Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:51236184-51236329 | Common:2; Rare:52 | ||||
chr1:51519227-51519538 | Common:9; Rare:105 | ||||
chr1:51729484-51729921 | Common:3; Rare:116 | ||||
chr1:51878267-51878378 | Rare:38 | ||||
chr1:51878379-51879060 | Common:5; Rare:221 | ||||
chr1:52055114-52055272 | Common:1; Rare:42 | ||||
chr1:52056018-52056334 | Common:2; Rare:77 | ||||
chr1:52141864-52142187 | Rare:88 | ||||
chr1:52366085-52366239 | Common:1; Rare:45 | ||||
chr1:52404357-52404826 | Common:2; Rare:131 | ||||
chr1:52553055-52553395 | Common:4; Rare:97 | ||||
chr1:52632961-52633013 | Rare:10 | ||||
chr1:52698035-52698206 | Common:1; Rare:41 | ||||
chr1:52698237-52698384 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:52842645-52842886 | Common:1; Rare:92 |