Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96265959-96266348 | Common:2; Rare:118; Clinvar:1 | ||||
chr2:97645780-97646122 | Common:3; Rare:107 | ||||
chr2:97663892-97664205 | Common:1; Rare:110 | ||||
chr2:98608397-98608649 | Common:1; Rare:110; Clinvar (benign):1 | ||||
chr2:99154877-99155031 | Common:1; Rare:62 | ||||
chr2:99180971-99181226 | Common:2; Rare:76 | ||||
chr2:99337253-99337568 | Rare:114 | ||||
chr2:100562629-100563050 | Common:5; Rare:123 | ||||
chr2:101252658-101252907 | Common:5; Rare:82 | ||||
chr2:101308212-101308292 | Rare:25 | ||||
chr2:102104391-102104853 | Common:9; Rare:112 | ||||
chr2:102142644-102142965 | Common:5; Rare:95 | ||||
chr2:102187742-102187889 | Common:1; Rare:50 | ||||
chr2:102355700-102355864 | Common:2; Rare:47 | ||||
chr2:102736851-102736943 | Common:1; Rare:34 |