Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40318082-40318306 | Common:1; Rare:48 | ||||
chr17:40342038-40342403 | Common:1; Rare:80 | ||||
chr17:40417914-40418216 | Rare:102 | ||||
chr17:40443787-40444084 | Common:2; Rare:65 | ||||
chr17:41688631-41688922 | Common:1; Rare:103 | ||||
chr17:41772734-41772913 | Common:2; Rare:22 | ||||
chr17:41966606-41966882 | Common:1; Rare:99 | ||||
chr17:42017382-42017517 | Common:1; Rare:56 | ||||
chr17:42017531-42017636 | Rare:34 | ||||
chr17:42017640-42017665 | Rare:5 | ||||
chr17:42458751-42458956 | Common:3; Rare:77 | ||||
chr17:42566940-42567159 | Common:3; Rare:77 | ||||
chr17:42577671-42577844 | Rare:85 | ||||
chr17:42609326-42609732 | Common:8; Rare:172; Clinvar (benign):2 | ||||
chr17:42760960-42761263 | Rare:77 |