Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:62816336-62816558 | Rare:39 | ||||
chr10:62816660-62816828 | Rare:35 | ||||
chr10:63133044-63133435 | Common:2; Rare:125 | ||||
chr10:63133547-63133609 | Rare:16 | ||||
chr10:63133647-63133983 | Common:2; Rare:67 | ||||
chr10:63268802-63269017 | Common:1; Rare:45 | ||||
chr10:63269148-63269434 | Common:2; Rare:61 | ||||
chr10:63465132-63465534 | Common:4; Rare:163; Clinvar (benign):1 | ||||
chr10:63465652-63465741 | Common:1; Rare:48 | ||||
chr10:63465838-63466185 | Common:4; Rare:163 | ||||
chr10:63466298-63466406 | Rare:25 | ||||
chr10:63520736-63520908 | Common:1; Rare:31 | ||||
chr10:63520927-63520997 | Rare:16 | ||||
chr10:63521115-63521531 | Common:7; Rare:143 | ||||
chr10:63521705-63522138 | Common:4; Rare:124 |