Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31605130-31605334 | Common:7; Rare:91 | ||||
chr20:32207724-32207904 | Common:1; Rare:63 | ||||
chr20:32743340-32743631 | Common:1; Rare:71 | ||||
chr20:34516218-34516438 | Common:3; Rare:73 | ||||
chr20:35699344-35699429 | Rare:23 | ||||
chr20:36605527-36605831 | Common:2; Rare:115 | ||||
chr20:38805605-38805760 | Common:2; Rare:35 | ||||
chr20:44210691-44211009 | Common:4; Rare:114 | ||||
chr20:45857339-45857674 | Common:3; Rare:94 | ||||
chr20:45891262-45891400 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
chr20:45910920-45911146 | Common:4; Rare:58 | ||||
chr20:47356672-47356876 | Rare:46 | ||||
chr20:49046204-49046357 | Common:3; Rare:46 | ||||
chr20:49219205-49219446 | Common:1; Rare:106 | ||||
chr20:49915461-49915636 | Common:3; Rare:63 |