Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71851187-71851440 | Common:5; Rare:107; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273693-72274011 | Rare:99 | ||||
chr10:72354598-72354670 | Rare:12 | ||||
chr10:72354883-72355188 | Common:2; Rare:110 | ||||
chr10:72626041-72626364 | Common:2; Rare:78 | ||||
chr10:73096742-73097018 | Common:4; Rare:84 | ||||
chr10:73167902-73168142 | Rare:59 | ||||
chr10:73252525-73252828 | Common:2; Rare:88; Clinvar:5; Clinvar (benign):2 | ||||
chr10:73495600-73495771 | Rare:35 | ||||
chr10:73495824-73496145 | Common:2; Rare:90 | ||||
chr10:73591283-73591470 | Common:1; Rare:40 | ||||
chr10:73625955-73626152 | Rare:41 | ||||
chr10:73743996-73744430 | Common:1; Rare:109 | ||||
chr10:73772229-73772318 | Common:1; Rare:43 | ||||
chr10:73772420-73772708 | Rare:132 |