| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10086230-10086372 | Rare:38 | ||||
| chr19:10116847-10117151 | Rare:83 | ||||
| chr19:10194892-10195197 | Common:1; Rare:132; Clinvar (benign):2 | ||||
| chr19:10270364-10270404 | Rare:6 | ||||
| chr19:10270813-10271172 | Common:2; Rare:100 | ||||
| chr19:10333484-10333709 | Common:1; Rare:78 | ||||
| chr19:10380487-10380817 | Common:12; Rare:95; Clinvar:5 | ||||
| chr19:10395027-10395242 | Rare:62 | ||||
| chr19:10403383-10403965 | Rare:185 | ||||
| chr19:10502702-10502909 | Rare:53 | ||||
| chr19:10568972-10569094 | Common:2; Rare:36 | ||||
| chr19:10577203-10577503 | Common:2; Rare:79 | ||||
| chr19:10653795-10653881 | Rare:37 | ||||
| chr19:10836191-10836251 | Rare:16 | ||||
| chr19:10836258-10836558 | Common:2; Rare:75 |