Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43946571-43946983 | Rare:108 | ||||
chr1:44218459-44218702 | Rare:75 | ||||
chr1:44674413-44674733 | Common:3; Rare:84 | ||||
chr1:44775480-44775607 | Rare:50 | ||||
chr1:44775833-44776139 | Common:2; Rare:111 | ||||
chr1:44986532-44986680 | Common:2; Rare:29; Clinvar (benign):1 | ||||
chr1:45012176-45012278 | Rare:40; Clinvar:4 | ||||
chr1:45339957-45340182 | Rare:73 | ||||
chr1:45340386-45340460 | Common:1; Rare:18; Clinvar:1 | ||||
chr1:45500016-45500335 | Common:2; Rare:73; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr1:45550730-45550898 | Common:1; Rare:43 | ||||
chr1:45583931-45584060 | Rare:47 | ||||
chr1:45686466-45686657 | Rare:66 | ||||
chr1:45687050-45687353 | Common:1; Rare:81 | ||||
chr1:45688055-45688211 | Common:1; Rare:39 |