| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915732-46916082 | Common:3; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176435-47176624 | Common:1; Rare:125; Clinvar (benign):5 | ||||
| chr2:53786870-53787179 | Common:1; Rare:116 | ||||
| chr2:55232316-55232736 | Common:2; Rare:120 | ||||
| chr2:55519550-55519751 | Common:1; Rare:55 | ||||
| chr2:61017440-61017769 | Common:1; Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144926-61145082 | Common:1; Rare:48 | ||||
| chr2:61888548-61888692 | Common:1; Rare:61 | ||||
| chr2:64988316-64988508 | Common:1; Rare:37 | ||||
| chr2:65227597-65227852 | Rare:65 | ||||
| chr2:68157522-68157896 | Common:2; Rare:188 | ||||
| chr2:70087374-70087876 | Common:2; Rare:179 | ||||
| chr2:71130220-71130345 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:74198440-74198620 | Rare:68 | ||||
| chr2:74421618-74421770 | Rare:49 |