| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37907045-37907293 | Rare:54 | ||||
| chr19:38264366-38264585 | Common:2; Rare:60 | ||||
| chr19:38264791-38264904 | Rare:43 | ||||
| chr19:38374407-38374812 | Rare:149 | ||||
| chr19:38618814-38619310 | Common:4; Rare:141 | ||||
| chr19:38723634-38723972 | Common:1; Rare:87 | ||||
| chr19:38831721-38832045 | Common:4; Rare:110; Clinvar (benign):1 | ||||
| chr19:38852319-38852435 | Rare:32 | ||||
| chr19:38899528-38899959 | Rare:123 | ||||
| chr19:38930738-38930992 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975667-38975845 | Common:1; Rare:41 | ||||
| chr19:39390984-39391425 | Common:1; Rare:168 | ||||
| chr19:39406706-39406889 | Rare:76 | ||||
| chr19:39423621-39423857 | Common:3; Rare:88; Clinvar (benign):1 | ||||
| chr19:39435854-39436163 | Common:6; Rare:112 |