Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96208305-96208459 | Rare:72 | ||||
chr2:96208816-96208954 | Common:3; Rare:49 | ||||
chr2:96265964-96266290 | Common:2; Rare:98; Clinvar:1 | ||||
chr2:96816153-96816266 | Common:1; Rare:37 | ||||
chr2:97663997-97664294 | Rare:85 | ||||
chr2:98608416-98608637 | Common:1; Rare:95; Clinvar (benign):1 | ||||
chr2:99154918-99155041 | Common:1; Rare:51; Clinvar (benign):2 | ||||
chr2:99180985-99181226 | Common:2; Rare:71 | ||||
chr2:101252647-101252929 | Common:5; Rare:97 | ||||
chr2:108534204-108534471 | Common:7; Rare:112 | ||||
chr2:112584377-112584633 | Common:1; Rare:69 | ||||
chr2:112645675-112645942 | Common:2; Rare:94 | ||||
chr2:113627078-113627282 | Common:1; Rare:58 | ||||
chr2:118013785-118013913 | Common:1; Rare:40 | ||||
chr2:118014062-118014206 | Common:2; Rare:88 |