| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34303250-34303393 | Common:1; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:34516278-34516450 | Common:3; Rare:68 | ||||
| chr20:34677083-34677311 | Rare:56 | ||||
| chr20:35171878-35172110 | Rare:41 | ||||
| chr20:35284485-35284819 | Common:3; Rare:99 | ||||
| chr20:35455049-35455294 | Common:1; Rare:84 | ||||
| chr20:35542364-35542531 | Rare:58 | ||||
| chr20:35699185-35699260 | Rare:9 | ||||
| chr20:35699305-35699599 | Rare:84; Clinvar (benign):3 | ||||
| chr20:35742158-35742617 | Common:5; Rare:138 | ||||
| chr20:36236436-36236491 | Rare:9 | ||||
| chr20:36746059-36746297 | Common:2; Rare:85 | ||||
| chr20:37095946-37096032 | Rare:37 | ||||
| chr20:37178861-37179205 | Rare:103 | ||||
| chr20:37289605-37289669 | Common:1; Rare:20 |