chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
196301898663018987GGTTTTTTTTT6GENIChomozygous46432673
196301900363019004GA9GENIChomozygous46183509
196301908463019085T-11GENIChomozygous46310841
196301909163019092TA11GENICpossibly homozygous46432675
196301932163019322C-11GENIChomozygous46310842
196301966363019664GA30GENIChomozygous46310843
196302147663021477GT27GENIChomozygous46310844
196302237363022374TC17GENIChomozygous46310845
196302253163022532AG28GENIChomozygous46310846
196302287763022878GA32GENIChomozygous46310847
196302289063022891AC29GENIChomozygous46310848
196302351063023511AG18GENIChomozygous46310849
196302384063023841CCT34GENICpossibly homozygous46310850
196302462763024628AG26GENIChomozygous46310851
196302540563025406CT24GENIChomozygous46310852
196302592563025931CACACA------2GENIChomozygous46446879
196302698663026987CT19GENIChomozygous46310854
196302722363027231GTGTGTGT--------10GENICheterozygous46432681
196302913963029140CG36GENIChomozygous46310855
196302977263029773T-7GENIChomozygous46310856
196302987963029880TC14GENIChomozygous46310857
196303001163030012TC21GENIChomozygous46310858
196303076863030769CT28GENIChomozygous46310859
196303088963030890CT26GENIChomozygous46310860