| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:31572870-31573027 | Rare:43 | ||||
| chr20:31604242-31604456 | Common:1; Rare:88 | ||||
| chr20:31712777-31712914 | Rare:13 | ||||
| chr20:32475293-32475612 | Common:1; Rare:74 | ||||
| chr20:35320459-35320603 | Common:1; Rare:17 | ||||
| chr20:35625915-35626162 | Rare:55 | ||||
| chr20:35871410-35871724 | Common:1; Rare:55 | ||||
| chr20:36050904-36051131 | Common:3; Rare:82 | ||||
| chr20:43843496-43843672 | Common:2; Rare:27 | ||||
| chr20:45424261-45424503 | Common:2; Rare:64; Clinvar (pathogenic):1 | ||||
| chr20:45780814-45780971 | Common:1; Rare:23 | ||||
| chr20:46770453-46770650 | Rare:31 | ||||
| chr20:47358876-47358940 | Rare:12 | ||||
| chr20:48897541-48897614 | Rare:12 | ||||
| chr20:50561646-50561837 | Common:2; Rare:28 |