Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:30257675-30257823 | Rare:40 | ||||
chr22:30969061-30969283 | Common:2; Rare:63 | ||||
chr22:38336179-38336278 | Rare:25 | ||||
chr22:46069842-46070057 | Rare:45 | ||||
chr3:40453175-40453466 | Common:4; Rare:65 | ||||
chr3:75435123-75435308 | Common:2; Rare:60 | ||||
chr3:98536583-98536792 | Rare:40 | ||||
chr3:98981116-98981364 | Common:2; Rare:35 | ||||
chr3:101576981-101577049 | Rare:16 | ||||
chr3:101940568-101940899 | Common:2; Rare:54 | ||||
chr3:112409116-112409242 | Rare:22 | ||||
chr3:129794512-129794673 | Rare:26 | ||||
chr3:131361604-131361916 | Common:3; Rare:93 | ||||
chr3:169765053-169765238 | Rare:74; Clinvar (pathogenic):2 | ||||
chr4:52712223-52712518 | Common:4; Rare:75 |