| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12400225-12400524 | Rare:60 | ||||
| chr19:12400757-12400974 | Rare:76 | ||||
| chr19:12401098-12401385 | Common:2; Rare:90 | ||||
| chr19:12440944-12441204 | Common:5; Rare:79 | ||||
| chr19:12484716-12484919 | Rare:53 | ||||
| chr19:12550993-12551138 | Common:4; Rare:36 | ||||
| chr19:12551151-12551525 | Common:2; Rare:128 | ||||
| chr19:12551527-12551928 | Common:2; Rare:78 | ||||
| chr19:12610618-12610995 | Rare:120 | ||||
| chr19:12611391-12611546 | Common:2; Rare:33 | ||||
| chr19:12666684-12666874 | Rare:77; Clinvar:4 | ||||
| chr19:12668940-12669215 | Common:1; Rare:77 | ||||
| chr19:12669359-12669782 | Common:5; Rare:154 | ||||
| chr19:12681181-12682097 | Common:6; Rare:372; Clinvar (pathogenic):1 | ||||
| chr19:12696182-12696288 | Common:1; Rare:41 |