Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:63521779-63521995 | Common:4; Rare:83 | ||||
chr10:68074722-68074906 | Rare:39 | ||||
chr10:68075161-68075476 | Common:4; Rare:127 | ||||
chr10:68231514-68231626 | Rare:42; Clinvar (pathogenic):1 | ||||
chr10:68331588-68331725 | Rare:28 | ||||
chr10:68331899-68332179 | Common:2; Rare:113 | ||||
chr10:68332867-68332962 | Common:1; Rare:28 | ||||
chr10:68407185-68407392 | Common:4; Rare:71 | ||||
chr10:68471849-68472033 | Common:1; Rare:94; Clinvar (benign):2 | ||||
chr10:68527417-68527624 | Common:3; Rare:73 | ||||
chr10:68560213-68560451 | Rare:48 | ||||
chr10:68721000-68721062 | Rare:21 | ||||
chr10:68721090-68721534 | Common:5; Rare:132 | ||||
chr10:68901040-68901377 | Common:3; Rare:130 | ||||
chr10:68956061-68956450 | Common:3; Rare:116 |