Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:92245890-92245974 | Rare:25; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92528402-92528808 | Common:3; Rare:125; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr7:93232194-93232381 | Common:2; Rare:36 | ||||
chr7:93890736-93890942 | Common:2; Rare:48 | ||||
chr7:94425748-94426050 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr7:94656083-94656372 | Common:2; Rare:76; Clinvar:3; Clinvar (benign):3 | ||||
chr7:95596507-95596682 | Common:2; Rare:34 | ||||
chr7:99325587-99325968 | Common:1; Rare:131 | ||||
chr7:99408545-99408684 | Common:2; Rare:47 | ||||
chr7:99408824-99409032 | Common:1; Rare:67 | ||||
chr7:99438722-99438977 | Common:1; Rare:80 | ||||
chr7:99466122-99466284 | Rare:55 | ||||
chr7:99558528-99558876 | Common:3; Rare:100 | ||||
chr7:100049752-100049823 | Rare:35 | ||||
chr7:100088916-100089033 | Common:1; Rare:42 |