| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49690980-49691144 | Common:1; Rare:37 | ||||
| chr19:49877319-49877720 | Common:1; Rare:100 | ||||
| chr19:49929430-49929820 | Common:7; Rare:132 | ||||
| chr19:49929923-49930234 | Common:1; Rare:74 | ||||
| chr19:50384239-50384360 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr19:50476238-50476558 | Rare:148 | ||||
| chr19:50804590-50804892 | Common:5; Rare:89 | ||||
| chr19:51311571-51311866 | Common:4; Rare:56 | ||||
| chr19:51366335-51366505 | Common:5; Rare:46; Clinvar (benign):2 | ||||
| chr19:51887868-51888038 | Rare:59 | ||||
| chr19:51904933-51905146 | Common:3; Rare:67 | ||||
| chr19:51986782-51987025 | Common:1; Rare:67 | ||||
| chr19:52008132-52008303 | Rare:53 | ||||
| chr19:52028325-52028475 | Common:3; Rare:36 | ||||
| chr19:52139875-52140126 | Common:2; Rare:66 |