| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18323034-18323348 | Common:3; Rare:105 | ||||
| chr19:18340491-18340646 | Common:4; Rare:61 | ||||
| chr19:18542871-18543034 | Rare:47 | ||||
| chr19:18557687-18557911 | Common:4; Rare:59 | ||||
| chr19:18571660-18571906 | Common:3; Rare:107 | ||||
| chr19:18594391-18594509 | Common:1; Rare:32 | ||||
| chr19:18683473-18683699 | Common:1; Rare:74 | ||||
| chr19:18919335-18919783 | Common:3; Rare:172 | ||||
| chr19:18941239-18941523 | Common:4; Rare:69 | ||||
| chr19:19033452-19033649 | Common:2; Rare:67 | ||||
| chr19:19033798-19033935 | Common:1; Rare:36 | ||||
| chr19:19192110-19192242 | Common:1; Rare:41 | ||||
| chr19:19192582-19192996 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr19:19211818-19212028 | Rare:54 | ||||
| chr19:19516167-19516331 | Rare:95; Clinvar:1; Clinvar (pathogenic):1 |