Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:39566306-39566441 | Common:1; Rare:66 | ||||
chr7:39623522-39623804 | Rare:90 | ||||
chr7:40134581-40134952 | Rare:113 | ||||
chr7:42932144-42932388 | Rare:91 | ||||
chr7:43869479-43869646 | Rare:48 | ||||
chr7:44044591-44044734 | Common:2; Rare:37 | ||||
chr7:44573891-44574062 | Common:3; Rare:48 | ||||
chr7:44582176-44582507 | Common:1; Rare:126 | ||||
chr7:44748369-44748577 | Rare:51 | ||||
chr7:44796389-44796769 | Common:3; Rare:151 | ||||
chr7:56051420-56051845 | Common:1; Rare:162; Clinvar:5; Clinvar (benign):1 | ||||
chr7:64563032-64563261 | Common:4; Rare:61 | ||||
chr7:66114750-66114908 | Common:1; Rare:74 | ||||
chr7:66115232-66115353 | Rare:25 | ||||
chr7:66996557-66996850 | Common:2; Rare:65 |