Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:48493606-48493883 | Common:2; Rare:54 | ||||
chr10:49941937-49942073 | Rare:33 | ||||
chr10:50067854-50067966 | Common:1; Rare:50 | ||||
chr10:50623673-50623758 | Rare:17 | ||||
chr10:50623892-50624090 | Common:1; Rare:78 | ||||
chr10:51074075-51074145 | Common:3; Rare:14 | ||||
chr10:51074390-51074618 | Common:1; Rare:53; Clinvar (benign):4 | ||||
chr10:56361211-56361500 | Common:6; Rare:104 | ||||
chr10:58385197-58385485 | Common:4; Rare:92 | ||||
chr10:59906417-59906713 | Common:2; Rare:77 | ||||
chr10:60944171-60944374 | Common:1; Rare:64 | ||||
chr10:62816341-62816495 | Rare:23 | ||||
chr10:63269155-63269388 | Common:2; Rare:50 | ||||
chr10:67838032-67838243 | Common:2; Rare:44 | ||||
chr10:68074107-68074195 | Common:1; Rare:15 |