| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50383971-50384425 | Common:4; Rare:187; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:50384540-50384693 | Rare:37 | ||||
| chr19:50415760-50415953 | Rare:58; Clinvar:13; Clinvar (benign):9 | ||||
| chr19:50418230-50418541 | Common:3; Rare:85 | ||||
| chr19:50418782-50419045 | Rare:95 | ||||
| chr19:50476322-50476617 | Rare:127 | ||||
| chr19:50476719-50476911 | Rare:51 | ||||
| chr19:50511072-50511598 | Common:5; Rare:171 | ||||
| chr19:50803974-50804306 | Common:5; Rare:104 | ||||
| chr19:50804481-50804916 | Common:9; Rare:149 | ||||
| chr19:50804920-50805171 | Common:5; Rare:66 | ||||
| chr19:50820313-50820574 | Common:2; Rare:59; Clinvar:1 | ||||
| chr19:50820796-50820991 | Common:1; Rare:36 | ||||
| chr19:50821015-50821168 | Rare:36 | ||||
| chr19:51107956-51108188 | Common:1; Rare:46 |