| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49496138-49496470 | Common:1; Rare:114 | ||||
| chr19:49513308-49513403 | Rare:21 | ||||
| chr19:49560353-49560670 | Common:2; Rare:55 | ||||
| chr19:49580528-49580650 | Rare:42 | ||||
| chr19:49665777-49666020 | Common:2; Rare:124; Clinvar (pathogenic):1 | ||||
| chr19:49808757-49808981 | Common:1; Rare:75; Clinvar:1 | ||||
| chr19:49809881-49810148 | Rare:34 | ||||
| chr19:49813257-49813341 | Rare:36 | ||||
| chr19:49850951-49851032 | Common:1; Rare:30 | ||||
| chr19:49851058-49851120 | Rare:24 | ||||
| chr19:49877209-49877726 | Common:2; Rare:129 | ||||
| chr19:49929107-49929204 | Common:3; Rare:34 | ||||
| chr19:49929417-49929567 | Common:4; Rare:54 | ||||
| chr19:49929923-49930219 | Common:1; Rare:70 | ||||
| chr19:50025325-50025711 | Common:7; Rare:126 |