Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:42929211-42929562 | Common:3; Rare:99 | ||||
chr6:42984312-42984619 | Rare:78 | ||||
chr6:43013869-43014280 | Common:2; Rare:90 | ||||
chr6:43059812-43059913 | Rare:34 | ||||
chr6:43076166-43076431 | Rare:85 | ||||
chr6:43516846-43517120 | Common:5; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43575952-43576197 | Rare:97; Clinvar:4 | ||||
chr6:43635794-43635893 | Common:1; Rare:28 | ||||
chr6:43687769-43687874 | Common:1; Rare:42 | ||||
chr6:43770087-43770230 | Common:2; Rare:43 | ||||
chr6:43771896-43771996 | Rare:20 | ||||
chr6:44127351-44127644 | Common:4; Rare:84 | ||||
chr6:44257480-44257633 | Rare:42 | ||||
chr6:45377864-45378189 | Common:2; Rare:113 | ||||
chr6:47477695-47477797 | Rare:31 |