Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73247066-73247418 | Rare:166 | ||||
chr10:73287238-73287479 | Rare:40 | ||||
chr10:73359685-73359783 | Common:1; Rare:19 | ||||
chr10:73730456-73730595 | Common:1; Rare:37 | ||||
chr10:73732321-73732450 | Rare:22 | ||||
chr10:73765872-73766164 | Rare:70 | ||||
chr10:73945537-73945655 | Rare:30 | ||||
chr10:74070665-74071093 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):8 | ||||
chr10:74082275-74082514 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:74094124-74094449 | Common:2; Rare:74; Clinvar:5; Clinvar (benign):3 | ||||
chr10:74110866-74111001 | Common:1; Rare:24 | ||||
chr10:74112611-74112905 | Common:1; Rare:46 | ||||
chr10:74114586-74114894 | Common:1; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
chr10:74422823-74423029 | Common:1; Rare:34 | ||||
chr10:74529310-74529333 | Rare:3 |