Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:79236012-79236125 | Common:1; Rare:45 | ||||
chr5:79514533-79514674 | Rare:37 | ||||
chr5:79991178-79991354 | Rare:56 | ||||
chr5:80407805-80408104 | Common:1; Rare:111 | ||||
chr5:80487937-80488118 | Common:1; Rare:60 | ||||
chr5:80654548-80654724 | Common:5; Rare:111 | ||||
chr5:81301485-81301685 | Common:4; Rare:67 | ||||
chr5:81971752-81972059 | Common:3; Rare:118 | ||||
chr5:82278319-82278692 | Common:4; Rare:121 | ||||
chr5:83077334-83077615 | Common:1; Rare:83 | ||||
chr5:83471869-83471889 | Rare:3 | ||||
chr5:84384378-84384529 | Rare:44 | ||||
chr5:84384589-84384731 | Rare:70 | ||||
chr5:87267733-87268015 | Common:4; Rare:92 | ||||
chr5:87268193-87268269 | Common:1; Rare:17; Clinvar (benign):1 |