chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124069553740695538AG13GENIChomozygous776835061
124069585940695860GA33GENIChomozygous776835062
124069586340695864CT35GENIChomozygous776835063
124069613340696134CA53GENIChomozygous776835064
124069615140696152GA54GENIChomozygous776835065
124069621640696217TC48GENIChomozygous776835066
124069664840696649AT12GENIChomozygous776835067
124069688440696885AT21GENIChomozygous776835068
124069744640697447TC43GENIChomozygous776835069
124069746740697468CT46GENIChomozygous776835070
124069805540698056GA25GENICpossibly homozygous776835071
124069956440699565CA45GENIChomozygous776835072
124069961840699619TC42GENIChomozygous776835073
124070027840700279GT53GENIChomozygous776835074
124070058640700587TC24GENIChomozygous776835075
124070065240700653CG11GENIChomozygous776835076
124070131740701318CA24GENIChomozygous776835077
124070156340701564GA46GENIChomozygous776835078
124070532540705326AG46GENIChomozygous776835079