chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4148612732148612733CA21GENIChomozygous112876991
4148612778148612779AG26GENIChomozygous112876993
4148612901148612902GT26GENIChomozygous112876999
4148614034148614035CG26GENIChomozygous112877012
4148614068148614069TA23GENIChomozygous112877014
4148614086148614087GA20GENIChomozygous112877016
4148614103148614104AT25GENIChomozygous119281812
4148614104148614105TA25GENIChomozygous119281814
4148614171148614172CA29GENIChomozygous112877018
4148614277148614278TG34GENIChomozygous112877020
4148614300148614301GA35GENIChomozygous112877022
4148614320148614321GC34GENIChomozygous112877024
4148614327148614328CT36GENIChomozygous112877025
4148614440148614441GA32GENIChomozygous112877027
4148614525148614526GA29GENIChomozygous112877029
4148614583148614584AG21GENIChomozygous112877031
4148615273148615274TC19GENIChomozygous112877039
4148615276148615277GA19GENIChomozygous112877041
4148615365148615366TC22GENIChomozygous112877042
4148615402148615403CT14GENIChomozygous112877044
4148615799148615800AG29GENIChomozygous112877046