| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:23049654-23049729 | Common:3; Rare:24 | ||||
| chr20:23086314-23086461 | Rare:27 | ||||
| chr20:23350522-23350869 | Common:2; Rare:107 | ||||
| chr20:24992698-24992827 | Common:3; Rare:59 | ||||
| chr20:25195596-25195769 | Common:2; Rare:59 | ||||
| chr20:25623952-25624133 | Common:1; Rare:60 | ||||
| chr20:25696766-25696928 | Common:1; Rare:53 | ||||
| chr20:31547305-31547431 | Rare:28 | ||||
| chr20:31605740-31605787 | Rare:26 | ||||
| chr20:31739107-31739357 | Common:1; Rare:63 | ||||
| chr20:32207676-32207939 | Common:3; Rare:97 | ||||
| chr20:33401488-33401589 | Rare:26 | ||||
| chr20:33993796-33994125 | Common:1; Rare:121 | ||||
| chr20:34112117-34112426 | Rare:103 | ||||
| chr20:34303266-34303357 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 |