Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:55491719-55491836 | Rare:29; Clinvar (pathogenic):1 | ||||
chr16:56991730-56992040 | Common:1; Rare:63 | ||||
chr16:57299918-57299953 | Common:4; Rare:26 | ||||
chr16:58421160-58421323 | Rare:37 | ||||
chr16:58450133-58450167 | Rare:9 | ||||
chr16:66725853-66726157 | Common:2; Rare:65 | ||||
chr16:72664947-72665133 | Common:1; Rare:52 | ||||
chr16:74368122-74368376 | Common:1; Rare:71 | ||||
chr16:81530380-81530693 | Common:1; Rare:82 | ||||
chr16:81539651-81539958 | Common:1; Rare:75 | ||||
chr16:88919223-88919336 | Common:3; Rare:35 | ||||
chr17:2399537-2399811 | Common:2; Rare:89 | ||||
chr17:2402053-2402273 | Common:1; Rare:78 | ||||
chr17:2405361-2405482 | Rare:21 | ||||
chr17:2563050-2563243 | Common:5; Rare:44 |