Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775462-44775607 | Rare:55 | ||||
chr1:44775835-44776140 | Common:2; Rare:111 | ||||
chr1:44808436-44808581 | Rare:42 | ||||
chr1:44986545-44986770 | Common:2; Rare:41; Clinvar (benign):1 | ||||
chr1:45339960-45340178 | Rare:69 | ||||
chr1:45340388-45340523 | Common:1; Rare:34; Clinvar:1 | ||||
chr1:45500056-45500351 | Common:1; Rare:73; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522074 | Common:1; Rare:98 | ||||
chr1:45550721-45551078 | Common:3; Rare:89 | ||||
chr1:45687054-45687357 | Common:1; Rare:80 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:45750606-45750823 | Rare:79 | ||||
chr1:46198353-46198552 | Common:4; Rare:96; Clinvar:1 | ||||
chr1:46303138-46303775 | Common:3; Rare:189 | ||||
chr1:46340606-46340826 | Common:3; Rare:59 |