Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25338190-25338532 | Common:2; Rare:116 | ||||
chr1:25819861-25820248 | Common:5; Rare:114 | ||||
chr1:25820806-25820870 | Common:1; Rare:15 | ||||
chr1:25859359-25859580 | Common:3; Rare:93 | ||||
chr1:26021491-26021789 | Common:2; Rare:46 | ||||
chr1:26111063-26111234 | Rare:51 | ||||
chr1:26279933-26280198 | Rare:144 | ||||
chr1:26432105-26432422 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472304-26472621 | Common:4; Rare:120 | ||||
chr1:26473020-26473306 | Common:1; Rare:149 | ||||
chr1:26545707-26545866 | Common:1; Rare:32 | ||||
chr1:26787877-26788237 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890220-26890359 | Common:1; Rare:52 | ||||
chr1:26900043-26900224 | Rare:68 | ||||
chr1:26900411-26900553 | Rare:52 |