Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:32107482-32107515 | Rare:12 | ||||
chr12:32107525-32107555 | Rare:7 | ||||
chr12:32739793-32740054 | Common:2; Rare:73 | ||||
chr12:32755878-32756014 | Rare:45 | ||||
chr12:32896738-32896975 | Common:2; Rare:75; Clinvar:4; Clinvar (benign):5 | ||||
chr12:38905526-38905813 | Common:6; Rare:83 | ||||
chr12:38906282-38906559 | Common:2; Rare:59 | ||||
chr12:39619708-39620073 | Common:1; Rare:58 | ||||
chr12:40224811-40225095 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr12:41188691-41189103 | Common:4; Rare:162 | ||||
chr12:42238178-42238445 | Common:1; Rare:85 | ||||
chr12:42326021-42326215 | Common:1; Rare:64 | ||||
chr12:42483914-42484123 | Common:1; Rare:33 | ||||
chr12:43758753-43758995 | Common:2; Rare:68; Clinvar:2 | ||||
chr12:43806249-43806431 | Common:2; Rare:63 |