| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11381172-11381484 | Common:2; Rare:100; Clinvar:1 | ||||
| chr19:11419294-11419449 | Rare:30 | ||||
| chr19:11435517-11435694 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11529077-11529291 | Rare:41 | ||||
| chr19:11559190-11559449 | Common:3; Rare:81 | ||||
| chr19:12551421-12551726 | Common:2; Rare:85 | ||||
| chr19:12610723-12610989 | Rare:91 | ||||
| chr19:12666697-12666844 | Rare:58; Clinvar:4 | ||||
| chr19:12681362-12681569 | Common:2; Rare:81 | ||||
| chr19:12681761-12681962 | Common:2; Rare:102; Clinvar (pathogenic):1 | ||||
| chr19:12696582-12696727 | Rare:68 | ||||
| chr19:12722617-12722869 | Common:1; Rare:54 | ||||
| chr19:12723851-12724031 | Common:1; Rare:49 | ||||
| chr19:12734329-12734490 | Rare:38 | ||||
| chr19:12734497-12734887 | Common:1; Rare:137 |