Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:44959636-44959834 | Common:1; Rare:66 | ||||
chr10:45000757-45000956 | Common:1; Rare:86 | ||||
chr10:45727188-45727286 | Common:1; Rare:42 | ||||
chr10:45972374-45972503 | Rare:34 | ||||
chr10:48604936-48605205 | Common:1; Rare:59 | ||||
chr10:49941943-49942073 | Rare:31 | ||||
chr10:50067852-50067985 | Common:2; Rare:58 | ||||
chr10:50623897-50624070 | Common:1; Rare:69 | ||||
chr10:51074382-51074487 | Rare:17 | ||||
chr10:52314076-52314325 | Common:1; Rare:59 | ||||
chr10:56361215-56361488 | Common:6; Rare:93 | ||||
chr10:58268945-58269282 | Common:5; Rare:109 | ||||
chr10:68332920-68332985 | Rare:17 | ||||
chr10:70233356-70233563 | Common:4; Rare:69 | ||||
chr10:71819465-71819896 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 |