| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033803-19033914 | Common:1; Rare:29 | ||||
| chr19:19192115-19192286 | Common:1; Rare:53 | ||||
| chr19:19192624-19192975 | Common:2; Rare:83 | ||||
| chr19:19320480-19320850 | Common:4; Rare:133 | ||||
| chr19:19516167-19516295 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19821674-19821905 | Common:1; Rare:80 | ||||
| chr19:19900778-19900958 | Rare:43 | ||||
| chr19:20661524-20661755 | Common:7; Rare:66 | ||||
| chr19:20923119-20923334 | Rare:58 | ||||
| chr19:21020517-21020688 | Common:3; Rare:32 | ||||
| chr19:21141823-21142087 | Rare:75 | ||||
| chr19:21329296-21329492 | Common:2; Rare:44 | ||||
| chr19:21396951-21397173 | Rare:59 | ||||
| chr19:21505539-21505654 | Common:1; Rare:31 | ||||
| chr19:22784119-22784297 | Rare:44 |