| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3796150-3796479 | Common:2; Rare:77 | ||||
| chr20:3846712-3846906 | Common:1; Rare:54 | ||||
| chr20:3888677-3888929 | Common:1; Rare:64 | ||||
| chr20:3889154-3889440 | Common:2; Rare:158; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr20:3889708-3889874 | Common:6; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:4148704-4148880 | Rare:59 | ||||
| chr20:4686302-4686523 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:5113027-5113161 | Rare:59 | ||||
| chr20:5119311-5119602 | Common:3; Rare:103 | ||||
| chr20:5119802-5120202 | Common:1; Rare:140 | ||||
| chr20:5126559-5127104 | Common:4; Rare:171 | ||||
| chr20:5610908-5611159 | Common:2; Rare:89 | ||||
| chr20:5750285-5750461 | Rare:45 | ||||
| chr20:5911347-5911590 | Common:2; Rare:70 | ||||
| chr20:5950275-5950744 | Common:8; Rare:143 |