Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:34757290-34757552 | Common:1; Rare:73 | ||||
chr6:35259416-35259749 | Common:3; Rare:103 | ||||
chr6:35921047-35921212 | Common:1; Rare:76 | ||||
chr6:36874792-36874882 | Rare:31 | ||||
chr6:41921085-41921213 | Common:1; Rare:33 | ||||
chr6:42929235-42929562 | Common:3; Rare:91 | ||||
chr6:43013884-43014295 | Common:2; Rare:90 | ||||
chr6:43059808-43059913 | Rare:34 | ||||
chr6:43171416-43171524 | Rare:31 | ||||
chr6:43516840-43517133 | Common:5; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
chr6:43576024-43576164 | Rare:43; Clinvar:3 | ||||
chr6:43770620-43770778 | Rare:42 | ||||
chr6:43778069-43778214 | Rare:22 | ||||
chr6:44127334-44127675 | Common:4; Rare:99 | ||||
chr6:45422178-45422281 | Rare:22 |