| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18542900-18543161 | Common:1; Rare:57 | ||||
| chr19:18557741-18557909 | Common:3; Rare:46 | ||||
| chr19:18571638-18571891 | Common:3; Rare:102 | ||||
| chr19:18683524-18683714 | Common:1; Rare:65 | ||||
| chr19:18919343-18919783 | Common:3; Rare:165 | ||||
| chr19:18941239-18941559 | Common:4; Rare:76 | ||||
| chr19:19033437-19033649 | Common:2; Rare:73 | ||||
| chr19:19033803-19033922 | Common:1; Rare:34 | ||||
| chr19:19105711-19105850 | Common:1; Rare:47; Clinvar (pathogenic):1 | ||||
| chr19:19192115-19192268 | Common:1; Rare:50 | ||||
| chr19:19192556-19192996 | Common:3; Rare:116; Clinvar (benign):1 | ||||
| chr19:19273288-19273450 | Rare:38 | ||||
| chr19:19320476-19320857 | Common:4; Rare:140 | ||||
| chr19:19516157-19516306 | Rare:90; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19628517-19628689 | Rare:29 |