| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52287724-52287874 | Common:4; Rare:105 | ||||
| chr3:52287960-52288150 | Rare:105 | ||||
| chr3:52289779-52290145 | Rare:97 | ||||
| chr3:52409867-52410070 | Rare:111; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:52410315-52410680 | Rare:133 | ||||
| chr3:52455409-52455642 | Common:4; Rare:140 | ||||
| chr3:52533721-52534056 | Common:12; Rare:194 | ||||
| chr3:52534957-52535062 | Common:1; Rare:23 | ||||
| chr3:52685533-52685723 | Rare:104 | ||||
| chr3:52685849-52686214 | Common:4; Rare:276 | ||||
| chr3:52704543-52705187 | Rare:175 | ||||
| chr3:52705533-52706223 | Common:8; Rare:416 | ||||
| chr3:52770887-52771092 | Common:7; Rare:116 | ||||
| chr3:52897501-52897757 | Rare:93 | ||||
| chr3:53045267-53045750 | Common:7; Rare:325 |