| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25195462-25195979 | Common:9; Rare:148 | ||||
| chr20:25247897-25248414 | Common:2; Rare:206 | ||||
| chr20:25389688-25389793 | Rare:27 | ||||
| chr20:25389865-25389924 | Rare:18 | ||||
| chr20:25390375-25390635 | Common:11; Rare:116 | ||||
| chr20:25390689-25391190 | Common:5; Rare:178; Clinvar:4; Clinvar (benign):3 | ||||
| chr20:25407421-25407841 | Common:6; Rare:146; Clinvar (pathogenic):1 | ||||
| chr20:25407871-25407893 | Rare:12 | ||||
| chr20:25407905-25407971 | Common:2; Rare:28 | ||||
| chr20:25623638-25624605 | Common:6; Rare:313 | ||||
| chr20:25696476-25697105 | Common:4; Rare:197 | ||||
| chr20:31514367-31514599 | Common:6; Rare:106 | ||||
| chr20:31547096-31547516 | Common:1; Rare:97 | ||||
| chr20:31605112-31605320 | Common:7; Rare:91 | ||||
| chr20:31722426-31723034 | Common:1; Rare:129 |