Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32650415-32650689 | Common:3; Rare:222 | ||||
chr1:32650899-32651334 | Common:6; Rare:456 | ||||
chr1:32702660-32703470 | Common:6; Rare:249 | ||||
chr1:32741729-32742097 | Common:4; Rare:160 | ||||
chr1:32753735-32754312 | Common:12; Rare:422 | ||||
chr1:32816673-32817073 | Common:3; Rare:101 | ||||
chr1:32817196-32817744 | Common:3; Rare:410; Clinvar:15; Clinvar (benign):8 | ||||
chr1:32818119-32818310 | Common:1; Rare:96 | ||||
chr1:32818258-32818401 | Rare:39 | ||||
chr1:32892649-32893500 | Common:28; Rare:432 | ||||
chr1:32893444-32893850 | Common:2; Rare:211; Clinvar (pathogenic):1 | ||||
chr1:32901241-32901601 | Common:3; Rare:188 | ||||
chr1:32964745-32965075 | Common:6; Rare:289 | ||||
chr1:33036777-33037179 | Rare:241; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:33080815-33081275 | Common:13; Rare:380 |