| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50333814-50333940 | Common:2; Rare:51 | ||||
| chr19:50358831-50358930 | Common:1; Rare:17 | ||||
| chr19:50365603-50365804 | Common:1; Rare:44 | ||||
| chr19:50376207-50376556 | Common:6; Rare:87 | ||||
| chr19:50384017-50384442 | Common:5; Rare:169; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:50415773-50415829 | Rare:15; Clinvar:10; Clinvar (benign):4 | ||||
| chr19:50415837-50415929 | Rare:24 | ||||
| chr19:50418238-50418542 | Common:3; Rare:86 | ||||
| chr19:50418784-50419030 | Rare:89 | ||||
| chr19:50476423-50476603 | Rare:74 | ||||
| chr19:50511076-50511596 | Common:5; Rare:168 | ||||
| chr19:50803611-50803895 | Common:2; Rare:83 | ||||
| chr19:50804006-50804316 | Common:5; Rare:98 | ||||
| chr19:50804567-50804916 | Common:8; Rare:110 | ||||
| chr19:50820303-50820378 | Rare:25 |