Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:125649393-125649736 | Common:3; Rare:56 | ||||
chr9:126719653-126719892 | Rare:41 | ||||
chr9:127836040-127836179 | Rare:35 | ||||
chr9:127843125-127843442 | Common:2; Rare:70; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr9:127863390-127863636 | Rare:35 | ||||
chr9:128684428-128684547 | Rare:21 | ||||
chr9:129488485-129488783 | Common:2; Rare:83 | ||||
chr9:129773690-129773999 | Common:2; Rare:57 | ||||
chr9:129812722-129813069 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
chr9:129885833-129886022 | Common:1; Rare:34 | ||||
chr9:129892883-129893041 | Rare:31 | ||||
chr9:131635310-131635656 | Common:3; Rare:64 | ||||
chr9:131645302-131645457 | Rare:20 | ||||
chr9:131650456-131650712 | Common:1; Rare:35 | ||||
chr9:131658455-131658599 | Common:1; Rare:21 |