Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:124539040-124539204 | Common:2; Rare:90; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:125091707-125091914 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
chr8:126558373-126558628 | Common:1; Rare:95 | ||||
chr8:127735873-127736076 | Rare:42 | ||||
chr8:127736109-127736269 | Common:3; Rare:32 | ||||
chr8:129939748-129940037 | Common:1; Rare:99 | ||||
chr8:134713025-134713151 | Common:1; Rare:44 | ||||
chr8:140511152-140511511 | Common:3; Rare:130 | ||||
chr8:141001202-141001488 | Common:3; Rare:105 | ||||
chr8:143018432-143018559 | Common:1; Rare:36 | ||||
chr8:143541430-143541623 | Common:2; Rare:67 | ||||
chr8:143597093-143597219 | Common:1; Rare:44 | ||||
chr8:143617458-143617844 | Common:4; Rare:147 | ||||
chr8:143829039-143829155 | Rare:42 | ||||
chr8:143829306-143829478 | Rare:64 |