| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48933540-48933696 | Common:3; Rare:40 | ||||
| chr19:48965229-48965609 | Rare:117; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48965762-48966182 | Common:3; Rare:144; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr19:48970662-48970741 | Rare:24 | ||||
| chr19:48993253-48993501 | Common:2; Rare:115; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993553-48993911 | Common:5; Rare:93 | ||||
| chr19:49085126-49085541 | Common:3; Rare:167 | ||||
| chr19:49114250-49114396 | Common:1; Rare:36 | ||||
| chr19:49148608-49148647 | Rare:8 | ||||
| chr19:49155379-49155529 | Rare:26 | ||||
| chr19:49157632-49157835 | Rare:60; Clinvar:1 | ||||
| chr19:49335318-49335490 | Common:1; Rare:35 | ||||
| chr19:49362375-49362525 | Rare:43 | ||||
| chr19:49451735-49452022 | Common:3; Rare:81 | ||||
| chr19:49453094-49453324 | Common:1; Rare:71 |