chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4537940545379406AAT18GENIChomozygous45127646
X4537951445379515C-20GENIChomozygous45127647
X4537951945379520AAG19GENIChomozygous45127648
X4539741245397414AC--13GENICheterozygous45507817
X4540643245406436TATC----15GENIChomozygous45587161
X4540962345409628ACTAG-----25GENICpossibly homozygous45587163
X4541779045417791AAAGCACT34GENIChomozygous45507821
X4541779345417794AACC35GENIChomozygous45507823
X4541779545417796AACT35GENIChomozygous45507825
X4541781145417812CCTATA34GENIChomozygous45127659
X4541814445418145CCCAG23GENIChomozygous45127660
X4541846545418466GGAAGA11GENIChomozygous45587165
X4541867545418676G-8GENICheterozygous45587167