| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:21303029-21303468 | Rare:134 | ||||
| chr20:21303734-21303855 | Rare:36 | ||||
| chr20:25247949-25248108 | Common:1; Rare:59 | ||||
| chr20:25390813-25391005 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:25623913-25624148 | Common:1; Rare:91 | ||||
| chr20:25696766-25696939 | Common:3; Rare:57 | ||||
| chr20:31722731-31722956 | Rare:55 | ||||
| chr20:31739093-31739402 | Common:2; Rare:85 | ||||
| chr20:32207683-32207934 | Common:3; Rare:93 | ||||
| chr20:33401481-33401589 | Rare:29 | ||||
| chr20:33993080-33993258 | Rare:49 | ||||
| chr20:33993503-33993967 | Common:3; Rare:143 | ||||
| chr20:34516278-34516446 | Common:3; Rare:63 | ||||
| chr20:34558533-34558796 | Common:1; Rare:72 | ||||
| chr20:34704159-34704354 | Common:1; Rare:65 |