Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73495796-73495834 | Rare:10 | ||||
chr10:73625979-73626106 | Rare:22 | ||||
chr10:73744244-73744430 | Common:1; Rare:50 | ||||
chr10:73772637-73772718 | Rare:49 | ||||
chr10:73781988-73782078 | Common:1; Rare:27 | ||||
chr10:73874473-73874718 | Rare:59 | ||||
chr10:73997732-73998374 | Common:2; Rare:161; Clinvar:4; Clinvar (benign):4 | ||||
chr10:74104861-74105183 | Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
chr10:74150761-74151293 | Common:3; Rare:132 | ||||
chr10:74826391-74826645 | Rare:62; Clinvar (benign):2 | ||||
chr10:75210437-75210867 | Common:1; Rare:152 | ||||
chr10:75401779-75401917 | Common:2; Rare:45 | ||||
chr10:77637277-77637494 | Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
chr10:77925883-77926121 | Common:3; Rare:45 | ||||
chr10:80078639-80078720 | Rare:33 |