| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58347470-58347890 | Common:8; Rare:166 | ||||
| chr19:58362427-58362631 | Common:1; Rare:59 | ||||
| chr19:58362815-58363024 | Common:1; Rare:59 | ||||
| chr19:58380683-58380859 | Common:1; Rare:37 | ||||
| chr19:58381000-58381227 | Common:4; Rare:46 | ||||
| chr19:58386620-58386930 | Common:3; Rare:84 | ||||
| chr19:58387089-58387325 | Common:1; Rare:89 | ||||
| chr19:58401200-58401589 | Common:6; Rare:122 | ||||
| chr19:58408371-58408778 | Common:5; Rare:133 | ||||
| chr19:58440110-58440508 | Common:6; Rare:105 | ||||
| chr19:58451408-58451682 | Common:5; Rare:108 | ||||
| chr19:58466838-58467119 | Common:1; Rare:88 | ||||
| chr19:58475580-58476450 | Common:7; Rare:321 | ||||
| chr19:58499216-58499571 | Common:2; Rare:115; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:58519050-58519196 | Rare:36 |