Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119140610-119140785 | Common:1; Rare:61 | ||||
chr1:119648125-119648350 | Common:3; Rare:79 | ||||
chr1:120176350-120176616 | Common:1; Rare:55 | ||||
chr1:121184945-121185088 | Rare:47 | ||||
chr1:121185262-121185360 | Rare:14 | ||||
chr1:144461540-144461669 | Common:4; Rare:56 | ||||
chr1:145823882-145824286 | Rare:144 | ||||
chr1:145918680-145919048 | Common:2; Rare:84 | ||||
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958223 | Rare:52 | ||||
chr1:145964571-145964754 | Rare:47 | ||||
chr1:145995110-145995479 | Rare:149 | ||||
chr1:145995992-145996281 | Rare:129 | ||||
chr1:145996412-145996906 | Common:2; Rare:179 | ||||
chr1:147172426-147172823 | Common:1; Rare:102 |