| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49929366-49929926 | Common:20; Rare:482 | ||||
| chr19:50025285-50025752 | Common:21; Rare:420 | ||||
| chr19:50025861-50026129 | Common:1; Rare:72 | ||||
| chr19:50203298-50203729 | Common:7; Rare:274; Clinvar:4; Clinvar (benign):3 | ||||
| chr19:50328930-50329769 | Common:9; Rare:539; Clinvar:3; Clinvar (benign):7 | ||||
| chr19:50333354-50333720 | Common:7; Rare:149 | ||||
| chr19:50376002-50376633 | Common:14; Rare:231 | ||||
| chr19:50376580-50377050 | Common:10; Rare:208 | ||||
| chr19:50383955-50384459 | Common:7; Rare:360; Clinvar:4; Clinvar (benign):7 | ||||
| chr19:50476358-50476659 | Rare:235 | ||||
| chr19:50476610-50477100 | Rare:359 | ||||
| chr19:50480570-50480940 | Common:4; Rare:134 | ||||
| chr19:50510858-50511616 | Common:14; Rare:529 | ||||
| chr19:50639710-50640070 | Common:15; Rare:244 | ||||
| chr19:50657995-50658666 | Common:3; Rare:422 |