| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18323007-18323165 | Common:1; Rare:64 | ||||
| chr19:18323167-18323317 | Common:2; Rare:39 | ||||
| chr19:18374672-18374717 | Rare:7 | ||||
| chr19:18433258-18433536 | Common:1; Rare:83 | ||||
| chr19:18543455-18543692 | Common:2; Rare:48 | ||||
| chr19:18557680-18557926 | Common:5; Rare:65 | ||||
| chr19:18571578-18571938 | Common:4; Rare:135 | ||||
| chr19:18588629-18588878 | Common:3; Rare:64 | ||||
| chr19:18589929-18590039 | Common:1; Rare:19 | ||||
| chr19:18594346-18594740 | Common:2; Rare:89; Clinvar (pathogenic):1 | ||||
| chr19:18636726-18637060 | Common:2; Rare:83 | ||||
| chr19:18683524-18683705 | Common:1; Rare:62 | ||||
| chr19:18919335-18919856 | Common:3; Rare:197 | ||||
| chr19:18939956-18940336 | Common:2; Rare:96 | ||||
| chr19:18941120-18941436 | Common:4; Rare:101 |