| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18152996-18153289 | Common:1; Rare:98 | ||||
| chr19:18433550-18433775 | Common:6; Rare:91 | ||||
| chr19:18539416-18539636 | Common:4; Rare:73 | ||||
| chr19:18571635-18571906 | Common:4; Rare:114 | ||||
| chr19:18573034-18573323 | Common:1; Rare:67 | ||||
| chr19:18598572-18598885 | Common:3; Rare:94; Clinvar (pathogenic):2 | ||||
| chr19:18683445-18683694 | Common:2; Rare:74 | ||||
| chr19:18790906-18791046 | Rare:34; Clinvar:1 | ||||
| chr19:18919316-18919754 | Common:2; Rare:170 | ||||
| chr19:18941233-18941439 | Common:4; Rare:57 | ||||
| chr19:19033462-19033673 | Common:2; Rare:70 | ||||
| chr19:19033831-19033916 | Common:1; Rare:21 | ||||
| chr19:19192110-19192268 | Common:1; Rare:50 | ||||
| chr19:19192614-19192996 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr19:19320476-19320850 | Common:4; Rare:136 |