chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101367260513672606GA27GENICpossibly homozygous51621900
101367304713673048TC13GENIChomozygous51621901
101367329513673296C-4GENIChomozygous51621902
101367331013673311AC6GENICheterozygous51621903
101367441913674420GGAAAAAAAAAAAA1GENIChomozygous52313013
101367442213674423GGAAGA1GENIChomozygous52313014
101367501313675014CT16GENIChomozygous51621905
101367608113676082AG13GENIChomozygous51621909
101367621213676213CT11GENIChomozygous51621910
101367685713676858CT25GENIChomozygous51621912
101367705113677052TC12GENIChomozygous51621913
101367728813677289AC14GENICpossibly homozygous51621914
101368027813680279GA29GENICpossibly homozygous51621917
101368047813680479GGCA8GENICheterozygous51621918
101368066013680662AA--3GENICheterozygous51621919
101368090513680906AC10GENICpossibly homozygous51621922
101368145813681459GA15GENICheterozygous51621923
101368251313682514GA17GENICpossibly homozygous51621924
101368284813682849GA16GENICpossibly homozygous51621925
101368292813682929CT13GENICpossibly homozygous51621926
101368293513682936TG13GENIChomozygous51621927
101368316413683165GA22GENICpossibly homozygous51621928
101368431513684316GA21GENIChomozygous51621929
101368480813684809AG9GENIChomozygous51621930
101368759313687594CT7GENICpossibly homozygous51621931