Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23034883-23035209 | Common:2; Rare:68 | ||||
chr14:23095099-23095219 | Rare:58 | ||||
chr14:23095434-23095567 | Common:2; Rare:52 | ||||
chr14:23306639-23306890 | Common:1; Rare:55 | ||||
chr14:23953661-23953810 | Common:6; Rare:53 | ||||
chr14:23988766-23988930 | Common:8; Rare:66 | ||||
chr14:24114943-24115325 | Common:2; Rare:112 | ||||
chr14:24146564-24146881 | Common:1; Rare:100 | ||||
chr14:24195417-24195729 | Common:1; Rare:72 | ||||
chr14:24232330-24232677 | Common:8; Rare:80 | ||||
chr14:24242589-24242770 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24299714-24299863 | Common:4; Rare:42 | ||||
chr14:24429852-24429942 | Rare:23 | ||||
chr14:24442670-24443023 | Common:5; Rare:114 | ||||
chr14:31025558-31025664 | Common:1; Rare:25 |