| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9675022-9675207 | Common:1; Rare:52 | ||||
| chr19:9768588-9768819 | Common:3; Rare:79 | ||||
| chr19:9818800-9818868 | Rare:27 | ||||
| chr19:9827823-9827963 | Common:1; Rare:53 | ||||
| chr19:9835013-9835372 | Rare:149 | ||||
| chr19:10116918-10117153 | Rare:75 | ||||
| chr19:10231265-10231335 | Rare:16 | ||||
| chr19:10251751-10252002 | Common:1; Rare:61 | ||||
| chr19:10315919-10316264 | Common:4; Rare:120; Clinvar (benign):8 | ||||
| chr19:10333504-10333712 | Rare:69 | ||||
| chr19:10653833-10653887 | Rare:21 | ||||
| chr19:10836277-10836571 | Common:2; Rare:77 | ||||
| chr19:10928599-10928802 | Common:2; Rare:55 | ||||
| chr19:10960686-10961059 | Common:3; Rare:149 | ||||
| chr19:11089300-11089539 | Rare:49; Clinvar:12; Clinvar (pathogenic):1 |