Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:43771697-43772022 | Common:4; Rare:55 | ||||
chr6:44127366-44127665 | Common:4; Rare:87 | ||||
chr6:44219458-44219682 | Common:2; Rare:60 | ||||
chr6:44387576-44387747 | Common:2; Rare:50 | ||||
chr6:46129777-46130071 | Common:5; Rare:91 | ||||
chr6:46652718-46653013 | Rare:74 | ||||
chr6:47309635-47309764 | Rare:24 | ||||
chr6:47477676-47478248 | Common:5; Rare:170; Clinvar:7; Clinvar (benign):7 | ||||
chr6:49463225-49463383 | Common:1; Rare:47; Clinvar (benign):1 | ||||
chr6:52420122-52420364 | Common:3; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
chr6:52577349-52577462 | Common:1; Rare:37 | ||||
chr6:52995255-52995817 | Common:4; Rare:229 | ||||
chr6:53061725-53061916 | Rare:41 | ||||
chr6:54846439-54846809 | Common:2; Rare:90 | ||||
chr6:56542786-56543047 | Common:2; Rare:46 |