Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:65411846-65411935 | Common:1; Rare:26 | ||||
chr14:65412569-65413039 | Common:5; Rare:144 | ||||
chr14:67359713-67360011 | Common:1; Rare:100 | ||||
chr14:67816580-67816729 | Rare:27 | ||||
chr14:69398306-69398723 | Common:2; Rare:105 | ||||
chr14:69611494-69611798 | Common:2; Rare:101 | ||||
chr14:70416973-70417149 | Rare:54 | ||||
chr14:73458481-73458903 | Common:6; Rare:116 | ||||
chr14:73463601-73463871 | Common:1; Rare:41 | ||||
chr14:73787172-73787355 | Common:2; Rare:70 | ||||
chr14:73950130-73950330 | Common:4; Rare:85; Clinvar (benign):2 | ||||
chr14:74019259-74019423 | Common:1; Rare:64 | ||||
chr14:74084403-74084637 | Common:2; Rare:60 | ||||
chr14:74493395-74493780 | Common:4; Rare:123; Clinvar (benign):4 | ||||
chr14:74494031-74494319 | Rare:106; Clinvar (benign):2 |