Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:129974572-129974721 | Rare:34 | ||||
chr3:130746763-130746934 | Common:3; Rare:52 | ||||
chr3:130893938-130894289 | Common:3; Rare:105 | ||||
chr3:130894455-130894622 | Common:1; Rare:35; Clinvar (benign):1 | ||||
chr3:131026723-131026879 | Common:2; Rare:37 | ||||
chr3:131381479-131381811 | Common:2; Rare:84 | ||||
chr3:131502775-131502863 | Rare:35 | ||||
chr3:131502865-131503016 | Common:1; Rare:63 | ||||
chr3:132417177-132417702 | Common:6; Rare:174 | ||||
chr3:132659799-132659989 | Common:3; Rare:41 | ||||
chr3:133038156-133038424 | Common:1; Rare:91 | ||||
chr3:133573815-133574032 | Rare:75 | ||||
chr3:133661780-133662069 | Rare:71 | ||||
chr3:133895473-133895866 | Common:3; Rare:129 | ||||
chr3:134373777-134373827 | Rare:18 |