Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44777785-44778039 | Rare:74 | ||||
chr1:44986551-44986767 | Common:2; Rare:39; Clinvar (benign):1 | ||||
chr1:45500025-45500351 | Common:2; Rare:78; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45583958-45584046 | Rare:32 | ||||
chr1:45688059-45688237 | Common:1; Rare:52 | ||||
chr1:46198353-46198495 | Common:1; Rare:59; Clinvar:1 | ||||
chr1:46303323-46303715 | Common:2; Rare:100 | ||||
chr1:52055217-52055310 | Rare:27 | ||||
chr1:52056174-52056335 | Rare:49 | ||||
chr1:52404460-52404624 | Common:1; Rare:48 | ||||
chr1:52553086-52553364 | Common:4; Rare:76 | ||||
chr1:53946287-53946479 | Rare:69 | ||||
chr1:54053198-54053638 | Common:6; Rare:143 | ||||
chr1:54200008-54200207 | Rare:40 | ||||
chr1:66924840-66925021 | Rare:77 |