| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3767714-3767928 | Common:2; Rare:66 | ||||
| chr20:3820469-3820582 | Rare:44 | ||||
| chr20:3846724-3846891 | Rare:50 | ||||
| chr20:3888657-3888868 | Common:1; Rare:52 | ||||
| chr20:3889158-3889401 | Common:1; Rare:125; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:4148678-4148867 | Rare:61 | ||||
| chr20:4823381-4823704 | Common:4; Rare:67 | ||||
| chr20:4823736-4823796 | Rare:16 | ||||
| chr20:5001443-5001669 | Common:1; Rare:62 | ||||
| chr20:5112852-5113178 | Common:1; Rare:118 | ||||
| chr20:5119907-5120149 | Common:1; Rare:84 | ||||
| chr20:5126534-5126814 | Common:3; Rare:79 | ||||
| chr20:5610924-5611154 | Common:2; Rare:81 | ||||
| chr20:5750290-5750461 | Rare:43 | ||||
| chr20:5911266-5911681 | Common:3; Rare:120 |