Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119140640-119140735 | Rare:25 | ||||
chr1:120176343-120176596 | Rare:55 | ||||
chr1:145607871-145608004 | Common:2; Rare:28 | ||||
chr1:145823937-145824249 | Rare:112 | ||||
chr1:145918667-145919022 | Common:2; Rare:86; Clinvar:1 | ||||
chr1:145927422-145927667 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:146229001-146229115 | Common:1; Rare:28 | ||||
chr1:147172450-147172808 | Common:1; Rare:91 | ||||
chr1:147242518-147242715 | Common:3; Rare:71 | ||||
chr1:148952021-148952115 | Common:3; Rare:26 | ||||
chr1:149886668-149886953 | Rare:91 | ||||
chr1:149887947-149888215 | Rare:62 | ||||
chr1:149927767-149927912 | Common:1; Rare:53; Clinvar (benign):4 | ||||
chr1:150067688-150067866 | Rare:57 | ||||
chr1:150272392-150272747 | Common:1; Rare:61 |