| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38647593-38647864 | Rare:98 | ||||
| chr19:38723649-38723988 | Common:1; Rare:85 | ||||
| chr19:38831722-38832040 | Common:4; Rare:109; Clinvar (benign):1 | ||||
| chr19:38852319-38852488 | Rare:43 | ||||
| chr19:38899528-38900079 | Rare:165 | ||||
| chr19:38930737-38931013 | Common:3; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975681-38975844 | Common:1; Rare:36 | ||||
| chr19:39390850-39391011 | Rare:53 | ||||
| chr19:39391025-39391442 | Common:1; Rare:170 | ||||
| chr19:39406673-39406940 | Rare:99 | ||||
| chr19:39406952-39407109 | Rare:33 | ||||
| chr19:39412261-39412587 | Common:2; Rare:149 | ||||
| chr19:39412795-39412854 | Rare:12 | ||||
| chr19:39435854-39436305 | Common:9; Rare:166 | ||||
| chr19:39445426-39445829 | Common:2; Rare:122 |