Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674421-44674698 | Common:3; Rare:79 | ||||
chr1:44739689-44739905 | Common:1; Rare:82 | ||||
chr1:44775458-44775607 | Rare:58 | ||||
chr1:44775783-44776140 | Common:2; Rare:131 | ||||
chr1:44986532-44986812 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr1:45339974-45340178 | Rare:61 | ||||
chr1:45500005-45500358 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521818-45522093 | Common:1; Rare:101 | ||||
chr1:45550721-45551098 | Common:3; Rare:92 | ||||
chr1:45583931-45584078 | Rare:57 | ||||
chr1:45687050-45687357 | Common:1; Rare:81 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:45750607-45750831 | Rare:80 | ||||
chr1:46132626-46132845 | Rare:70 | ||||
chr1:46132853-46133232 | Common:3; Rare:107 |