| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3796124-3796531 | Common:8; Rare:157 | ||||
| chr20:3820060-3820349 | Common:4; Rare:114 | ||||
| chr20:3820427-3820617 | Common:1; Rare:110 | ||||
| chr20:3846703-3846899 | Common:1; Rare:109 | ||||
| chr20:3888547-3888929 | Common:2; Rare:162 | ||||
| chr20:3889021-3889469 | Common:6; Rare:454; Clinvar:18; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr20:3889490-3889877 | Common:11; Rare:226; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr20:4015516-4015704 | Common:3; Rare:72 | ||||
| chr20:4148537-4148925 | Rare:179 | ||||
| chr20:4171580-4172480 | Common:3; Rare:156 | ||||
| chr20:4686216-4686511 | Common:2; Rare:124; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:5112836-5113194 | Common:3; Rare:241 | ||||
| chr20:5119230-5119630 | Common:6; Rare:243 | ||||
| chr20:5119884-5120198 | Common:2; Rare:204 | ||||
| chr20:5126521-5127090 | Common:8; Rare:340 |