Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40647758-40648173 | Rare:106 | ||||
chr17:40648178-40648430 | Common:2; Rare:54 | ||||
chr17:40818746-40818890 | Rare:66 | ||||
chr17:40818929-40819201 | Common:8; Rare:178; Clinvar (benign):1 | ||||
chr17:41688438-41689005 | Common:3; Rare:198 | ||||
chr17:41689176-41689618 | Common:4; Rare:163 | ||||
chr17:41836141-41836339 | Common:1; Rare:52 | ||||
chr17:41864679-41865027 | Rare:74 | ||||
chr17:41865113-41865157 | Rare:9 | ||||
chr17:41865273-41865630 | Common:2; Rare:158 | ||||
chr17:41918728-41918835 | Common:1; Rare:18 | ||||
chr17:41918881-41919377 | Common:3; Rare:169; Clinvar:1 | ||||
chr17:41930447-41930661 | Rare:57 | ||||
chr17:41966527-41967011 | Common:3; Rare:139 | ||||
chr17:42017114-42017779 | Common:1; Rare:200 |