chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116449672764496728TC14GENICheterozygous50802229
116449933864499339CA15GENIChomozygous51234614
116449954064499541GT12GENICpossibly homozygous51234616
116449959364499594GC20GENIChomozygous51234618
116449993964499940AG25GENICpossibly homozygous51234619
116450003664500037AG24GENIChomozygous51234621
116450095764500958AG1GENIChomozygous51234623
116450119264501193GA18INTERGENIChomozygous51234625
116450132864501329GT23INTERGENIChomozygous51234627
116450137064501371TC8INTERGENICpossibly homozygous51234629
116450178564501786AC19INTERGENIChomozygous51234631
116450190864501909TC6INTERGENIChomozygous51234632
116450193064501931T-13INTERGENIChomozygous51234634
116450197064501971CT13INTERGENIChomozygous51234636
116450279364502794TC16INTERGENICpossibly homozygous51234638
116450430164504302GA15INTERGENIChomozygous51234640
116450520764505208TC8INTERGENIChomozygous50802257
116450521464505215TC4INTERGENIChomozygous50802259
116450773864507739AG10INTERGENICpossibly homozygous51234642