| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25310246-25310538 | Rare:64 | ||||
| chr20:25390817-25391046 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:25407542-25407905 | Common:2; Rare:141; Clinvar (pathogenic):1 | ||||
| chr20:25407913-25407959 | Common:1; Rare:23 | ||||
| chr20:25623861-25624053 | Common:1; Rare:93 | ||||
| chr20:25624055-25624203 | Rare:53 | ||||
| chr20:25696772-25697085 | Common:3; Rare:87 | ||||
| chr20:31514626-31514731 | Rare:29 | ||||
| chr20:31605124-31605488 | Common:9; Rare:196 | ||||
| chr20:31722402-31722687 | Common:1; Rare:58 | ||||
| chr20:31722720-31722937 | Rare:55 | ||||
| chr20:31723513-31723790 | Common:2; Rare:91 | ||||
| chr20:31739130-31739612 | Common:3; Rare:102 | ||||
| chr20:31845562-31845851 | Rare:57 | ||||
| chr20:32109668-32109765 | Rare:47 |