| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:57481552-57481647 | Common:1; Rare:18 | ||||
| chr20:57481663-57481702 | Common:2; Rare:7 | ||||
| chr20:57619165-57619275 | Common:1; Rare:23 | ||||
| chr20:57619285-57619678 | Common:4; Rare:80 | ||||
| chr20:57628578-57628600 | Rare:6 | ||||
| chr20:57680276-57680425 | Common:2; Rare:24 | ||||
| chr20:57681136-57681415 | Rare:53 | ||||
| chr20:57682782-57682980 | Common:1; Rare:46 | ||||
| chr20:58236714-58236831 | Rare:25 | ||||
| chr20:58237138-58237303 | Rare:39 | ||||
| chr20:58306869-58307050 | Common:1; Rare:32 | ||||
| chr20:58310543-58310591 | Rare:6 | ||||
| chr20:58402990-58403057 | Common:2; Rare:19 | ||||
| chr20:58450340-58450487 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:58650189-58650270 | Common:1; Rare:27 |