| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:298255-298577 | Common:1; Rare:96 | ||||
| chr20:300110-300291 | Common:2; Rare:35 | ||||
| chr20:309986-310153 | Common:4; Rare:28 | ||||
| chr20:326377-326458 | Rare:29 | ||||
| chr20:327081-327928 | Common:10; Rare:244 | ||||
| chr20:328380-328704 | Common:10; Rare:65 | ||||
| chr20:341402-341594 | Common:1; Rare:29 | ||||
| chr20:419818-420008 | Common:9; Rare:40 | ||||
| chr20:420043-420401 | Common:2; Rare:66 | ||||
| chr20:421046-421306 | Common:2; Rare:80 | ||||
| chr20:427092-427491 | Rare:78; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr20:444633-444817 | Common:1; Rare:34 | ||||
| chr20:489976-490239 | Common:1; Rare:50 | ||||
| chr20:582251-582354 | Rare:19 | ||||
| chr20:1141350-1141477 | Common:1; Rare:22 |