chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4537940545379406AAT9GENIChomozygous45127646
X4537951445379515C-14GENIChomozygous45127647
X4537951945379520AAG14GENIChomozygous45127648
X4540054845400549CCT5GENICheterozygous45335525
X4540643145406432TTTATC9GENIChomozygous45294407
X4540962445409628CTAG----15GENICpossibly homozygous45127657
X4539741245397414AC--14GENICheterozygous45507817
X4541701245417014AC--20GENICheterozygous45507819
X4541779045417791AAAGCACT15GENIChomozygous45507821
X4541779345417794AACC15GENIChomozygous45507823
X4541779545417796AACT15GENIChomozygous45507825
X4541781145417812CCTATA17GENIChomozygous45127659
X4541814445418145CCCAG13GENIChomozygous45127660
X4541867545418676G-1GENIChomozygous45587167