Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:28686027-28686166 | Rare:38 | ||||
chr7:28958304-28958510 | Rare:58 | ||||
chr7:30478681-30478857 | Common:1; Rare:69; Clinvar:1 | ||||
chr7:30504745-30505103 | Common:2; Rare:121 | ||||
chr7:30594717-30594916 | Common:2; Rare:88; Clinvar:5; Clinvar (benign):4 | ||||
chr7:32070843-32071131 | Common:3; Rare:74 | ||||
chr7:32495272-32495591 | Common:1; Rare:81 | ||||
chr7:33062714-33062905 | Common:3; Rare:84 | ||||
chr7:33129232-33129570 | Common:5; Rare:95 | ||||
chr7:35695133-35695216 | Rare:20 | ||||
chr7:35800901-35801254 | Common:2; Rare:147 | ||||
chr7:39566350-39566450 | Common:1; Rare:50 | ||||
chr7:39623394-39623819 | Rare:141 | ||||
chr7:40134581-40135035 | Rare:141; Clinvar:1 | ||||
chr7:42932163-42932411 | Rare:100 |