Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:168422501-168422865 | Common:1; Rare:48 | ||||
chr1:169087039-169087309 | Common:2; Rare:55 | ||||
chr1:169109830-169109972 | Rare:36 | ||||
chr1:174022911-174023024 | Rare:18 | ||||
chr1:176801042-176801318 | Common:1; Rare:45 | ||||
chr1:178371317-178371661 | Common:8; Rare:90 | ||||
chr1:178371931-178372006 | Rare:11 | ||||
chr1:178372023-178372279 | Rare:53 | ||||
chr1:178542660-178542831 | Common:6; Rare:53 | ||||
chr1:180926643-180926840 | Common:3; Rare:42 | ||||
chr1:181099461-181099737 | Common:2; Rare:46 | ||||
chr1:181510562-181510783 | Common:1; Rare:52 | ||||
chr1:183261053-183261263 | Rare:50; Clinvar (pathogenic):1 | ||||
chr1:183417329-183417393 | Rare:18 | ||||
chr1:183443194-183443282 | Rare:14 |