| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48807311-48807377 | Common:1; Rare:13 | ||||
| chr19:48811004-48811136 | Rare:45 | ||||
| chr19:48868553-48868753 | Common:1; Rare:37 | ||||
| chr19:48965246-48965916 | Common:1; Rare:230; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chr19:48993290-48993508 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:48993553-48993921 | Common:5; Rare:96 | ||||
| chr19:49085123-49085531 | Common:3; Rare:165 | ||||
| chr19:49335159-49335462 | Common:1; Rare:51 | ||||
| chr19:49451745-49452002 | Common:3; Rare:67 | ||||
| chr19:49453039-49453318 | Common:1; Rare:88 | ||||
| chr19:49453473-49453588 | Rare:31 | ||||
| chr19:49513124-49513465 | Common:1; Rare:75 | ||||
| chr19:49580528-49580687 | Rare:51 | ||||
| chr19:49665777-49666029 | Common:2; Rare:130; Clinvar (pathogenic):1 | ||||
| chr19:49851058-49851140 | Rare:30 |