Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:67302394-67302737 | Common:5; Rare:110 | ||||
chr7:72829287-72829602 | Rare:89 | ||||
chr7:72954713-72954805 | Rare:16 | ||||
chr7:73005862-73006140 | Rare:29 | ||||
chr7:74045031-74045241 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
chr7:74120995-74121194 | Common:1; Rare:68; Clinvar:1 | ||||
chr7:74890520-74890846 | Common:4; Rare:108 | ||||
chr7:75359018-75359253 | Rare:6 | ||||
chr7:75639171-75639372 | Common:1; Rare:49 | ||||
chr7:76317998-76318266 | Common:7; Rare:66 | ||||
chr7:88218868-88219157 | Rare:75 | ||||
chr7:94397879-94398051 | Rare:20 | ||||
chr7:94404553-94404747 | Rare:46; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr7:94409288-94409608 | Rare:96; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr7:94409977-94410526 | Common:2; Rare:111; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 |