Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:54902819-54902976 | Rare:44; Clinvar (benign):1 | ||||
chr14:55027048-55027290 | Common:2; Rare:69 | ||||
chr14:55051473-55051749 | Rare:122 | ||||
chr14:55128489-55128777 | Common:4; Rare:55 | ||||
chr14:55129055-55129298 | Common:1; Rare:59 | ||||
chr14:55191553-55191756 | Common:4; Rare:47 | ||||
chr14:55271270-55271480 | Common:2; Rare:73 | ||||
chr14:55271975-55272039 | Common:1; Rare:13 | ||||
chr14:55272054-55272195 | Common:1; Rare:35 | ||||
chr14:55411727-55411878 | Rare:78 | ||||
chr14:55580096-55580326 | Common:2; Rare:100 | ||||
chr14:56117871-56117930 | Common:1; Rare:8 | ||||
chr14:57268526-57268614 | Rare:23 | ||||
chr14:57268812-57269130 | Common:2; Rare:96 | ||||
chr14:57390388-57390685 | Common:1; Rare:86 |