| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49451748-49452002 | Common:3; Rare:66 | ||||
| chr19:49453094-49453244 | Common:1; Rare:47 | ||||
| chr19:49453452-49453588 | Rare:45 | ||||
| chr19:49474120-49474266 | Common:1; Rare:32 | ||||
| chr19:49487278-49487649 | Common:5; Rare:132 | ||||
| chr19:49496128-49496470 | Common:1; Rare:116 | ||||
| chr19:49580521-49580733 | Common:1; Rare:63 | ||||
| chr19:49665609-49666023 | Common:6; Rare:195; Clinvar (pathogenic):1 | ||||
| chr19:49818239-49818372 | Common:3; Rare:65; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49877291-49877717 | Common:1; Rare:107 | ||||
| chr19:49877922-49878158 | Common:2; Rare:75 | ||||
| chr19:49929063-49929212 | Common:3; Rare:48 | ||||
| chr19:49929404-49929425 | Rare:7 | ||||
| chr19:49929430-49929531 | Common:1; Rare:35 | ||||
| chr19:50432686-50432916 | Common:3; Rare:51 |