| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49114128-49114407 | Common:4; Rare:70 | ||||
| chr19:49119074-49119278 | Rare:67 | ||||
| chr19:49119621-49119712 | Common:1; Rare:22 | ||||
| chr19:49335224-49335459 | Common:1; Rare:40 | ||||
| chr19:49362363-49362473 | Rare:30 | ||||
| chr19:49451748-49452006 | Common:3; Rare:68 | ||||
| chr19:49452981-49453300 | Common:3; Rare:92 | ||||
| chr19:49453473-49453639 | Common:1; Rare:48 | ||||
| chr19:49513130-49513403 | Common:1; Rare:67 | ||||
| chr19:49580534-49580686 | Rare:47 | ||||
| chr19:49581255-49581434 | Common:1; Rare:36 | ||||
| chr19:49590156-49590367 | Common:2; Rare:79 | ||||
| chr19:49665588-49666038 | Common:6; Rare:206; Clinvar (pathogenic):1 | ||||
| chr19:49851058-49851120 | Rare:24 | ||||
| chr19:49877277-49877724 | Common:1; Rare:116 |