Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230824810-230825540 | Common:2; Rare:195 | ||||
chr1:230863473-230863873 | Common:3; Rare:97 | ||||
chr1:231139860-231140350 | Common:5; Rare:90 | ||||
chr1:231172257-231172928 | Common:8; Rare:229 | ||||
chr1:231420928-231421328 | Rare:140; Clinvar:2; Clinvar (benign):2 | ||||
chr1:231421248-231421907 | Common:5; Rare:366; Clinvar:20; Clinvar (benign):14 | ||||
chr1:231422173-231422660 | Common:18; Rare:477; Clinvar:18; Clinvar (benign):18 | ||||
chr1:231422602-231422754 | Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr1:231778002-231778391 | Common:3; Rare:73 | ||||
chr1:231986585-231987351 | Common:10; Rare:242 | ||||
chr1:232192480-232192770 | Common:1; Rare:58 | ||||
chr1:232248146-232248986 | Common:10; Rare:245 | ||||
chr1:232250578-232251148 | Common:1; Rare:190 | ||||
chr1:232261068-232261196 | Rare:30 | ||||
chr1:232283828-232284125 | Common:2; Rare:49 |