| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33993672-33994128 | Common:3; Rare:153 | ||||
| chr20:34112101-34112423 | Rare:104 | ||||
| chr20:34302971-34303393 | Common:1; Rare:164; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:34363113-34363349 | Rare:68 | ||||
| chr20:34516327-34516451 | Common:1; Rare:50 | ||||
| chr20:34677074-34677320 | Rare:64 | ||||
| chr20:34955733-34955817 | Common:1; Rare:33; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:35092706-35093002 | Common:2; Rare:125 | ||||
| chr20:35147109-35147437 | Common:1; Rare:118 | ||||
| chr20:35278093-35278227 | Common:3; Rare:52 | ||||
| chr20:35284480-35284955 | Common:4; Rare:133 | ||||
| chr20:35292320-35292592 | Common:2; Rare:67 | ||||
| chr20:35542374-35542552 | Rare:60 | ||||
| chr20:35556713-35557094 | Common:2; Rare:99 | ||||
| chr20:35664855-35664984 | Common:1; Rare:38 |