chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35574943155749433AG--8GENIChomozygous57378647
35574958655749587CCAG7GENIChomozygous57378649
35574990155749902GT13GENICheterozygous57378650
35575027155750272GA14GENIChomozygous57378652
35575062355750624AC9GENIChomozygous58361130
35575170255751703G-8GENIChomozygous58361132
35575195355751954TG6GENICheterozygous57378655
35575196955751970GA7GENIChomozygous57378657
35575210655752107AG8GENICheterozygous57378658
35575234855752349CG7GENIChomozygous57378662
35575246655752467AC12GENIChomozygous57378664
35575249255752493GA10GENICpossibly homozygous58361134
35575262655752627CT9GENICpossibly homozygous57378665
35575270555752706AT3GENICheterozygous57378669
35575272155752722TA4GENIChomozygous57378671
35575272355752724TA2GENIChomozygous57378672
35575299255752993CT3GENICheterozygous57378674
35575301655753017CA1GENIChomozygous57378676
35575303655753037GT1GENIChomozygous57378678
35575320355753204AC6GENICheterozygous57378681
35575398455753985GA1GENIChomozygous57378688
35575416755754168T-7GENIChomozygous57378690
35575449555754496TG10GENIChomozygous57378693
35575456055754561GA15GENIChomozygous58361138
35575482355754824GA6GENIChomozygous57378696
35575485555754856AG13GENICheterozygous57378698
35575488355754884AG19GENICpossibly homozygous57378699
35575490855754909AC23GENICpossibly homozygous57378701
35575582355755824TC10GENIChomozygous57378705
35575597155755972AG10GENIChomozygous57378707
35575658855756589TC12GENIChomozygous57378710
35575660755756608TA15GENIChomozygous57378712
35575753955757540CT19GENICpossibly homozygous58361144
35575766955757673AAGT----5GENIChomozygous58361146
35575831855758319TA23GENIChomozygous57378715
35575908355759084AC13GENIChomozygous57378717