| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50025304-50025743 | Common:7; Rare:148 | ||||
| chr19:50025872-50026151 | Common:1; Rare:74 | ||||
| chr19:50203516-50203697 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:50329613-50329843 | Rare:79 | ||||
| chr19:50333487-50333626 | Common:2; Rare:25 | ||||
| chr19:50333874-50333968 | Rare:50 | ||||
| chr19:50358424-50358774 | Common:1; Rare:145 | ||||
| chr19:50358795-50358921 | Common:1; Rare:25 | ||||
| chr19:50376232-50376599 | Common:7; Rare:93 | ||||
| chr19:50376654-50376987 | Common:5; Rare:86 | ||||
| chr19:50384016-50384467 | Common:6; Rare:180; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:50384580-50384706 | Rare:32 | ||||
| chr19:50476234-50476612 | Common:1; Rare:171 | ||||
| chr19:50511042-50511746 | Common:5; Rare:216 | ||||
| chr19:50568382-50568471 | Rare:7 |