| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033777-19033925 | Common:1; Rare:40 | ||||
| chr19:19033984-19034015 | Rare:4 | ||||
| chr19:19105674-19105810 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr19:19192104-19192274 | Common:1; Rare:52 | ||||
| chr19:19192559-19193056 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr19:19320472-19320858 | Common:4; Rare:145 | ||||
| chr19:19385900-19386053 | Rare:58 | ||||
| chr19:19516145-19516331 | Rare:117; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19528158-19528397 | Rare:49 | ||||
| chr19:19668537-19668977 | Common:3; Rare:128 | ||||
| chr19:19821638-19821905 | Common:1; Rare:90 | ||||
| chr19:19900795-19900998 | Common:1; Rare:52 | ||||
| chr19:20039186-20039313 | Common:1; Rare:28 | ||||
| chr19:20077818-20078045 | Common:2; Rare:67 | ||||
| chr19:20167061-20167347 | Common:2; Rare:113 |