| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48993274-48993566 | Common:3; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:49085088-49085492 | Common:3; Rare:156 | ||||
| chr19:49362375-49362497 | Rare:36 | ||||
| chr19:49453094-49453290 | Common:1; Rare:59 | ||||
| chr19:49487258-49487582 | Common:4; Rare:105 | ||||
| chr19:49496276-49496470 | Common:1; Rare:74 | ||||
| chr19:49580534-49580742 | Common:1; Rare:55 | ||||
| chr19:49665761-49666023 | Common:3; Rare:128; Clinvar (pathogenic):1 | ||||
| chr19:49690978-49691159 | Common:2; Rare:41 | ||||
| chr19:49851058-49851140 | Rare:30 | ||||
| chr19:49867546-49867686 | Common:3; Rare:37 | ||||
| chr19:49877319-49877717 | Common:1; Rare:99 | ||||
| chr19:49877836-49878141 | Common:5; Rare:95 | ||||
| chr19:49929408-49929567 | Common:4; Rare:58 | ||||
| chr19:49929922-49930219 | Common:1; Rare:71 |