Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:93702423-93702614 | Common:5; Rare:76 | ||||
chr10:93757663-93758125 | Common:1; Rare:78; Clinvar:4; Clinvar (benign):2 | ||||
chr10:94362892-94363027 | Common:3; Rare:52 | ||||
chr10:95290922-95291196 | Common:2; Rare:112 | ||||
chr10:95561334-95561590 | Common:4; Rare:72 | ||||
chr10:95656652-95656878 | Rare:66; Clinvar:5 | ||||
chr10:95693879-95694188 | Common:5; Rare:101; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:95907756-95907940 | Common:2; Rare:51 | ||||
chr10:95908122-95908244 | Rare:23 | ||||
chr10:96129696-96129732 | Rare:10 | ||||
chr10:96129984-96130340 | Common:4; Rare:119 | ||||
chr10:96130384-96130540 | Common:1; Rare:47 | ||||
chr10:96831994-96832298 | Rare:118 | ||||
chr10:97426055-97426300 | Common:2; Rare:104 | ||||
chr10:97445983-97446217 | Rare:60 |