chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117900759279007593GT17GENIChomozygous67084535
117901097979010980CT24GENICpossibly homozygous67084536
117901479879014799CG29GENIChomozygous67084537
117901540179015402GA26GENIChomozygous67084538
117901808579018086GC38GENIChomozygous67084539
117901869579018696CT21GENIChomozygous67084543
117901956179019562TG34GENICpossibly homozygous67084544
117901956579019566TA33GENICpossibly homozygous67084545
117902047779020478CT18GENIChomozygous67084546
117902743879027439TG17GENIChomozygous67084547
117902748479027485TC18GENICpossibly homozygous67084549
117902821879028219CT33GENICpossibly homozygous67084551
117902845979028460TC20GENIChomozygous67084553
117902896279028963CA30GENIChomozygous67084555
117902900379029004CT23GENIChomozygous67084557
117902949379029494TC25GENIChomozygous67084559
117903050179030502GA18GENIChomozygous67084561