| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45451099-45451229 | Common:1; Rare:21 | ||||
| chr19:45467561-45467771 | Common:1; Rare:63 | ||||
| chr19:45467888-45468035 | Rare:45 | ||||
| chr19:45469147-45469538 | Common:2; Rare:124 | ||||
| chr19:45469703-45469935 | Common:3; Rare:66 | ||||
| chr19:45478616-45478698 | Rare:50 | ||||
| chr19:45492691-45492906 | Common:1; Rare:51 | ||||
| chr19:45493200-45493477 | Rare:84; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:45496933-45497306 | Common:3; Rare:108 | ||||
| chr19:45498507-45498693 | Rare:67 | ||||
| chr19:45506519-45506744 | Common:1; Rare:64 | ||||
| chr19:45506797-45506985 | Common:1; Rare:58 | ||||
| chr19:45507225-45507526 | Common:1; Rare:82 | ||||
| chr19:45507756-45507890 | Rare:49 | ||||
| chr19:45584187-45584646 | Common:3; Rare:130; Clinvar:1 |