Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:74120996-74121260 | Common:1; Rare:88; Clinvar:1 | ||||
chr7:74526028-74526311 | Common:2; Rare:59 | ||||
chr7:74890513-74890820 | Common:3; Rare:98 | ||||
chr7:75779111-75779280 | Rare:33 | ||||
chr7:76297588-76297763 | Common:2; Rare:41 | ||||
chr7:76580230-76580255 | Rare:4 | ||||
chr7:91266453-91266745 | Common:1; Rare:92 | ||||
chr7:98315556-98315779 | Common:9; Rare:71; Clinvar (benign):1 | ||||
chr7:99652735-99652964 | Common:2; Rare:45 | ||||
chr7:100030109-100030298 | Rare:46 | ||||
chr7:100124542-100124732 | Common:2; Rare:70 | ||||
chr7:100335846-100336146 | Common:1; Rare:100 | ||||
chr7:105013025-105013207 | Common:1; Rare:65 | ||||
chr7:105013552-105013671 | Rare:46 | ||||
chr7:105106270-105106352 | Rare:18 |