| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49451754-49452002 | Common:3; Rare:64 | ||||
| chr19:49527806-49528024 | Common:4; Rare:70 | ||||
| chr19:49580540-49580670 | Rare:42 | ||||
| chr19:49665739-49666034 | Common:3; Rare:138; Clinvar (pathogenic):1 | ||||
| chr19:49867531-49867687 | Common:3; Rare:43 | ||||
| chr19:49877341-49877717 | Common:1; Rare:93 | ||||
| chr19:49929923-49930209 | Common:1; Rare:67 | ||||
| chr19:50333891-50333933 | Rare:14 | ||||
| chr19:50476213-50476544 | Common:1; Rare:154 | ||||
| chr19:51366335-51366551 | Common:5; Rare:57; Clinvar (benign):2 | ||||
| chr19:52008189-52008305 | Rare:32 | ||||
| chr19:52028336-52028462 | Common:3; Rare:26 | ||||
| chr19:52297033-52297198 | Common:18; Rare:42 | ||||
| chr19:52369844-52369954 | Common:1; Rare:34 | ||||
| chr19:52397733-52397890 | Common:4; Rare:48 |