| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3801766-3801999 | Common:1; Rare:67 | ||||
| chr20:3820504-3820858 | Common:1; Rare:114 | ||||
| chr20:3846724-3846893 | Rare:50 | ||||
| chr20:3889155-3889362 | Rare:102; Clinvar:3 | ||||
| chr20:3889576-3889874 | Common:6; Rare:136; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr20:4686331-4686508 | Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:4740425-4740569 | Common:3; Rare:29 | ||||
| chr20:4823385-4823709 | Common:4; Rare:64 | ||||
| chr20:5001443-5001686 | Common:1; Rare:66 | ||||
| chr20:5112846-5113171 | Common:1; Rare:119 | ||||
| chr20:5119441-5119580 | Common:2; Rare:62 | ||||
| chr20:5119907-5120095 | Common:1; Rare:66 | ||||
| chr20:5126144-5126282 | Common:1; Rare:23 | ||||
| chr20:5126555-5127095 | Common:4; Rare:171 | ||||
| chr20:5548354-5548518 | Rare:30 |