Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145858996-145859173 | Rare:51 | ||||
chr1:145918670-145919022 | Common:2; Rare:85; Clinvar:1 | ||||
chr1:145927415-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964593-145964747 | Rare:34 | ||||
chr1:145996514-145996796 | Rare:111 | ||||
chr1:147172450-147172779 | Common:1; Rare:82 | ||||
chr1:148951741-148952049 | Common:2; Rare:58 | ||||
chr1:148952264-148952396 | Common:1; Rare:42 | ||||
chr1:149850820-149851062 | Rare:1 | ||||
chr1:149886639-149887004 | Common:2; Rare:137 | ||||
chr1:149887873-149888215 | Rare:106 | ||||
chr1:149927760-149927906 | Common:1; Rare:59; Clinvar (benign):4 | ||||
chr1:150067690-150067860 | Rare:54 | ||||
chr1:150235928-150236366 | Common:1; Rare:98 | ||||
chr1:150282309-150282591 | Common:3; Rare:54 |