| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18340534-18340644 | Common:2; Rare:42 | ||||
| chr19:18557648-18557898 | Common:5; Rare:68 | ||||
| chr19:18571606-18571900 | Common:3; Rare:113 | ||||
| chr19:18588593-18588831 | Common:4; Rare:53 | ||||
| chr19:18683469-18683688 | Common:2; Rare:66 | ||||
| chr19:18919352-18919738 | Common:2; Rare:131 | ||||
| chr19:19033458-19033646 | Common:2; Rare:65 | ||||
| chr19:19170228-19170443 | Common:2; Rare:53 | ||||
| chr19:19192118-19192233 | Common:1; Rare:38 | ||||
| chr19:19192574-19192969 | Common:2; Rare:104 | ||||
| chr19:19320480-19320850 | Common:4; Rare:133 | ||||
| chr19:19516147-19516285 | Rare:91; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19643569-19643723 | Common:3; Rare:48 | ||||
| chr19:19663556-19663759 | Rare:71 | ||||
| chr19:19668248-19668451 | Common:1; Rare:39 |