| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9827789-9827963 | Common:1; Rare:65 | ||||
| chr19:10116910-10117151 | Rare:75 | ||||
| chr19:10270994-10271126 | Rare:34 | ||||
| chr19:10315738-10316033 | Common:6; Rare:133; Clinvar (benign):10 | ||||
| chr19:10333503-10333734 | Rare:75 | ||||
| chr19:10380487-10380825 | Common:12; Rare:99; Clinvar:5 | ||||
| chr19:10568972-10569223 | Common:2; Rare:66 | ||||
| chr19:10653833-10653887 | Rare:21 | ||||
| chr19:10836258-10836685 | Common:3; Rare:111 | ||||
| chr19:10928578-10928819 | Common:2; Rare:70 | ||||
| chr19:10960717-10961059 | Common:3; Rare:135 | ||||
| chr19:11089296-11089533 | Rare:44; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11090338-11090590 | Common:2; Rare:71 | ||||
| chr19:11155777-11156048 | Common:3; Rare:62 | ||||
| chr19:11197509-11197622 | Common:1; Rare:30 |