| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:33521747-33521948 | Rare:65; Clinvar:5 | ||||
| chr19:33795828-33796091 | Common:4; Rare:74 | ||||
| chr19:33796256-33796490 | Common:3; Rare:68 | ||||
| chr19:34172363-34172757 | Common:1; Rare:135 | ||||
| chr19:34207869-34207898 | Rare:3 | ||||
| chr19:34254489-34254606 | Rare:37 | ||||
| chr19:34365066-34365292 | Common:1; Rare:99 | ||||
| chr19:34399692-34400048 | Rare:109; Clinvar (pathogenic):2 | ||||
| chr19:34404288-34404436 | Common:2; Rare:57 | ||||
| chr19:34428316-34428541 | Rare:78 | ||||
| chr19:34677208-34677762 | Common:8; Rare:145 | ||||
| chr19:34733845-34734210 | Common:2; Rare:94 | ||||
| chr19:34734458-34734589 | Rare:28 | ||||
| chr19:34926823-34926976 | Common:1; Rare:55 | ||||
| chr19:35000221-35000475 | Common:4; Rare:66 |