Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:75235153-75235870 | Common:16; Rare:588 | ||||
chr10:75235911-75236381 | Common:7; Rare:241 | ||||
chr10:75431251-75431735 | Common:7; Rare:185 | ||||
chr10:77925359-77926093 | Common:4; Rare:217 | ||||
chr10:77926092-77926518 | Rare:240 | ||||
chr10:77926578-77926978 | Common:6; Rare:353 | ||||
chr10:77927000-77927410 | Common:3; Rare:111 | ||||
chr10:78028976-78029376 | Common:3; Rare:89 | ||||
chr10:78029398-78029798 | Common:13; Rare:450; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
chr10:78029877-78030145 | Common:1; Rare:51 | ||||
chr10:78033509-78033943 | Common:13; Rare:589; Clinvar (benign):20 | ||||
chr10:78033995-78034614 | Common:9; Rare:308 | ||||
chr10:78035517-78035641 | Common:1; Rare:26; Clinvar (benign):3 | ||||
chr10:79068397-79069732 | Common:31; Rare:1028 | ||||
chr10:79346809-79347209 | Common:3; Rare:105 |