Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41966606-41966837 | Common:1; Rare:83 | ||||
chr17:42017382-42017518 | Common:1; Rare:56 | ||||
chr17:42017571-42017670 | Rare:32 | ||||
chr17:42154930-42155208 | Common:3; Rare:72 | ||||
chr17:42458681-42458945 | Common:3; Rare:95 | ||||
chr17:42577671-42577834 | Rare:81 | ||||
chr17:42609306-42609732 | Common:8; Rare:179; Clinvar (benign):2 | ||||
chr17:42682430-42682548 | Rare:26 | ||||
chr17:42745023-42745171 | Common:3; Rare:53 | ||||
chr17:42773375-42773495 | Rare:38 | ||||
chr17:42833340-42833497 | Rare:59 | ||||
chr17:42964410-42964534 | Rare:60 | ||||
chr17:43125324-43125714 | Rare:98; Clinvar:3; Clinvar (benign):3 | ||||
chr17:43170303-43170557 | Common:3; Rare:49 | ||||
chr17:43171035-43171255 | Rare:69 |