| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31723446-31723838 | Common:3; Rare:125 | ||||
| chr20:31723909-31723985 | Rare:15 | ||||
| chr20:31738841-31738922 | Rare:10 | ||||
| chr20:31739006-31739404 | Common:4; Rare:100 | ||||
| chr20:31870427-31870637 | Common:1; Rare:63 | ||||
| chr20:31879620-31879775 | Rare:44 | ||||
| chr20:31880002-31880255 | Common:2; Rare:73 | ||||
| chr20:31951899-31952171 | Common:1; Rare:117 | ||||
| chr20:32109395-32109832 | Common:2; Rare:132 | ||||
| chr20:32109906-32110055 | Rare:34 | ||||
| chr20:32207656-32208017 | Common:4; Rare:131 | ||||
| chr20:32277459-32277694 | Rare:58 | ||||
| chr20:32357648-32358483 | Common:5; Rare:215; Clinvar:1 | ||||
| chr20:32358485-32358644 | Common:1; Rare:53; Clinvar:6; Clinvar (benign):1 | ||||
| chr20:32358815-32359032 | Common:3; Rare:84 |