Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:101576954-101577082 | Common:1; Rare:35 | ||||
chr3:101676277-101676474 | Common:1; Rare:65 | ||||
chr3:107240586-107240751 | Rare:72 | ||||
chr3:112639775-112640030 | Common:1; Rare:65 | ||||
chr3:112640343-112640431 | Common:1; Rare:11 | ||||
chr3:123739712-123739883 | Common:1; Rare:28 | ||||
chr3:131361661-131361916 | Common:2; Rare:73 | ||||
chr3:134312332-134312358 | Rare:6 | ||||
chr3:150408860-150408998 | Rare:39 | ||||
chr3:157174836-157175129 | Common:3; Rare:125 | ||||
chr3:169765029-169765209 | Rare:79; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr3:177441780-177442015 | Common:1; Rare:32 | ||||
chr3:177934294-177934605 | Common:1; Rare:72 | ||||
chr3:183447517-183447680 | Common:1; Rare:42 | ||||
chr3:185658582-185658870 | Common:1; Rare:61 |