Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:93702432-93702690 | Common:5; Rare:92 | ||||
chr10:93757694-93758063 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr10:94362881-94363046 | Common:3; Rare:65 | ||||
chr10:94402352-94402502 | Rare:43 | ||||
chr10:94545626-94545892 | Common:4; Rare:84 | ||||
chr10:95194200-95194241 | Rare:3 | ||||
chr10:95290931-95291196 | Common:2; Rare:108 | ||||
chr10:95561334-95561572 | Common:3; Rare:65 | ||||
chr10:95693877-95694188 | Common:5; Rare:102; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr10:95907787-95907967 | Common:3; Rare:59 | ||||
chr10:95908134-95908238 | Rare:23 | ||||
chr10:96129932-96130059 | Common:1; Rare:48 | ||||
chr10:96130229-96130564 | Common:1; Rare:114 | ||||
chr10:97426052-97426302 | Common:2; Rare:110 | ||||
chr10:97445975-97446229 | Rare:67 |