| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3796124-3796565 | Common:4; Rare:99 | ||||
| chr20:3801011-3801386 | Common:1; Rare:106 | ||||
| chr20:3820484-3820612 | Rare:48 | ||||
| chr20:3846727-3846906 | Common:1; Rare:51 | ||||
| chr20:3888592-3888868 | Common:1; Rare:64 | ||||
| chr20:3889016-3889427 | Common:2; Rare:224; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr20:4015499-4015783 | Common:4; Rare:104 | ||||
| chr20:4148540-4148954 | Rare:104 | ||||
| chr20:4686209-4686511 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:4823434-4823572 | Common:3; Rare:30 | ||||
| chr20:5112721-5112796 | Rare:20 | ||||
| chr20:5119500-5119653 | Common:2; Rare:67 | ||||
| chr20:5119810-5120179 | Common:1; Rare:124 | ||||
| chr20:5126522-5127152 | Common:4; Rare:194 | ||||
| chr20:5610904-5611128 | Common:2; Rare:75 |