Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:120176377-120176621 | Common:1; Rare:53 | ||||
chr1:121184807-121185088 | Common:1; Rare:96 | ||||
chr1:145823869-145824088 | Rare:80 | ||||
chr1:145824093-145824238 | Rare:42 | ||||
chr1:145918689-145919005 | Common:2; Rare:66 | ||||
chr1:145927358-145927644 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958223 | Rare:53 | ||||
chr1:145964583-145964765 | Rare:41 | ||||
chr1:145996499-145996808 | Rare:121 | ||||
chr1:147172044-147172299 | Rare:68 | ||||
chr1:147172420-147172830 | Common:1; Rare:105 | ||||
chr1:148952031-148952141 | Common:3; Rare:28 | ||||
chr1:148952261-148952603 | Common:5; Rare:101 | ||||
chr1:149886632-149887202 | Common:3; Rare:220 | ||||
chr1:149887952-149888057 | Rare:28 |