Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:169162891-169163266 | Common:3; Rare:74 | ||||
chr7:44986602-44986766 | Common:2; Rare:83 | ||||
chr7:45768893-45769141 | Common:3; Rare:71 | ||||
chr7:66493551-66493751 | Common:3; Rare:81 | ||||
chr7:66654444-66654568 | Rare:47 | ||||
chr7:67302394-67302742 | Common:5; Rare:112 | ||||
chr7:73005867-73006152 | Rare:26 | ||||
chr7:74890542-74890823 | Common:2; Rare:86 | ||||
chr7:75358952-75359239 | Common:1; Rare:8 | ||||
chr7:94404552-94404890 | Rare:85; Clinvar:6; Clinvar (pathogenic):1 | ||||
chr7:94408180-94408380 | Common:1; Rare:55; Clinvar:3 | ||||
chr7:94409317-94409804 | Common:4; Rare:134; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr7:94420277-94420640 | Rare:103; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr7:100335846-100336146 | Common:1; Rare:100 | ||||
chr7:130912176-130912369 | Common:1; Rare:31 |