| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50321282-50322100 | Common:3; Rare:238 | ||||
| chr3:50328103-50328400 | Common:3; Rare:222 | ||||
| chr3:50345227-50345846 | Rare:241; Clinvar (pathogenic):2 | ||||
| chr3:50350682-50350958 | Common:4; Rare:125 | ||||
| chr3:50350990-50351340 | Common:6; Rare:116 | ||||
| chr3:50359447-50359661 | Common:4; Rare:97 | ||||
| chr3:50365173-50365426 | Common:3; Rare:277; Clinvar:6; Clinvar (benign):3 | ||||
| chr3:50503580-50503816 | Common:3; Rare:152 | ||||
| chr3:50569025-50569659 | Common:6; Rare:312 | ||||
| chr3:50610691-50611606 | Common:4; Rare:216 | ||||
| chr3:50611569-50611913 | Common:1; Rare:189 | ||||
| chr3:50611936-50612344 | Common:4; Rare:217; Clinvar:3 | ||||
| chr3:50616813-50617292 | Common:22; Rare:190 | ||||
| chr3:50617384-50617548 | Common:1; Rare:43 | ||||
| chr3:50674501-50675087 | Common:4; Rare:255 |