Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:64504587-64504770 | Rare:50 | ||||
chr14:64942734-64942959 | Common:1; Rare:51 | ||||
chr14:64987097-64987255 | Rare:61 | ||||
chr14:65102365-65102804 | Common:9; Rare:122; Clinvar:3; Clinvar (benign):5 | ||||
chr14:65411734-65411937 | Common:2; Rare:57 | ||||
chr14:65412562-65412903 | Common:5; Rare:110 | ||||
chr14:66507811-66508216 | Rare:167 | ||||
chr14:66508401-66508555 | Rare:53; Clinvar (benign):1 | ||||
chr14:67241133-67241442 | Rare:76 | ||||
chr14:67359768-67360018 | Rare:79 | ||||
chr14:67360062-67360368 | Common:3; Rare:74 | ||||
chr14:67412123-67412245 | Rare:29 | ||||
chr14:67600199-67600333 | Common:4; Rare:55; Clinvar (pathogenic):1 | ||||
chr14:67674569-67674919 | Common:1; Rare:89 | ||||
chr14:67816578-67816797 | Common:1; Rare:38 |