Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:56034169-56034270 | Rare:30 | ||||
chr7:56051378-56051920 | Common:1; Rare:196; Clinvar:5; Clinvar (benign):1 | ||||
chr7:56106363-56106671 | Common:8; Rare:117 | ||||
chr7:64665947-64666179 | Common:5; Rare:53 | ||||
chr7:65006625-65006838 | Common:2; Rare:63 | ||||
chr7:66114752-66114895 | Common:1; Rare:69 | ||||
chr7:66115179-66115353 | Rare:40 | ||||
chr7:66682040-66682147 | Common:4; Rare:48 | ||||
chr7:66996555-66996913 | Common:2; Rare:88 | ||||
chr7:73557585-73557763 | Common:2; Rare:65 | ||||
chr7:73683408-73683628 | Common:3; Rare:91 | ||||
chr7:73738791-73739017 | Common:1; Rare:67 | ||||
chr7:73842504-73842716 | Common:6; Rare:32 | ||||
chr7:74174080-74174441 | Common:1; Rare:164 | ||||
chr7:74254334-74254528 | Rare:90 |