chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108631468986314690CT39GENIChomozygous776554717
108631488886314889AG62GENIChomozygous776554718
108631736686317367GT34GENIChomozygous776554719
108632007386320074GT36GENIChomozygous776554720
108632117686321177AG40GENIChomozygous776554721
108632166286321663GA47GENIChomozygous776554722
108632189886321899TC56GENICpossibly homozygous776554723
108632223486322235CT38GENICpossibly homozygous776554724
108632233386322334AG33GENIChomozygous776554725
108632860886328609TG23GENICheterozygous776554726
108632953486329535GA36GENICpossibly homozygous776554727
108633105086331051AG46GENIChomozygous776554728
108633212886332129CT48GENIChomozygous776554729
108633257886332579GT48GENIChomozygous776554730
108633562086335621CT57GENIChomozygous776554731