Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:72816524-72816793 | Common:4; Rare:102 | ||||
chr5:72955854-72956091 | Common:1; Rare:107 | ||||
chr5:73498305-73498698 | Common:3; Rare:132 | ||||
chr5:73565420-73565826 | Common:7; Rare:129 | ||||
chr5:74767043-74767361 | Common:3; Rare:101 | ||||
chr5:75511591-75511921 | Common:1; Rare:116 | ||||
chr5:75717364-75717663 | Common:5; Rare:75 | ||||
chr5:77087201-77087345 | Rare:33 | ||||
chr5:78360355-78360684 | Common:5; Rare:129 | ||||
chr5:79069627-79069777 | Rare:52; Clinvar (benign):2 | ||||
chr5:79513087-79513286 | Common:1; Rare:41 | ||||
chr5:79689772-79690056 | Common:3; Rare:90 | ||||
chr5:79991231-79991347 | Rare:36 | ||||
chr5:80256035-80256235 | Common:1; Rare:80 | ||||
chr5:80407856-80408096 | Common:1; Rare:88 |