Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:69560089-69560290 | Common:3; Rare:50 | ||||
chr5:71455536-71455690 | Rare:44 | ||||
chr5:71587135-71587409 | Common:1; Rare:95; Clinvar (benign):2 | ||||
chr5:72507288-72507621 | Common:1; Rare:64 | ||||
chr5:72816468-72816735 | Common:4; Rare:100 | ||||
chr5:72955849-72956091 | Common:1; Rare:111 | ||||
chr5:73498305-73498693 | Common:3; Rare:130 | ||||
chr5:73565420-73565826 | Common:7; Rare:129 | ||||
chr5:74640493-74640659 | Common:1; Rare:42 | ||||
chr5:74640723-74640987 | Common:2; Rare:83 | ||||
chr5:74685525-74685534 | Rare:1 | ||||
chr5:74767043-74767361 | Common:3; Rare:101 | ||||
chr5:75336966-75337290 | Common:3; Rare:110 | ||||
chr5:75511603-75511921 | Common:1; Rare:114 | ||||
chr5:76715844-76716158 | Common:6; Rare:89 |