 | Common:3; Rare:138 | ||||
| chr19:17511793-17512404 | Common:2; Rare:193 | ||||
| chr19:17539633-17539685 | Rare:13 | ||||
| chr19:17539696-17540068 | Common:3; Rare:122 | ||||
| chr19:17555456-17555728 | Common:1; Rare:78 | ||||
| chr19:17555770-17555936 | Common:1; Rare:52 | ||||
| chr19:17688319-17688442 | Common:2; Rare:34 | ||||
| chr19:17719354-17719579 | Common:3; Rare:83 | ||||
| chr19:17842049-17842379 | Common:1; Rare:87; Clinvar:1 | ||||
| chr19:17842488-17842569 | Rare:28; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:17847566-17847792 | Common:2; Rare:83 | ||||
| chr19:17847946-17848157 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 |