| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5293167-5293450 | Common:1; Rare:118 | ||||
| chr19:5622708-5623213 | Common:5; Rare:203 | ||||
| chr19:5623245-5623342 | Common:1; Rare:32 | ||||
| chr19:5680154-5680301 | Rare:56 | ||||
| chr19:5680481-5680772 | Rare:86 | ||||
| chr19:5680892-5681176 | Rare:84 | ||||
| chr19:5708226-5708380 | Common:1; Rare:46 | ||||
| chr19:5719765-5720337 | Common:2; Rare:230; Clinvar:1 | ||||
| chr19:5787349-5787688 | Common:2; Rare:105 | ||||
| chr19:5790507-5790561 | Common:1; Rare:13 | ||||
| chr19:5791125-5791246 | Common:3; Rare:48 | ||||
| chr19:5903432-5903845 | Common:2; Rare:140; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr19:5978066-5978413 | Common:3; Rare:134 | ||||
| chr19:6110447-6110705 | Rare:79 | ||||
| chr19:6361510-6362013 | Common:3; Rare:201; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 |