| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38975676-38975876 | Common:1; Rare:49 | ||||
| chr19:39390862-39390948 | Rare:35 | ||||
| chr19:39390978-39391425 | Common:1; Rare:170 | ||||
| chr19:39406706-39406873 | Rare:67 | ||||
| chr19:39412780-39412888 | Rare:21 | ||||
| chr19:39435837-39436188 | Common:8; Rare:134 | ||||
| chr19:39445460-39445834 | Common:2; Rare:103 | ||||
| chr19:39480716-39480955 | Common:3; Rare:118; Clinvar (pathogenic):1 | ||||
| chr19:39846302-39846520 | Common:1; Rare:108 | ||||
| chr19:39970859-39971215 | Common:5; Rare:100 | ||||
| chr19:39996921-39997079 | Common:5; Rare:48 | ||||
| chr19:40056157-40056277 | Rare:18 | ||||
| chr19:40090858-40090999 | Common:1; Rare:39 | ||||
| chr19:40285243-40285627 | Common:3; Rare:132 | ||||
| chr19:40348356-40348746 | Common:4; Rare:127 |