Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161198636-161198668 | Rare:4 | ||||
chr1:161201559-161201693 | Rare:28 | ||||
chr1:161201925-161202499 | Common:4; Rare:159; Clinvar:5; Clinvar (benign):10 | ||||
chr1:161202593-161202770 | Common:2; Rare:31 | ||||
chr1:161202787-161202951 | Rare:29 | ||||
chr1:161225697-161226129 | Common:10; Rare:77 | ||||
chr1:161226464-161226522 | Rare:23 | ||||
chr1:161226692-161227045 | Rare:82 | ||||
chr1:161227465-161227655 | Rare:37 | ||||
chr1:161313531-161313764 | Common:1; Rare:49 | ||||
chr1:161314041-161314530 | Common:5; Rare:150; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:161314775-161315006 | Common:1; Rare:53 | ||||
chr1:161523905-161524155 | Common:9; Rare:90 | ||||
chr1:161524227-161524483 | Common:3; Rare:75 | ||||
chr1:161524520-161524590 | Common:2; Rare:17 |