Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45340114-45340227 | Rare:52; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:45340388-45340579 | Common:1; Rare:46; Clinvar:1 | ||||
chr1:45499954-45500385 | Common:2; Rare:110; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521818-45522074 | Common:1; Rare:98 | ||||
chr1:45550719-45551121 | Common:3; Rare:97 | ||||
chr1:45583940-45584171 | Rare:89 | ||||
chr1:45686466-45686691 | Rare:83 | ||||
chr1:45687041-45687353 | Common:1; Rare:82 | ||||
chr1:45688049-45688265 | Common:1; Rare:59 | ||||
chr1:45750615-45750815 | Rare:73 | ||||
chr1:46198358-46198540 | Common:1; Rare:73; Clinvar:1 | ||||
chr1:46303207-46303775 | Common:2; Rare:176 | ||||
chr1:46340606-46340847 | Common:3; Rare:68 | ||||
chr1:46604201-46604449 | Common:1; Rare:64 | ||||
chr1:46940800-46941004 | Rare:44 |