| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18153012-18153287 | Common:1; Rare:95 | ||||
| chr19:18203923-18204366 | Common:2; Rare:138 | ||||
| chr19:18280211-18280450 | Common:4; Rare:92 | ||||
| chr19:18323034-18323302 | Common:3; Rare:85 | ||||
| chr19:18340507-18340646 | Common:3; Rare:54 | ||||
| chr19:18557668-18557892 | Common:5; Rare:57 | ||||
| chr19:18571629-18571906 | Common:4; Rare:114 | ||||
| chr19:18683481-18683694 | Common:1; Rare:69 | ||||
| chr19:18919323-18919738 | Common:2; Rare:153 | ||||
| chr19:19033446-19033686 | Common:2; Rare:81 | ||||
| chr19:19033803-19033930 | Common:1; Rare:35 | ||||
| chr19:19192113-19192264 | Common:1; Rare:48 | ||||
| chr19:19192624-19193008 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr19:19320480-19320760 | Common:3; Rare:92 | ||||
| chr19:19516157-19516292 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 |