| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18832684-18832880 | Rare:46 | ||||
| chr19:18895476-18895672 | Common:2; Rare:33 | ||||
| chr19:18895885-18895955 | Rare:13; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:18896042-18896233 | Rare:53; Clinvar:1 | ||||
| chr19:18919024-18919194 | Common:2; Rare:46 | ||||
| chr19:18919305-18919791 | Common:4; Rare:197 | ||||
| chr19:18940288-18940340 | Rare:14 | ||||
| chr19:19033372-19033589 | Common:1; Rare:69 | ||||
| chr19:19033591-19033945 | Common:2; Rare:89 | ||||
| chr19:19034375-19034561 | Common:4; Rare:36 | ||||
| chr19:19063421-19063643 | Common:1; Rare:79 | ||||
| chr19:19063683-19064005 | Rare:108 | ||||
| chr19:19105352-19105518 | Rare:36 | ||||
| chr19:19105558-19105823 | Common:1; Rare:81; Clinvar (pathogenic):1 | ||||
| chr19:19138377-19138638 | Common:3; Rare:80 |