chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4146973704146973705GA38GENIChomozygous112873811
4146974069146974070CT46GENIChomozygous112873813
4146974519146974520TG30GENIChomozygous112873814
4146974573146974574TA30GENIChomozygous112873815
4146977287146977288GA48GENIChomozygous113180143
4146978306146978307AT42GENICpossibly homozygous113394408
4146978563146978564CT51GENICpossibly homozygous112873816
4146980424146980425TC49GENIChomozygous112873825