Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:21945831-21946196 | Common:3; Rare:116 | ||||
chr7:22220158-22220359 | Common:2; Rare:33 | ||||
chr7:22726986-22727205 | Common:1; Rare:24 | ||||
chr7:23105678-23105819 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
chr7:23181921-23182088 | Rare:72 | ||||
chr7:23470333-23470543 | Rare:67 | ||||
chr7:23531958-23532085 | Common:1; Rare:50 | ||||
chr7:24980108-24980414 | Common:8; Rare:129 | ||||
chr7:25125235-25125571 | Rare:136; Clinvar:3 | ||||
chr7:26200564-26201008 | Common:2; Rare:212 | ||||
chr7:26201195-26201560 | Rare:144 | ||||
chr7:26201586-26201843 | Common:2; Rare:126 | ||||
chr7:26202104-26202429 | Rare:139 | ||||
chr7:26864486-26864852 | Common:3; Rare:106 | ||||
chr7:27095965-27096297 | Rare:86 |