Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:9397436-9397902 | Common:1; Rare:145 | ||||
chr3:9792414-9792570 | Rare:40 | ||||
chr3:9792711-9793123 | Common:3; Rare:146 | ||||
chr3:9917033-9917158 | Common:1; Rare:26 | ||||
chr3:9933517-9933863 | Common:2; Rare:142; Clinvar:3 | ||||
chr3:10026329-10026446 | Rare:36 | ||||
chr3:10115524-10115713 | Common:3; Rare:69 | ||||
chr3:11643875-11643973 | Rare:35 | ||||
chr3:11720705-11720813 | Rare:16 | ||||
chr3:12158858-12158952 | Rare:30 | ||||
chr3:12287775-12287930 | Common:5; Rare:25 | ||||
chr3:12484334-12484554 | Common:5; Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
chr3:12545525-12545824 | Common:3; Rare:61 | ||||
chr3:12664071-12664300 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
chr3:13479972-13480342 | Common:3; Rare:92 |