| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10568971-10569298 | Common:2; Rare:83 | ||||
| chr19:10569470-10569890 | Common:2; Rare:68 | ||||
| chr19:10602287-10602535 | Rare:74 | ||||
| chr19:10602685-10602881 | Common:3; Rare:35 | ||||
| chr19:10625318-10625595 | Common:3; Rare:66 | ||||
| chr19:10653808-10654003 | Common:1; Rare:74 | ||||
| chr19:10701276-10701502 | Rare:78 | ||||
| chr19:10701633-10702033 | Common:1; Rare:112 | ||||
| chr19:10836196-10836371 | Common:1; Rare:49 | ||||
| chr19:10836430-10836640 | Common:1; Rare:50 | ||||
| chr19:10871552-10872464 | Common:8; Rare:353 | ||||
| chr19:10928636-10928875 | Common:1; Rare:82 | ||||
| chr19:10960613-10960904 | Common:7; Rare:111 | ||||
| chr19:10960940-10961310 | Rare:135; Clinvar (benign):2 | ||||
| chr19:11089223-11089529 | Rare:49; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):2 |