| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50384022-50384381 | Common:2; Rare:153; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476247-50476556 | Rare:146 | ||||
| chr19:50511099-50511278 | Common:1; Rare:66 | ||||
| chr19:50804570-50804854 | Common:7; Rare:91 | ||||
| chr19:50870564-50870651 | Common:2; Rare:24 | ||||
| chr19:51108357-51108620 | Common:1; Rare:58 | ||||
| chr19:51366309-51366555 | Common:5; Rare:71; Clinvar (benign):2 | ||||
| chr19:51887863-51888054 | Rare:67 | ||||
| chr19:51927324-51927487 | Common:1; Rare:49 | ||||
| chr19:52008173-52008349 | Rare:49 | ||||
| chr19:52028327-52028471 | Common:3; Rare:34 | ||||
| chr19:52048652-52048687 | Rare:7 | ||||
| chr19:52269440-52269603 | Common:1; Rare:57 | ||||
| chr19:52296986-52297219 | Common:18; Rare:57 | ||||
| chr19:52369874-52369966 | Common:1; Rare:33 |