Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:22819740-22819902 | Common:3; Rare:30; Clinvar (benign):1 | ||||
chr14:22829741-22829915 | Rare:52 | ||||
chr14:22836330-22836767 | Common:5; Rare:103 | ||||
chr14:22871651-22872272 | Common:2; Rare:155 | ||||
chr14:22919029-22919420 | Common:8; Rare:106 | ||||
chr14:22929310-22929646 | Common:1; Rare:99 | ||||
chr14:22981754-22981907 | Rare:30 | ||||
chr14:22982494-22982932 | Common:4; Rare:156 | ||||
chr14:23007138-23007354 | Common:3; Rare:60 | ||||
chr14:23034801-23035209 | Common:3; Rare:101 | ||||
chr14:23071513-23071886 | Common:1; Rare:106 | ||||
chr14:23094883-23094923 | Rare:10 | ||||
chr14:23094968-23095617 | Common:3; Rare:253 | ||||
chr14:23154275-23154566 | Common:4; Rare:67 | ||||
chr14:23155250-23155494 | Common:2; Rare:63 |