chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4117255591117255592GA22GENIChomozygous996828109
4117257889117257890CA15GENIChomozygous996828110
4117258118117258119CT15GENIChomozygous996828111
4117260219117260220GA27GENIChomozygous996828112
4117261107117261108TC30GENIChomozygous996828113
4117263458117263459CT15GENIChomozygous996828114
4117264803117264804CA9GENIChomozygous996828115
4117264818117264819CA9GENIChomozygous996828116
4117265590117265591CA23GENIChomozygous996828117
4117266678117266679GA16GENIChomozygous996828118
4117271434117271435TC22GENIChomozygous996828119
4117272285117272286AG13GENIChomozygous996828120
4117274035117274036CG25GENIChomozygous996828121
4117275127117275128AC25GENIChomozygous996828122
4117277269117277270AG17GENIChomozygous996828123
4117277305117277306CT13GENIChomozygous996828124
4117277584117277585TC14GENIChomozygous996828125
4117278233117278234CT14GENIChomozygous996828126
4117279408117279409TC30GENIChomozygous996828127
4117281635117281636GT35GENIChomozygous996828128
4117282737117282738GA22GENIChomozygous996828129
4117283800117283801CT29GENIChomozygous996828130