Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40885239-40885382 | Common:1; Rare:25 | ||||
chr17:41315698-41315990 | Common:3; Rare:51 | ||||
chr17:41586841-41587105 | Common:1; Rare:63 | ||||
chr17:41689239-41689512 | Common:4; Rare:105 | ||||
chr17:41812617-41813029 | Common:3; Rare:92; Clinvar:5 | ||||
chr17:41966606-41966837 | Common:1; Rare:83 | ||||
chr17:42017382-42017580 | Common:1; Rare:74 | ||||
chr17:42154941-42155265 | Common:3; Rare:83 | ||||
chr17:42423062-42423453 | Common:1; Rare:110; Clinvar:2 | ||||
chr17:42458738-42458938 | Common:3; Rare:75 | ||||
chr17:42566980-42567126 | Common:3; Rare:44 | ||||
chr17:42577671-42577825 | Rare:72 | ||||
chr17:42609333-42609732 | Common:8; Rare:165; Clinvar (benign):2 | ||||
chr17:42760974-42761239 | Rare:66 | ||||
chr17:42798685-42798778 | Rare:25 |