Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:55964432-55964615 | Rare:60 | ||||
chr7:56051384-56051845 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):1 | ||||
chr7:56063939-56064350 | Common:2; Rare:188 | ||||
chr7:56106418-56106714 | Common:8; Rare:100 | ||||
chr7:64665985-64666183 | Common:4; Rare:43 | ||||
chr7:64794227-64794525 | Common:5; Rare:82 | ||||
chr7:64877479-64877643 | Common:1; Rare:27 | ||||
chr7:64903119-64903310 | Common:2; Rare:50 | ||||
chr7:65006616-65006878 | Common:3; Rare:79 | ||||
chr7:65982119-65982309 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr7:66075548-66075912 | Rare:98; Clinvar (benign):1 | ||||
chr7:66114732-66114960 | Common:2; Rare:97 | ||||
chr7:66205043-66205481 | Common:1; Rare:99 | ||||
chr7:66628629-66629001 | Common:2; Rare:138; Clinvar:6 | ||||
chr7:66681972-66682210 | Common:6; Rare:104 |