Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:127343481-127343645 | Common:2; Rare:45 | ||||
chr6:127518889-127519076 | Common:2; Rare:30 | ||||
chr6:128520444-128520763 | Common:2; Rare:102 | ||||
chr6:129490526-129490724 | Common:1; Rare:40 | ||||
chr6:130955916-130956042 | Rare:29 | ||||
chr6:131628113-131628433 | Common:3; Rare:87 | ||||
chr6:132401417-132401595 | Common:1; Rare:55 | ||||
chr6:132814255-132814613 | Common:4; Rare:131 | ||||
chr6:133888944-133889142 | Common:1; Rare:33 | ||||
chr6:133953026-133953241 | Common:2; Rare:63 | ||||
chr6:134174852-134174977 | Common:1; Rare:54 | ||||
chr6:135054741-135054996 | Common:6; Rare:77 | ||||
chr6:135497648-135497890 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136289747-136290014 | Common:1; Rare:116 | ||||
chr6:136550395-136550687 | Common:2; Rare:83 |