chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
196301898663018987GGTTTTTTTTT3GENIChomozygous46432673
196301900363019004GA10GENIChomozygous46183509
196301908463019085T-14GENIChomozygous46310841
196301909163019092TA14GENIChomozygous46432675
196301932163019322C-16GENIChomozygous46310842
196301966363019664GA43GENIChomozygous46310843
196302147663021477GT14GENIChomozygous46310844
196302237363022374TC16GENIChomozygous46310845
196302253163022532AG21GENIChomozygous46310846
196302287763022878GA31GENIChomozygous46310847
196302289063022891AC35GENIChomozygous46310848
196302351063023511AG24GENIChomozygous46310849
196302384063023841CCT29GENICpossibly homozygous46310850
196302462763024628AG26GENIChomozygous46310851
196302540563025406CT27GENIChomozygous46310852
196302592763025931CACA----4GENICheterozygous46432677
196302592963025931CA--4GENICheterozygous46432679
196302698663026987CT19GENIChomozygous46310854
196302722363027231GTGTGTGT--------6GENICheterozygous46432681
196302913963029140CG36GENIChomozygous46310855
196302977263029773T-8GENIChomozygous46310856
196302987963029880TC15GENIChomozygous46310857
196303001163030012TC14GENIChomozygous46310858
196303076863030769CT20GENIChomozygous46310859
196303088963030890CT21GENIChomozygous46310860