Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160284983-160285400 | Common:10; Rare:296; Clinvar:10; Clinvar (benign):12 | ||||
chr1:160343147-160343869 | Common:10; Rare:1140 | ||||
chr1:160366757-160367165 | Common:15; Rare:246 | ||||
chr1:160400240-160400790 | Common:8; Rare:337 | ||||
chr1:160522895-160523349 | Rare:139 | ||||
chr1:160578565-160580430 | Common:19; Rare:649 | ||||
chr1:160646180-160646560 | Common:2; Rare:67 | ||||
chr1:160739157-160739281 | Rare:37 | ||||
chr1:161020640-161021040 | Rare:571 | ||||
chr1:161021060-161021640 | Common:25; Rare:735 | ||||
chr1:161044890-161045610 | Common:4; Rare:248 | ||||
chr1:161045794-161046502 | Common:7; Rare:549 | ||||
chr1:161117357-161118807 | Common:9; Rare:1175 | ||||
chr1:161119324-161120057 | Common:3; Rare:243 | ||||
chr1:161131785-161133688 | Common:18; Rare:1075 |