Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:92325605-92326019 | Common:4; Rare:123 | ||||
chr9:92669990-92670427 | Common:1; Rare:143 | ||||
chr9:93451455-93451702 | Common:3; Rare:69 | ||||
chr9:93452288-93452377 | Rare:13 | ||||
chr9:95317663-95317836 | Common:1; Rare:53; Clinvar:2 | ||||
chr9:95875453-95875732 | Common:1; Rare:98 | ||||
chr9:95875961-95876041 | Common:4; Rare:40 | ||||
chr9:96655307-96655389 | Rare:19 | ||||
chr9:96778054-96778154 | Rare:32 | ||||
chr9:97633302-97633488 | Common:2; Rare:51 | ||||
chr9:97633572-97633862 | Common:3; Rare:95 | ||||
chr9:97922471-97922609 | Common:3; Rare:64 | ||||
chr9:99221916-99222364 | Common:2; Rare:177; Clinvar:2; Clinvar (benign):2 | ||||
chr9:99906583-99906711 | Rare:61 | ||||
chr9:100098951-100099323 | Common:3; Rare:107; Clinvar:2 |