| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38975681-38975845 | Common:1; Rare:37 | ||||
| chr19:39125716-39125839 | Rare:41 | ||||
| chr19:39204126-39204184 | Rare:27 | ||||
| chr19:39204251-39204347 | Rare:23 | ||||
| chr19:39342367-39342545 | Common:2; Rare:61 | ||||
| chr19:39386686-39386874 | Rare:49 | ||||
| chr19:39390827-39391488 | Common:1; Rare:253; Clinvar:1 | ||||
| chr19:39406699-39406946 | Rare:101 | ||||
| chr19:39435838-39436188 | Common:8; Rare:134 | ||||
| chr19:39439645-39439669 | Rare:4 | ||||
| chr19:39445435-39445956 | Common:3; Rare:154 | ||||
| chr19:39480716-39480968 | Common:3; Rare:120; Clinvar (pathogenic):1 | ||||
| chr19:39532806-39532963 | Rare:63 | ||||
| chr19:39540117-39540297 | Common:2; Rare:51 | ||||
| chr19:39830421-39830755 | Rare:123; Clinvar (pathogenic):1 |