| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:20712404-20712585 | Rare:46 | ||||
| chr20:21125852-21126175 | Common:3; Rare:118; Clinvar (pathogenic):1 | ||||
| chr20:21303252-21303471 | Rare:72 | ||||
| chr20:22584257-22584480 | Common:1; Rare:67 | ||||
| chr20:23049243-23049357 | Rare:41; Clinvar:1 | ||||
| chr20:23049651-23049857 | Common:3; Rare:71; Clinvar (pathogenic):1 | ||||
| chr20:23086265-23086509 | Rare:53 | ||||
| chr20:23350489-23350886 | Common:4; Rare:121 | ||||
| chr20:23361807-23362226 | Common:5; Rare:147 | ||||
| chr20:24992698-24992839 | Common:4; Rare:66 | ||||
| chr20:25058377-25058429 | Common:1; Rare:10 | ||||
| chr20:25195588-25195903 | Common:5; Rare:97 | ||||
| chr20:25247739-25248189 | Common:2; Rare:152 | ||||
| chr20:25290339-25290621 | Common:3; Rare:99 | ||||
| chr20:25623952-25624194 | Common:1; Rare:86 |