Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43358666-43359006 | Common:7; Rare:107 | ||||
chr1:43367989-43368203 | Rare:57 | ||||
chr1:43389763-43389945 | Common:3; Rare:78 | ||||
chr1:43974587-43975046 | Common:3; Rare:108 | ||||
chr1:44674413-44674744 | Common:3; Rare:88 | ||||
chr1:44775478-44775599 | Rare:49 | ||||
chr1:44775838-44776140 | Common:2; Rare:109 | ||||
chr1:45340103-45340236 | Rare:58; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45500090-45500369 | Common:1; Rare:70; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45550730-45551102 | Common:3; Rare:90 | ||||
chr1:45583714-45584060 | Common:1; Rare:104 | ||||
chr1:45687058-45687286 | Common:1; Rare:64 | ||||
chr1:45688038-45688211 | Common:1; Rare:41 | ||||
chr1:45750622-45750808 | Rare:69 | ||||
chr1:46132627-46132774 | Rare:52 |