Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:27549897-27550161 | Common:2; Rare:93 | ||||
chr16:28846299-28846603 | Common:2; Rare:104; Clinvar:5; Clinvar (benign):3 | ||||
chr16:30075919-30076059 | Common:1; Rare:48 | ||||
chr16:30375840-30376219 | Rare:90 | ||||
chr16:46973632-46973755 | Rare:59 | ||||
chr16:47461052-47461343 | Common:2; Rare:97; Clinvar (benign):1 | ||||
chr16:53703836-53704179 | Rare:95; Clinvar:3 | ||||
chr16:56451327-56451573 | Common:1; Rare:66 | ||||
chr16:56625693-56625799 | Rare:29 | ||||
chr16:57186018-57186335 | Common:1; Rare:94 | ||||
chr16:57447364-57447514 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
chr16:58129311-58129567 | Common:2; Rare:80 | ||||
chr16:66934377-66934469 | Rare:36 | ||||
chr16:67226859-67227145 | Common:1; Rare:99 | ||||
chr16:67481145-67481380 | Common:1; Rare:74 |