| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53869334-53869778 | Common:2; Rare:118 | ||||
| chr19:54102674-54102887 | Common:3; Rare:56 | ||||
| chr19:54115259-54115425 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr19:54115628-54115795 | Common:1; Rare:41; Clinvar:4 | ||||
| chr19:54200685-54200898 | Common:3; Rare:85 | ||||
| chr19:54449039-54449247 | Common:2; Rare:60 | ||||
| chr19:55370439-55370605 | Rare:30 | ||||
| chr19:55385737-55385982 | Common:6; Rare:84 | ||||
| chr19:56368268-56368354 | Common:2; Rare:30 | ||||
| chr19:56404259-56404355 | Common:1; Rare:26 | ||||
| chr19:56477828-56478249 | Common:6; Rare:124 | ||||
| chr19:57279685-57279995 | Common:1; Rare:69 | ||||
| chr19:57280293-57280510 | Common:1; Rare:70 | ||||
| chr19:57435142-57435349 | Common:6; Rare:43 | ||||
| chr19:57916580-57916858 | Common:2; Rare:97 |