| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34458502-34458825 | Common:2; Rare:58 | ||||
| chr19:34677227-34677370 | Common:1; Rare:33 | ||||
| chr19:34677595-34677758 | Common:4; Rare:42 | ||||
| chr19:34733802-34733967 | Common:1; Rare:43 | ||||
| chr19:34734177-34734310 | Common:1; Rare:40 | ||||
| chr19:34926823-34927079 | Common:1; Rare:80 | ||||
| chr19:35000178-35000484 | Common:4; Rare:75 | ||||
| chr19:35030412-35030733 | Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:35041555-35041789 | Rare:49 | ||||
| chr19:35115604-35115853 | Common:1; Rare:37 | ||||
| chr19:35138648-35138892 | Rare:61 | ||||
| chr19:35139048-35139165 | Common:2; Rare:27 | ||||
| chr19:35139270-35139675 | Common:3; Rare:78 | ||||
| chr19:35142940-35143275 | Rare:80 | ||||
| chr19:35154651-35154793 | Rare:22 |