| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18203967-18204366 | Common:2; Rare:122 | ||||
| chr19:18323025-18323302 | Common:3; Rare:89 | ||||
| chr19:18340518-18340646 | Common:3; Rare:48 | ||||
| chr19:18542896-18543008 | Rare:36 | ||||
| chr19:18557668-18557898 | Common:5; Rare:58 | ||||
| chr19:18571654-18571891 | Common:2; Rare:97 | ||||
| chr19:18588682-18588862 | Rare:46 | ||||
| chr19:18683469-18683691 | Common:2; Rare:67 | ||||
| chr19:18919352-18919740 | Common:2; Rare:133 | ||||
| chr19:18941239-18941478 | Common:4; Rare:56 | ||||
| chr19:19033448-19033649 | Common:2; Rare:68 | ||||
| chr19:19033803-19033882 | Rare:20 | ||||
| chr19:19105720-19105852 | Common:1; Rare:43; Clinvar (pathogenic):1 | ||||
| chr19:19192124-19192268 | Common:1; Rare:45 | ||||
| chr19:19192624-19192976 | Common:2; Rare:83 |