Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:92134741-92134810 | Common:1; Rare:12 | ||||
chr7:92245880-92245994 | Rare:32; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92246042-92246447 | Common:4; Rare:130; Clinvar:1; Clinvar (benign):1 | ||||
chr7:92528428-92528816 | Common:3; Rare:125; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr7:92836243-92836498 | Rare:43 | ||||
chr7:93117886-93118098 | Rare:32 | ||||
chr7:94004303-94004472 | Rare:49 | ||||
chr7:94394556-94395006 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
chr7:94395011-94395102 | Rare:24; Clinvar (benign):2 | ||||
chr7:94425743-94426050 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr7:94656118-94656372 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr7:97117479-97117759 | Common:1; Rare:120 | ||||
chr7:97872394-97872518 | Rare:43 | ||||
chr7:98252208-98252402 | Common:1; Rare:47 | ||||
chr7:99325814-99325983 | Common:1; Rare:64 |