| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9768567-9768761 | Common:2; Rare:69 | ||||
| chr19:9818811-9818864 | Rare:22 | ||||
| chr19:9827810-9827971 | Common:1; Rare:61 | ||||
| chr19:10119656-10119927 | Common:2; Rare:110 | ||||
| chr19:10270973-10271133 | Rare:44 | ||||
| chr19:10333465-10333719 | Common:1; Rare:94 | ||||
| chr19:10396035-10396492 | Common:1; Rare:106 | ||||
| chr19:10552113-10552280 | Rare:65 | ||||
| chr19:10568961-10569206 | Common:2; Rare:64 | ||||
| chr19:10653817-10653899 | Rare:31 | ||||
| chr19:10798392-10798572 | Rare:58; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:10836187-10836280 | Rare:28 | ||||
| chr19:10928529-10928806 | Common:2; Rare:78 | ||||
| chr19:10960686-10961117 | Common:3; Rare:168 | ||||
| chr19:11090283-11090618 | Common:2; Rare:98 |