Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226680188-226680325 | Common:2; Rare:29 | ||||
chr1:226703520-226703648 | Rare:45 | ||||
chr1:226943122-226943349 | Rare:44 | ||||
chr1:227542163-227542478 | Common:1; Rare:64 | ||||
chr1:227946265-227946294 | Rare:8 | ||||
chr1:227946810-227946926 | Rare:29 | ||||
chr1:228378371-228378742 | Common:2; Rare:156 | ||||
chr1:229221577-229221885 | Common:2; Rare:49 | ||||
chr1:229431440-229431925 | Common:5; Rare:130; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
chr1:229432268-229432884 | Common:4; Rare:134; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
chr1:230236291-230236414 | Common:2; Rare:32 | ||||
chr1:230999847-231000159 | Common:1; Rare:50 | ||||
chr1:231370666-231370953 | Common:2; Rare:62 | ||||
chr1:231421007-231421132 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
chr1:232630473-232630663 | Rare:54 |