Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93878414-93878814 | Common:1; Rare:92 | ||||
chr1:93879060-93879806 | Common:22; Rare:651 | ||||
chr1:93908615-93909015 | Common:1; Rare:81 | ||||
chr1:93909178-93909993 | Common:28; Rare:1014 | ||||
chr1:94417770-94418010 | Common:2; Rare:72 | ||||
chr1:94417996-94418546 | Common:11; Rare:599 | ||||
chr1:94418675-94419316 | Common:4; Rare:164 | ||||
chr1:94541666-94542074 | Common:2; Rare:323 | ||||
chr1:95072520-95072800 | Rare:135; Clinvar (benign):1 | ||||
chr1:95072820-95073460 | Common:15; Rare:526; Clinvar (benign):2 | ||||
chr1:95116705-95117154 | Rare:139 | ||||
chr1:95117205-95117483 | Rare:343 | ||||
chr1:95117468-95117870 | Common:4; Rare:229 | ||||
chr1:95233924-95234324 | Common:31; Rare:595 | ||||
chr1:96721449-96722193 | Common:14; Rare:691 |