Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43358662-43359006 | Common:7; Rare:110 | ||||
chr1:43367953-43368149 | Rare:48 | ||||
chr1:43389733-43389945 | Common:3; Rare:95 | ||||
chr1:43946585-43946987 | Rare:107 | ||||
chr1:44213341-44213527 | Common:1; Rare:36 | ||||
chr1:44674425-44674739 | Common:3; Rare:78 | ||||
chr1:44775473-44775620 | Common:1; Rare:62 | ||||
chr1:44775811-44776164 | Common:2; Rare:125 | ||||
chr1:44808430-44808572 | Rare:38 | ||||
chr1:45339996-45340041 | Rare:12 | ||||
chr1:45340103-45340193 | Rare:39 | ||||
chr1:45340376-45340502 | Common:2; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
chr1:45499998-45500335 | Common:2; Rare:75; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr1:45521874-45522064 | Common:1; Rare:75 | ||||
chr1:45550721-45551076 | Common:3; Rare:89 |