chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4148612732148612733CA16GENIChomozygous112876991
4148612901148612902GT21GENIChomozygous112876999
4148614034148614035CG24GENIChomozygous112877012
4148614068148614069TA23GENIChomozygous112877014
4148614086148614087GA22GENIChomozygous112877016
4148614103148614104AT27GENIChomozygous119281812
4148614104148614105TA28GENIChomozygous119281814
4148614171148614172CA32GENIChomozygous112877018
4148614277148614278TG30GENIChomozygous112877020
4148614300148614301GA23GENIChomozygous112877022
4148614320148614321GC23GENIChomozygous112877024
4148614327148614328CT23GENIChomozygous112877025
4148614440148614441GA35GENIChomozygous112877027
4148614525148614526GA30GENIChomozygous112877029
4148614583148614584AG31GENIChomozygous112877031
4148614691148614692TC34GENIChomozygous112877033
4148614703148614704AT42GENIChomozygous112877035
4148615091148615092CT17GENIChomozygous112877037
4148615273148615274TC34GENIChomozygous112877039
4148615276148615277GA33GENIChomozygous112877041
4148615365148615366TC23GENIChomozygous112877042
4148617733148617734AG31GENIChomozygous112877089