Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:36320580-36320727 | Common:3; Rare:52 | ||||
chr14:37197834-37198096 | Common:3; Rare:88 | ||||
chr14:39114092-39114356 | Common:2; Rare:85 | ||||
chr14:39170203-39170487 | Common:3; Rare:78 | ||||
chr14:39174890-39175291 | Common:6; Rare:139 | ||||
chr14:39267080-39267454 | Common:1; Rare:138 | ||||
chr14:39432431-39432618 | Common:6; Rare:60 | ||||
chr14:44961892-44962223 | Common:2; Rare:93 | ||||
chr14:45083924-45084166 | Common:1; Rare:95 | ||||
chr14:45253078-45253310 | Rare:61 | ||||
chr14:47626537-47626626 | Rare:39 | ||||
chr14:49586297-49586776 | Common:1; Rare:247; Clinvar (benign):1 | ||||
chr14:49598731-49599023 | Common:1; Rare:107 | ||||
chr14:49620567-49620837 | Common:2; Rare:112; Clinvar:3 | ||||
chr14:49688201-49688266 | Rare:22 |