| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49928608-49928825 | Common:2; Rare:45 | ||||
| chr19:49928959-49929285 | Common:3; Rare:102 | ||||
| chr19:49929324-49929820 | Common:7; Rare:166 | ||||
| chr19:50025331-50025732 | Common:7; Rare:132 | ||||
| chr19:50415443-50415825 | Common:2; Rare:122; Clinvar:38; Clinvar (benign):35 | ||||
| chr19:50476419-50476550 | Rare:56 | ||||
| chr19:50476723-50476806 | Rare:16 | ||||
| chr19:50511060-50511616 | Common:5; Rare:188 | ||||
| chr19:50658137-50658573 | Common:1; Rare:93 | ||||
| chr19:50804214-50804258 | Common:1; Rare:17 | ||||
| chr19:50804570-50804751 | Common:5; Rare:64 | ||||
| chr19:50804924-50805106 | Common:2; Rare:52 | ||||
| chr19:51339688-51340027 | Common:1; Rare:68 | ||||
| chr19:51357461-51357756 | Common:4; Rare:52 | ||||
| chr19:51366269-51366609 | Common:8; Rare:105; Clinvar (benign):2 |