chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104540852945408530AG51GENIChomozygous138783866
104540894945408950CT71GENIChomozygous138783867
104540968145409682AG63GENIChomozygous138783868
104540977045409771AG66GENIChomozygous138783869
104541004945410050CT61GENIChomozygous138783870
104541125445411255GA59GENICpossibly homozygous138783871
104541239445412395CT69GENIChomozygous138783872
104541282945412830AG70GENIChomozygous138783873
104541306945413070GC65GENIChomozygous138783874
104541351845413519TG74GENIChomozygous138783875
104541373045413731CT77GENIChomozygous138783876