| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35000170-35000484 | Common:4; Rare:76 | ||||
| chr19:35022944-35023324 | Common:1; Rare:76 | ||||
| chr19:35041064-35041315 | Common:2; Rare:49 | ||||
| chr19:35142967-35143275 | Rare:69 | ||||
| chr19:35154591-35154857 | Rare:46 | ||||
| chr19:35155132-35155230 | Rare:20 | ||||
| chr19:35155333-35155609 | Rare:75 | ||||
| chr19:35248873-35249034 | Common:1; Rare:71 | ||||
| chr19:35266946-35267257 | Common:1; Rare:111 | ||||
| chr19:35268431-35268546 | Rare:15 | ||||
| chr19:35268975-35269162 | Common:1; Rare:25 | ||||
| chr19:35329058-35329279 | Rare:45 | ||||
| chr19:35545454-35545689 | Common:4; Rare:80 | ||||
| chr19:35628878-35629171 | Common:4; Rare:87 | ||||
| chr19:35648110-35648402 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 |