Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43389752-43389940 | Common:3; Rare:85 | ||||
chr1:43946622-43946977 | Rare:97 | ||||
chr1:43974778-43974986 | Common:3; Rare:59 | ||||
chr1:44213348-44213540 | Common:1; Rare:39 | ||||
chr1:44674413-44674744 | Common:3; Rare:88 | ||||
chr1:44775499-44775607 | Rare:47 | ||||
chr1:44775848-44776140 | Common:2; Rare:108 | ||||
chr1:45339957-45340206 | Rare:90; Clinvar (benign):1 | ||||
chr1:45340408-45340445 | Common:1; Rare:4; Clinvar:1 | ||||
chr1:45491047-45491260 | Common:2; Rare:68 | ||||
chr1:45500239-45500356 | Rare:28; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr1:45521827-45521957 | Common:1; Rare:57 | ||||
chr1:45550704-45551112 | Common:3; Rare:103 | ||||
chr1:45583878-45584060 | Common:1; Rare:65 | ||||
chr1:45686499-45686625 | Rare:41 |