chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4537940545379406AAT18GENIChomozygous45127646
X4537951445379515C-11GENIChomozygous45127647
X4537951945379520AAG11GENIChomozygous45127648
X4539741245397414AC--5GENICheterozygous45507817
X4540643145406432TTTATC1GENIChomozygous45294407
X4540962445409628CTAG----9GENICpossibly homozygous45127657
X4541779045417791AAAGCACT18GENIChomozygous45507821
X4541779345417794AACC19GENIChomozygous45507823
X4541779545417796AACT18GENIChomozygous45507825
X4541781145417812CCTATA15GENIChomozygous45127659
X4541814445418145CCCAG21GENIChomozygous45127660