Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93180296-93180797 | Common:4; Rare:370 | ||||
chr1:93180941-93181088 | Common:3; Rare:38 | ||||
chr1:93345594-93346001 | Common:9; Rare:244 | ||||
chr1:93448001-93448220 | Common:4; Rare:139 | ||||
chr1:93680690-93681050 | Common:3; Rare:120 | ||||
chr1:93681600-93682015 | Common:10; Rare:226 | ||||
chr1:93846115-93846473 | Common:4; Rare:171 | ||||
chr1:93847050-93847340 | Common:2; Rare:106 | ||||
chr1:93847445-93847651 | Common:2; Rare:136 | ||||
chr1:93879132-93879299 | Common:4; Rare:112 | ||||
chr1:93909390-93909509 | Rare:31 | ||||
chr1:94021210-94021530 | Rare:131; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:94237558-94237748 | Rare:149 | ||||
chr1:94418096-94418508 | Common:5; Rare:231 | ||||
chr1:94541727-94542020 | Rare:161 |