| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:8544290-8544660 | Common:5; Rare:111; Clinvar (benign):1 | ||||
| chr19:8569543-8569757 | Common:1; Rare:38 | ||||
| chr19:10284505-10284952 | Common:5; Rare:132 | ||||
| chr19:10603437-10603610 | Rare:38 | ||||
| chr19:11321317-11321562 | Rare:61 | ||||
| chr19:12779722-12779888 | Common:2; Rare:39 | ||||
| chr19:12790211-12790376 | Common:1; Rare:38 | ||||
| chr19:12793496-12793760 | Common:3; Rare:74 | ||||
| chr19:13104338-13104582 | Rare:58 | ||||
| chr19:13104613-13104758 | Common:1; Rare:34 | ||||
| chr19:13105594-13105763 | Rare:46 | ||||
| chr19:13167371-13167742 | Common:2; Rare:82 | ||||
| chr19:13839259-13839338 | Common:1; Rare:12 | ||||
| chr19:13840678-13840896 | Common:1; Rare:43 | ||||
| chr19:14155192-14155227 | Rare:9 |