| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3846600-3846938 | Common:4; Rare:86 | ||||
| chr20:3847194-3847247 | Rare:8 | ||||
| chr20:3847249-3847318 | Rare:18 | ||||
| chr20:3888775-3888867 | Rare:22 | ||||
| chr20:3888874-3889466 | Common:3; Rare:289; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr20:3889659-3889905 | Common:6; Rare:106; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:4015472-4015785 | Common:4; Rare:112 | ||||
| chr20:4686212-4686339 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr20:4686359-4686495 | Rare:25 | ||||
| chr20:4814628-4815272 | Common:13; Rare:164 | ||||
| chr20:4823403-4823847 | Common:5; Rare:100 | ||||
| chr20:5001420-5001624 | Common:1; Rare:59 | ||||
| chr20:5112966-5113302 | Rare:118 | ||||
| chr20:5119231-5119659 | Common:3; Rare:133 | ||||
| chr20:5119752-5120441 | Common:2; Rare:200 |