| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38264253-38264585 | Common:6; Rare:85 | ||||
| chr19:38374406-38374812 | Rare:150 | ||||
| chr19:38618849-38619246 | Common:4; Rare:119 | ||||
| chr19:38647378-38647713 | Common:3; Rare:120 | ||||
| chr19:38831762-38831974 | Common:4; Rare:73; Clinvar (benign):1 | ||||
| chr19:38899721-38900029 | Rare:88 | ||||
| chr19:38930726-38930987 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39125537-39125805 | Rare:63 | ||||
| chr19:39342404-39342507 | Common:2; Rare:38 | ||||
| chr19:39390862-39390902 | Rare:17 | ||||
| chr19:39391057-39391418 | Common:1; Rare:149 | ||||
| chr19:39406745-39406847 | Rare:43 | ||||
| chr19:39435854-39436154 | Common:6; Rare:107 | ||||
| chr19:39480756-39480900 | Common:3; Rare:82; Clinvar (pathogenic):1 | ||||
| chr19:39846341-39846479 | Common:1; Rare:62 |