Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31132475-31132855 | Common:1; Rare:100 | ||||
chr16:47598996-47599221 | Rare:49 | ||||
chr16:53373380-53373521 | Rare:32 | ||||
chr16:56617365-56617516 | Common:3; Rare:31 | ||||
chr16:56991730-56992040 | Common:1; Rare:63 | ||||
chr16:57485146-57485353 | Rare:36 | ||||
chr16:66852186-66852464 | Rare:38 | ||||
chr16:66961884-66962198 | Rare:36 | ||||
chr16:67203086-67203343 | Common:1; Rare:92 | ||||
chr16:67429382-67429877 | Common:3; Rare:79 | ||||
chr16:67432215-67432481 | Rare:60 | ||||
chr16:67432558-67432573 | Rare:2 | ||||
chr16:67434206-67434426 | Rare:36 | ||||
chr16:67435603-67436141 | Common:3; Rare:157; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr16:67436142-67436385 | Rare:90; Clinvar (benign):1; Clinvar (pathogenic):3 |