Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119140594-119140671 | Rare:40; Clinvar (pathogenic):1 | ||||
chr1:120176377-120176598 | Rare:50 | ||||
chr1:121184926-121185060 | Rare:46 | ||||
chr1:145823922-145824268 | Rare:123 | ||||
chr1:145927364-145927670 | Common:1; Rare:83; Clinvar (pathogenic):1 | ||||
chr1:145964605-145964754 | Rare:34 | ||||
chr1:145996533-145996790 | Rare:103 | ||||
chr1:146228961-146229196 | Common:2; Rare:49 | ||||
chr1:147172440-147172779 | Common:1; Rare:84 | ||||
chr1:147541406-147541501 | Rare:12 | ||||
chr1:149103537-149103616 | Common:2; Rare:35 | ||||
chr1:149812062-149812144 | Rare:41 | ||||
chr1:149812154-149812560 | Common:2; Rare:176 | ||||
chr1:149813679-149813815 | Common:3; Rare:46 | ||||
chr1:149850820-149851064 | Rare:1 |