chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104892677048926771GC62GENIChomozygous781469595
104892745648927457GT39GENIChomozygous781469596
104892751348927514AG41GENIChomozygous781469597
104892777748927778TC59GENIChomozygous781469598
104892806248928063AG70GENIChomozygous781469599
104892873048928731TA58GENIChomozygous781469600