| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44500477-44500649 | Common:3; Rare:52 | ||||
| chr19:44914495-44914726 | Rare:56 | ||||
| chr19:44955217-44955410 | Common:2; Rare:53 | ||||
| chr19:45038941-45039094 | Rare:52 | ||||
| chr19:45079173-45079331 | Rare:46 | ||||
| chr19:45091579-45091828 | Common:2; Rare:63 | ||||
| chr19:45092809-45092956 | Common:2; Rare:44 | ||||
| chr19:45370550-45370799 | Common:2; Rare:73 | ||||
| chr19:45406341-45406682 | Common:2; Rare:84 | ||||
| chr19:45423488-45423696 | Common:2; Rare:45; Clinvar (benign):1 | ||||
| chr19:45423816-45423993 | Common:2; Rare:37 | ||||
| chr19:45496954-45497278 | Common:3; Rare:96 | ||||
| chr19:45499528-45499709 | Rare:59 | ||||
| chr19:45507226-45507499 | Common:1; Rare:68 | ||||
| chr19:45584776-45585041 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):4 |