| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:13008911-13009344 | Common:2; Rare:100 | ||||
| chr20:13784871-13785112 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13995246-13995617 | Rare:106 | ||||
| chr20:16573278-16573573 | Common:1; Rare:87 | ||||
| chr20:16729878-16730073 | Rare:61 | ||||
| chr20:17226827-17227092 | Common:2; Rare:75 | ||||
| chr20:17228043-17228198 | Common:2; Rare:26 | ||||
| chr20:17569157-17569244 | Rare:20 | ||||
| chr20:17569963-17570218 | Common:3; Rare:111 | ||||
| chr20:17682026-17682624 | Common:6; Rare:184 | ||||
| chr20:17693534-17693696 | Common:1; Rare:35 | ||||
| chr20:17968375-17968633 | Common:5; Rare:109 | ||||
| chr20:17968783-17969170 | Common:3; Rare:131 | ||||
| chr20:17969515-17969581 | Rare:11 | ||||
| chr20:17969652-17970000 | Common:3; Rare:100; Clinvar (benign):3 |