| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18507425-18507624 | Rare:52; Clinvar:1 | ||||
| chr20:18507781-18507957 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:18567295-18567543 | Common:3; Rare:91 | ||||
| chr20:20017238-20017396 | Rare:57 | ||||
| chr20:20712456-20712729 | Common:2; Rare:87 | ||||
| chr20:21125836-21126175 | Common:3; Rare:124; Clinvar (pathogenic):1 | ||||
| chr20:21303126-21303471 | Rare:111 | ||||
| chr20:21303556-21303860 | Common:1; Rare:88 | ||||
| chr20:23350483-23350869 | Common:4; Rare:120 | ||||
| chr20:23361853-23362229 | Common:3; Rare:128 | ||||
| chr20:23421400-23421645 | Common:4; Rare:106 | ||||
| chr20:24992678-24992920 | Common:7; Rare:110 | ||||
| chr20:25195595-25195784 | Common:2; Rare:65 | ||||
| chr20:25407556-25407778 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
| chr20:25585477-25585696 | Common:3; Rare:67 |