Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:123008705-123009011 | Common:6; Rare:79; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124461733-124461851 | Common:4; Rare:43 | ||||
chr10:124791829-124791959 | Rare:61 | ||||
chr10:125719494-125719727 | Rare:73 | ||||
chr10:125823200-125823561 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
chr10:132331847-132332122 | Common:10; Rare:76 | ||||
chr10:133308835-133308989 | Rare:72 | ||||
chr11:207361-207511 | Common:4; Rare:60 | ||||
chr11:208617-208843 | Rare:79 | ||||
chr11:576412-576506 | Rare:33 | ||||
chr11:777463-777617 | Common:1; Rare:68 | ||||
chr11:842471-842895 | Common:7; Rare:175 | ||||
chr11:2992252-2992516 | Common:2; Rare:102 | ||||
chr11:3797494-3797840 | Rare:121 | ||||
chr11:4094736-4094832 | Common:1; Rare:28 |