Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:99919578-99919613 | Rare:12 | ||||
chr7:100088916-100089008 | Rare:31 | ||||
chr7:100101357-100101711 | Common:1; Rare:135; Clinvar (benign):1 | ||||
chr7:100119335-100119641 | Rare:78 | ||||
chr7:100428665-100428817 | Common:4; Rare:55 | ||||
chr7:100436471-100436709 | Rare:67 | ||||
chr7:100612404-100612582 | Rare:36 | ||||
chr7:100705868-100706200 | Common:4; Rare:121 | ||||
chr7:100827469-100827776 | Rare:109 | ||||
chr7:100852619-100852769 | Rare:39 | ||||
chr7:100874951-100875259 | Common:2; Rare:101 | ||||
chr7:101085352-101085499 | Common:1; Rare:28 | ||||
chr7:101217850-101218198 | Common:4; Rare:111 | ||||
chr7:101245000-101245173 | Common:1; Rare:73 | ||||
chr7:101321725-101321880 | Common:3; Rare:54 |