| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53090249-53090602 | Rare:48 | ||||
| chr19:53196877-53197164 | Common:11; Rare:57 | ||||
| chr19:54124408-54124564 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr19:54126291-54126612 | Common:1; Rare:96; Clinvar:1 | ||||
| chr19:54136995-54137160 | Common:4; Rare:38 | ||||
| chr19:54179427-54179610 | Rare:25 | ||||
| chr19:54234124-54234347 | Common:6; Rare:27 | ||||
| chr19:54356058-54356159 | Common:1; Rare:23 | ||||
| chr19:54456208-54456408 | Common:1; Rare:83 | ||||
| chr19:54464632-54464673 | Rare:13 | ||||
| chr19:54561915-54561994 | Common:1; Rare:10 | ||||
| chr19:55006049-55006234 | Common:3; Rare:84 | ||||
| chr19:55240944-55241251 | Common:1; Rare:107 | ||||
| chr19:55257663-55257795 | Rare:33 | ||||
| chr19:55503775-55503946 | Common:1; Rare:46 |