Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:73565380-73565890 | Common:7; Rare:151 | ||||
chr5:73813224-73813598 | Common:1; Rare:75 | ||||
chr5:74640487-74640667 | Common:1; Rare:47 | ||||
chr5:74640723-74640934 | Common:1; Rare:66 | ||||
chr5:74767038-74767357 | Common:3; Rare:100 | ||||
chr5:75336891-75337292 | Common:3; Rare:136 | ||||
chr5:75511610-75511913 | Common:1; Rare:112 | ||||
chr5:75717364-75717666 | Common:5; Rare:77 | ||||
chr5:76715844-76716153 | Common:5; Rare:88 | ||||
chr5:77030292-77030425 | Rare:46 | ||||
chr5:77086636-77086736 | Rare:27 | ||||
chr5:77087294-77087464 | Rare:19 | ||||
chr5:78294609-78294863 | Common:1; Rare:98; Clinvar:1 | ||||
chr5:78360355-78360684 | Common:5; Rare:129 | ||||
chr5:79069627-79069770 | Rare:51; Clinvar (benign):2 |