| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45642090-45642540 | Common:3; Rare:242 | ||||
| chr19:45667950-45668270 | Common:2; Rare:56 | ||||
| chr19:45677180-45677770 | Common:8; Rare:294 | ||||
| chr19:45691798-45692110 | Rare:250 | ||||
| chr19:45692165-45692796 | Common:7; Rare:342 | ||||
| chr19:45730811-45731184 | Common:3; Rare:189 | ||||
| chr19:45768193-45768592 | Rare:351; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr19:45768708-45768966 | Common:3; Rare:170; Clinvar:1; Clinvar (benign):6 | ||||
| chr19:45769006-45769748 | Common:6; Rare:550 | ||||
| chr19:45770560-45770982 | Common:8; Rare:326; Clinvar:1 | ||||
| chr19:45779160-45779820 | Common:5; Rare:282 | ||||
| chr19:45791510-45792189 | Common:3; Rare:185 | ||||
| chr19:45792692-45793133 | Common:7; Rare:189 | ||||
| chr19:45862110-45862780 | Common:6; Rare:232 | ||||
| chr19:45863035-45863420 | Common:14; Rare:338 |