Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:120176343-120176598 | Rare:55 | ||||
chr1:145823927-145824268 | Rare:121 | ||||
chr1:145918668-145919005 | Common:2; Rare:78; Clinvar:1 | ||||
chr1:145927400-145927628 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
chr1:145964571-145964754 | Rare:47 | ||||
chr1:145996473-145996813 | Common:1; Rare:133 | ||||
chr1:146228991-146229170 | Common:1; Rare:35 | ||||
chr1:147172427-147172791 | Common:1; Rare:95 | ||||
chr1:148679713-148679859 | Rare:18 | ||||
chr1:148952021-148952141 | Common:3; Rare:32 | ||||
chr1:148952271-148952648 | Common:5; Rare:104 | ||||
chr1:149842748-149842962 | Rare:3 | ||||
chr1:149850826-149851062 | Rare:1 | ||||
chr1:149886646-149887004 | Common:2; Rare:132 | ||||
chr1:149927764-149927901 | Common:1; Rare:55; Clinvar (benign):4 |