| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46364366-46364531 | Rare:62 | ||||
| chr20:47318997-47319137 | Common:1; Rare:44 | ||||
| chr20:47501761-47501987 | Common:1; Rare:78 | ||||
| chr20:49046207-49046346 | Common:3; Rare:41 | ||||
| chr20:49915462-49915632 | Common:3; Rare:63 | ||||
| chr20:50958471-50958845 | Common:1; Rare:131; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:56392174-56392545 | Common:3; Rare:102 | ||||
| chr20:57709946-57710192 | Rare:68 | ||||
| chr20:58309414-58309715 | Common:2; Rare:118 | ||||
| chr20:58909166-58909423 | Common:3; Rare:58; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr20:58910375-58910717 | Common:2; Rare:73 | ||||
| chr20:59006989-59007136 | Rare:47 | ||||
| chr20:62143318-62143803 | Common:6; Rare:201 | ||||
| chr20:62182954-62183049 | Rare:23 | ||||
| chr20:62386908-62387132 | Common:3; Rare:101 |