Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96208267-96208418 | Rare:76 | ||||
chr2:96208776-96208879 | Common:3; Rare:47 | ||||
chr2:96265959-96266283 | Common:2; Rare:98; Clinvar:1 | ||||
chr2:96816160-96816248 | Rare:26 | ||||
chr2:97663997-97664267 | Rare:76 | ||||
chr2:98608416-98608620 | Common:1; Rare:88; Clinvar (benign):1 | ||||
chr2:99154940-99155060 | Common:1; Rare:46; Clinvar (benign):2 | ||||
chr2:99180985-99181226 | Common:2; Rare:71 | ||||
chr2:105337407-105337564 | Common:3; Rare:69 | ||||
chr2:108534204-108534529 | Common:8; Rare:133 | ||||
chr2:111884178-111884247 | Rare:14 | ||||
chr2:112645711-112645957 | Common:1; Rare:93 | ||||
chr2:113627078-113627272 | Common:1; Rare:54 | ||||
chr2:113756499-113756732 | Common:2; Rare:71 | ||||
chr2:118014071-118014236 | Common:2; Rare:92 |