Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:20331719-20331885 | Common:1; Rare:62 | ||||
chr7:23105682-23105865 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
chr7:23181906-23182083 | Rare:75 | ||||
chr7:24980108-24980325 | Common:5; Rare:92 | ||||
chr7:26200640-26201008 | Common:2; Rare:180 | ||||
chr7:26201187-26201442 | Rare:103 | ||||
chr7:26201619-26201818 | Common:1; Rare:103 | ||||
chr7:27096020-27096198 | Rare:55 | ||||
chr7:27150935-27151038 | Rare:26 | ||||
chr7:27152571-27152738 | Rare:29 | ||||
chr7:27740022-27740223 | Common:5; Rare:68 | ||||
chr7:30504712-30505079 | Common:4; Rare:122 | ||||
chr7:30594717-30594996 | Common:4; Rare:133; Clinvar:6; Clinvar (benign):9 | ||||
chr7:32495247-32495564 | Rare:80 | ||||
chr7:35694868-35695270 | Common:4; Rare:113 |