| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58895279-58895427 | Common:1; Rare:31 | ||||
| chr20:58896879-58897124 | Common:2; Rare:62 | ||||
| chr20:58908169-58908566 | Common:2; Rare:73 | ||||
| chr20:58908853-58909423 | Common:5; Rare:133; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr20:58909945-58910683 | Common:2; Rare:169 | ||||
| chr20:58981124-58981336 | Common:2; Rare:100 | ||||
| chr20:59006971-59007073 | Rare:29 | ||||
| chr20:59032283-59032573 | Common:2; Rare:118; Clinvar (benign):3 | ||||
| chr20:59042728-59042975 | Common:1; Rare:85 | ||||
| chr20:59940276-59940489 | Rare:85 | ||||
| chr20:62143304-62143809 | Common:6; Rare:216 | ||||
| chr20:62302705-62303044 | Common:2; Rare:96 | ||||
| chr20:62308808-62309085 | Common:4; Rare:111 | ||||
| chr20:62386938-62387131 | Common:3; Rare:85 | ||||
| chr20:62937809-62938165 | Common:2; Rare:123 |