| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46986190-46986403 | Common:1; Rare:30 | ||||
| chr3:46998717-46999043 | Common:1; Rare:114; Clinvar:4 | ||||
| chr3:48590765-48590937 | Common:1; Rare:40 | ||||
| chr3:48592857-48593142 | Rare:88; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr3:49101429-49101640 | Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:50157272-50157414 | Rare:31 | ||||
| chr3:54636443-54636723 | Rare:76 | ||||
| chr3:54637730-54637791 | Rare:15 | ||||
| chr3:54637848-54638047 | Common:1; Rare:48 | ||||
| chr3:54639818-54640076 | Common:2; Rare:70 | ||||
| chr3:61560828-61561040 | Common:3; Rare:60 | ||||
| chr3:64684861-64685142 | Rare:55 | ||||
| chr3:75435090-75435388 | Common:4; Rare:97 | ||||
| chr3:101576984-101577041 | Rare:14 | ||||
| chr3:101676256-101676468 | Common:2; Rare:71 |