Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:69492340-69492649 | Common:2; Rare:72; Clinvar (benign):1 | ||||
chr5:69492698-69492875 | Rare:52 | ||||
chr5:71455573-71455694 | Rare:34 | ||||
chr5:71587202-71587408 | Common:1; Rare:62; Clinvar (benign):2 | ||||
chr5:72816500-72816696 | Common:3; Rare:68 | ||||
chr5:72955834-72956085 | Common:1; Rare:113 | ||||
chr5:73498359-73498563 | Common:1; Rare:62 | ||||
chr5:73565380-73565775 | Common:6; Rare:107 | ||||
chr5:74640494-74640667 | Common:1; Rare:47 | ||||
chr5:74640716-74640953 | Common:2; Rare:75 | ||||
chr5:74767110-74767294 | Common:1; Rare:56 | ||||
chr5:75336919-75337264 | Common:3; Rare:115 | ||||
chr5:75511610-75511914 | Common:1; Rare:112 | ||||
chr5:75717385-75717663 | Common:5; Rare:69 | ||||
chr5:77030284-77030407 | Rare:38 |