Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70170431-70170670 | Common:4; Rare:80 | ||||
chr10:70888534-70888680 | Common:2; Rare:44; Clinvar:5; Clinvar (benign):2 | ||||
chr10:71819549-71819872 | Common:1; Rare:132; Clinvar:3; Clinvar (benign):3 | ||||
chr10:72216246-72216523 | Common:3; Rare:81 | ||||
chr10:72354881-72355029 | Common:2; Rare:71 | ||||
chr10:73096794-73097024 | Common:3; Rare:72 | ||||
chr10:73167935-73168133 | Rare:51 | ||||
chr10:73252552-73252802 | Common:2; Rare:72; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73495610-73495766 | Rare:30 | ||||
chr10:73744250-73744436 | Common:1; Rare:50 | ||||
chr10:73772233-73772325 | Common:1; Rare:45 | ||||
chr10:73772625-73772814 | Rare:96 | ||||
chr10:73782005-73782332 | Common:1; Rare:106 | ||||
chr10:73811586-73811601 | Rare:2 | ||||
chr10:73874477-73874715 | Rare:57 |