| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58515291-58515613 | Common:4; Rare:56 | ||||
| chr20:58651368-58651429 | Rare:11 | ||||
| chr20:58651563-58651756 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:58888808-58889005 | Common:1; Rare:58 | ||||
| chr20:58891602-58892190 | Common:9; Rare:263; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:58894492-58894788 | Rare:65 | ||||
| chr20:58895008-58895159 | Rare:34 | ||||
| chr20:58896815-58897123 | Common:2; Rare:80 | ||||
| chr20:58897132-58897263 | Rare:35 | ||||
| chr20:58909117-58909230 | Common:1; Rare:39; Clinvar:2 | ||||
| chr20:58981160-58981349 | Common:2; Rare:90 | ||||
| chr20:59032224-59032241 | Rare:6 | ||||
| chr20:59940297-59940501 | Rare:82 | ||||
| chr20:62143297-62143812 | Common:6; Rare:220 | ||||
| chr20:62182954-62183057 | Rare:28 |