Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:116526154-116526657 | Common:3; Rare:147; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr7:116672159-116672468 | Common:1; Rare:68; Clinvar:2 | ||||
chr7:117873419-117873644 | Common:1; Rare:82 | ||||
chr7:118183989-118184217 | Common:1; Rare:91 | ||||
chr7:120988776-120988850 | Rare:16 | ||||
chr7:121396273-121396616 | Common:1; Rare:115 | ||||
chr7:122144063-122144444 | Common:1; Rare:83 | ||||
chr7:122886403-122886679 | Common:1; Rare:77 | ||||
chr7:123534530-123534814 | Common:4; Rare:64 | ||||
chr7:123748710-123749258 | Common:3; Rare:197 | ||||
chr7:124929795-124929880 | Common:2; Rare:23 | ||||
chr7:127588292-127588453 | Rare:62 | ||||
chr7:127591023-127591275 | Common:1; Rare:71 | ||||
chr7:127651840-127652233 | Common:3; Rare:112 | ||||
chr7:127990857-127990987 | Rare:23 |