| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49903845-49904008 | Common:1; Rare:51 | ||||
| chr3:49929740-49929913 | Rare:67 | ||||
| chr3:50267405-50267675 | Common:2; Rare:83 | ||||
| chr3:50268863-50269249 | Common:1; Rare:88 | ||||
| chr3:50299329-50299692 | Common:1; Rare:90 | ||||
| chr3:50303570-50303795 | Common:2; Rare:38 | ||||
| chr3:50328163-50328362 | Rare:60 | ||||
| chr3:50350697-50350902 | Common:1; Rare:31 | ||||
| chr3:50359344-50359606 | Common:3; Rare:69 | ||||
| chr3:50365106-50365382 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:50567702-50567866 | Rare:52 | ||||
| chr3:50569425-50569574 | Common:1; Rare:37 | ||||
| chr3:50611737-50611908 | Rare:39 | ||||
| chr3:50616934-50617203 | Common:7; Rare:50 | ||||
| chr3:50617290-50617559 | Common:1; Rare:50 |