Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69179918-69180312 | Common:3; Rare:126 | ||||
chr10:69220185-69220413 | Rare:45 | ||||
chr10:70132736-70132906 | Rare:48 | ||||
chr10:70170448-70170711 | Common:3; Rare:84 | ||||
chr10:70233338-70233562 | Common:5; Rare:80 | ||||
chr10:70403971-70404193 | Rare:84 | ||||
chr10:71819514-71819894 | Common:1; Rare:157; Clinvar:5; Clinvar (benign):3 | ||||
chr10:71851161-71851464 | Common:5; Rare:126; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216237-72216499 | Common:2; Rare:79 | ||||
chr10:72273662-72274015 | Rare:106 | ||||
chr10:72354889-72355196 | Common:2; Rare:111 | ||||
chr10:73096804-73097182 | Common:4; Rare:110 | ||||
chr10:73167922-73168141 | Rare:53 | ||||
chr10:73252576-73252802 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):1 | ||||
chr10:73358728-73358876 | Common:2; Rare:35 |