Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42388555-42388845 | Common:1; Rare:71 | ||||
chr17:42422988-42423310 | Common:1; Rare:103; Clinvar:3 | ||||
chr17:42458724-42458950 | Common:3; Rare:83 | ||||
chr17:42566901-42567127 | Common:3; Rare:78 | ||||
chr17:42577680-42577864 | Common:1; Rare:90 | ||||
chr17:42609316-42609743 | Common:8; Rare:180; Clinvar (benign):2 | ||||
chr17:42659333-42659543 | Rare:58 | ||||
chr17:42682423-42682574 | Rare:32 | ||||
chr17:42745023-42745172 | Common:3; Rare:54 | ||||
chr17:42760928-42761264 | Rare:84 | ||||
chr17:42780474-42780617 | Common:1; Rare:47 | ||||
chr17:42798685-42798787 | Rare:30 | ||||
chr17:42833378-42833487 | Rare:44 | ||||
chr17:42964405-42964534 | Rare:61 | ||||
chr17:42980394-42980571 | Common:1; Rare:53 |