| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3758653-3758821 | Rare:38 | ||||
| chr20:3767698-3768056 | Common:4; Rare:114 | ||||
| chr20:3795720-3795849 | Common:1; Rare:31 | ||||
| chr20:3846724-3846894 | Rare:50 | ||||
| chr20:3888832-3888946 | Rare:27 | ||||
| chr20:3889072-3889396 | Common:2; Rare:179; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr20:4015491-4015723 | Common:4; Rare:79 | ||||
| chr20:4148728-4148890 | Rare:49 | ||||
| chr20:4815141-4815212 | Common:1; Rare:19 | ||||
| chr20:4823385-4823703 | Common:4; Rare:63 | ||||
| chr20:4823736-4823913 | Rare:43 | ||||
| chr20:5112858-5113181 | Common:1; Rare:119 | ||||
| chr20:5119859-5120172 | Common:1; Rare:106 | ||||
| chr20:5126538-5126780 | Common:3; Rare:67 | ||||
| chr20:5610351-5610516 | Common:3; Rare:30 |