Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124791823-124792005 | Common:1; Rare:89 | ||||
chr10:125719464-125719727 | Rare:84 | ||||
chr10:125823200-125823568 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896302-125896599 | Common:2; Rare:17 | ||||
chr10:126905302-126905464 | Rare:62 | ||||
chr10:132331821-132332164 | Common:13; Rare:105 | ||||
chr10:133308835-133308974 | Rare:66 | ||||
chr11:207343-207725 | Common:8; Rare:130 | ||||
chr11:208654-208855 | Rare:77 | ||||
chr11:236324-236559 | Common:8; Rare:81 | ||||
chr11:236716-237032 | Common:4; Rare:95 | ||||
chr11:307579-307792 | Common:6; Rare:61 | ||||
chr11:308084-308435 | Common:8; Rare:121 | ||||
chr11:320533-320932 | Common:5; Rare:154; Clinvar:1 | ||||
chr11:506732-507023 | Common:3; Rare:98 |