Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52404462-52404649 | Common:1; Rare:56 | ||||
chr1:52552898-52553387 | Common:4; Rare:144 | ||||
chr1:52553434-52553685 | Common:3; Rare:71 | ||||
chr1:52602263-52602433 | Common:2; Rare:54 | ||||
chr1:52633481-52633572 | Rare:36 | ||||
chr1:52698324-52698450 | Common:2; Rare:43 | ||||
chr1:52927170-52927352 | Common:4; Rare:54 | ||||
chr1:53196664-53196800 | Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
chr1:53220504-53220663 | Common:2; Rare:81 | ||||
chr1:53238444-53238602 | Common:1; Rare:68 | ||||
chr1:53327907-53328242 | Common:2; Rare:89 | ||||
chr1:53889715-53889974 | Common:2; Rare:82 | ||||
chr1:53894137-53894342 | Common:1; Rare:48 | ||||
chr1:53945562-53946055 | Common:8; Rare:127 | ||||
chr1:53946247-53946509 | Common:2; Rare:91 |