| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48993757-48993920 | Common:4; Rare:53 | ||||
| chr19:49085118-49085525 | Common:3; Rare:167 | ||||
| chr19:49451754-49451991 | Common:3; Rare:60 | ||||
| chr19:49580529-49580679 | Rare:49 | ||||
| chr19:49665761-49666034 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49818224-49818339 | Common:4; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49929922-49930219 | Common:1; Rare:71 | ||||
| chr19:51366321-51366562 | Common:5; Rare:69; Clinvar (benign):2 | ||||
| chr19:52189819-52190088 | Common:3; Rare:115 | ||||
| chr19:52269475-52269603 | Common:1; Rare:50 | ||||
| chr19:52297009-52297198 | Common:18; Rare:45 | ||||
| chr19:52397755-52397907 | Common:4; Rare:50 | ||||
| chr19:52638332-52638541 | Common:4; Rare:54 | ||||
| chr19:53132876-53132934 | Common:2; Rare:18 | ||||
| chr19:53869438-53869669 | Common:1; Rare:63 |