| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50582777-50583121 | Common:7; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628083-50628252 | Common:8; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50782423-50782520 | Rare:18 | ||||
| chr22:50783592-50783859 | Common:2; Rare:87 | ||||
| chr3:196739-197009 | Common:2; Rare:82 | ||||
| chr3:197202-197296 | Rare:32 | ||||
| chr3:3126775-3126990 | Common:4; Rare:94; Clinvar (benign):2 | ||||
| chr3:4303252-4303502 | Common:2; Rare:98 | ||||
| chr3:4493177-4493370 | Rare:72; Clinvar:1 | ||||
| chr3:5187327-5187663 | Common:5; Rare:133 | ||||
| chr3:8501641-8501937 | Common:2; Rare:110 | ||||
| chr3:9249552-9249742 | Common:1; Rare:42 | ||||
| chr3:9362978-9363098 | Common:1; Rare:45 | ||||
| chr3:9382984-9383210 | Rare:61 | ||||
| chr3:9397434-9397706 | Common:1; Rare:100 |