| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49155367-49155529 | Rare:28 | ||||
| chr19:49157640-49157842 | Rare:59; Clinvar:1 | ||||
| chr19:49335253-49335478 | Common:1; Rare:39 | ||||
| chr19:49357274-49357567 | Common:1; Rare:69 | ||||
| chr19:49453084-49453313 | Common:1; Rare:75 | ||||
| chr19:49453472-49453635 | Common:1; Rare:47 | ||||
| chr19:49474479-49474606 | Rare:29 | ||||
| chr19:49487282-49487644 | Common:5; Rare:130 | ||||
| chr19:49512363-49512763 | Common:1; Rare:75 | ||||
| chr19:49513108-49513466 | Common:1; Rare:77 | ||||
| chr19:49513692-49514114 | Common:9; Rare:105 | ||||
| chr19:49527864-49528038 | Common:3; Rare:53 | ||||
| chr19:49580521-49580650 | Rare:46 | ||||
| chr19:49641834-49642077 | Rare:69 | ||||
| chr19:49665609-49666027 | Common:6; Rare:198; Clinvar (pathogenic):1 |