Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:99919490-99919657 | Rare:55 | ||||
chr7:100101352-100101711 | Common:1; Rare:137; Clinvar (benign):1 | ||||
chr7:100119284-100119742 | Rare:142; Clinvar:1 | ||||
chr7:100148687-100149049 | Common:1; Rare:159 | ||||
chr7:100428664-100428881 | Common:4; Rare:90 | ||||
chr7:100436070-100436379 | Common:1; Rare:114 | ||||
chr7:100586116-100586286 | Common:1; Rare:61 | ||||
chr7:100687567-100687879 | Common:1; Rare:98 | ||||
chr7:100852619-100852771 | Rare:41 | ||||
chr7:100874955-100875229 | Common:2; Rare:95 | ||||
chr7:101217850-101218214 | Common:4; Rare:117 | ||||
chr7:101245000-101245168 | Common:1; Rare:72 | ||||
chr7:102464844-102464978 | Common:1; Rare:58 | ||||
chr7:102748704-102749041 | Common:2; Rare:81 | ||||
chr7:103344716-103344968 | Common:1; Rare:66 |