Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:86958910-86959470 | Common:21; Rare:431 | ||||
chr10:87093215-87094027 | Common:1; Rare:223 | ||||
chr10:87093937-87094340 | Rare:298 | ||||
chr10:87094757-87095280 | Common:7; Rare:712; Clinvar:18 | ||||
chr10:87095285-87095685 | Common:5; Rare:165 | ||||
chr10:87504519-87505053 | Common:23; Rare:810; Clinvar (pathogenic):1 | ||||
chr10:87504954-87505690 | Rare:669; Clinvar (pathogenic):1 | ||||
chr10:87817297-87817697 | Rare:82 | ||||
chr10:87817910-87818040 | Rare:40 | ||||
chr10:87818060-87818700 | Common:7; Rare:442 | ||||
chr10:87861990-87862991 | Common:4; Rare:422; Clinvar:1 | ||||
chr10:87863131-87863686 | Common:9; Rare:600; Clinvar:355; Clinvar (benign):40 | ||||
chr10:87863623-87865230 | Common:8; Rare:641; Clinvar:80; Clinvar (benign):48; Clinvar (pathogenic):2 | ||||
chr10:88582635-88583020 | Common:4; Rare:180 | ||||
chr10:88880356-88880786 | Common:4; Rare:189 |