| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38899491-38900033 | Rare:163 | ||||
| chr19:38900149-38900305 | Common:1; Rare:35 | ||||
| chr19:38930318-38930575 | Common:1; Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:38930671-38931094 | Common:4; Rare:124; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:39125558-39125856 | Common:1; Rare:77 | ||||
| chr19:39335175-39335392 | Common:1; Rare:53 | ||||
| chr19:39335654-39335829 | Common:2; Rare:38 | ||||
| chr19:39335972-39336194 | Rare:60 | ||||
| chr19:39341897-39342047 | Rare:34 | ||||
| chr19:39390961-39391508 | Common:1; Rare:208 | ||||
| chr19:39391638-39391713 | Rare:23 | ||||
| chr19:39406684-39407034 | Rare:124 | ||||
| chr19:39407133-39407370 | Rare:45 | ||||
| chr19:39412205-39412761 | Common:3; Rare:222 | ||||
| chr19:39412777-39412917 | Common:1; Rare:26 |