chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124688028946880290TC22GENIChomozygous115511796
124688345246883453GC12GENIChomozygous115342657
124688365146883652TC7GENIChomozygous115397205
124688461746884618GA28GENIChomozygous115511797
124688756646887567CT18GENIChomozygous115511798
124688908046889081GT23GENIChomozygous115397211
124688911646889117GA23GENICpossibly homozygous115397213
124688929246889293TC18GENIChomozygous115342671
124688967746889678GA18GENIChomozygous115342673