Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:125164503-125164748 | Rare:47 | ||||
chr11:125592478-125592939 | Common:6; Rare:153; Clinvar (benign):1 | ||||
chr11:125625864-125626003 | Rare:45 | ||||
chr11:125887480-125887737 | Common:2; Rare:82 | ||||
chr11:126211610-126211817 | Rare:96 | ||||
chr11:126268769-126269214 | Common:2; Rare:173; Clinvar:3; Clinvar (benign):4 | ||||
chr11:126283013-126283136 | Common:1; Rare:49 | ||||
chr11:126304004-126304105 | Rare:56 | ||||
chr11:126355526-126355760 | Common:2; Rare:64 | ||||
chr11:126405406-126405657 | Common:2; Rare:45 | ||||
chr11:126406953-126407250 | Rare:74 | ||||
chr11:128522257-128522596 | Common:3; Rare:105 | ||||
chr11:129279476-129279756 | Common:3; Rare:119 | ||||
chr11:129375598-129375653 | Rare:11 | ||||
chr11:129375692-129376019 | Common:2; Rare:94 |