Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122980329-122980431 | Common:1; Rare:12 | ||||
chr10:123008791-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124418902-124419092 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125161001-125161281 | Common:4; Rare:103 | ||||
chr10:125719466-125719734 | Common:1; Rare:86 | ||||
chr10:125823200-125823585 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905302-126905465 | Rare:62 | ||||
chr10:133308835-133308989 | Rare:72 | ||||
chr11:207332-207575 | Common:6; Rare:106 | ||||
chr11:208615-208869 | Rare:93 | ||||
chr11:236331-236549 | Common:8; Rare:72 | ||||
chr11:236906-237044 | Common:1; Rare:54 | ||||
chr11:313686-314072 | Common:1; Rare:66 | ||||
chr11:506729-506981 | Common:3; Rare:86 | ||||
chr11:560710-561016 | Common:5; Rare:142 |