Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:66493543-66493741 | Common:3; Rare:83 | ||||
chr7:66592339-66592437 | Common:2; Rare:35 | ||||
chr7:66654275-66654567 | Common:2; Rare:92 | ||||
chr7:67302389-67302696 | Common:5; Rare:98 | ||||
chr7:72954721-72954824 | Rare:13 | ||||
chr7:73005862-73006148 | Rare:29 | ||||
chr7:74890560-74890838 | Common:2; Rare:87 | ||||
chr7:94397757-94398071 | Common:1; Rare:56; Clinvar (benign):2 | ||||
chr7:94409318-94409819 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr7:94410238-94410526 | Rare:62; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr7:94420388-94420656 | Rare:73; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr7:97972261-97972406 | Rare:35 | ||||
chr7:98472648-98472732 | Rare:23 | ||||
chr7:100335836-100336146 | Common:1; Rare:103 | ||||
chr7:105013040-105013199 | Rare:58 |