| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38647611-38647919 | Rare:96 | ||||
| chr19:38723610-38723989 | Common:1; Rare:102 | ||||
| chr19:38724253-38724562 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:38812934-38813280 | Common:2; Rare:62 | ||||
| chr19:38815644-38816024 | Common:2; Rare:134; Clinvar (benign):1 | ||||
| chr19:38831702-38832061 | Common:5; Rare:119; Clinvar (benign):1 | ||||
| chr19:38842415-38842587 | Rare:39 | ||||
| chr19:38852319-38852532 | Rare:49 | ||||
| chr19:38878241-38878352 | Rare:16 | ||||
| chr19:38899533-38900033 | Rare:152 | ||||
| chr19:38930688-38931002 | Common:3; Rare:96; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:38975674-38975866 | Common:1; Rare:48 | ||||
| chr19:39335983-39336186 | Rare:55 | ||||
| chr19:39386701-39386913 | Rare:51 | ||||
| chr19:39389102-39389459 | Common:1; Rare:83 |