chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71393940013939401TG18INTERGENIChomozygous53796660
71393967413939675CT16INTERGENIChomozygous53796661
71393974913939750T-17INTERGENICpossibly homozygous53796662
71393989113939892CT29INTERGENICpossibly homozygous53796663
71394034813940349TC14INTERGENIChomozygous53796664
71394041113940412TC12INTERGENICheterozygous53796665
71394059913940600AT15INTERGENIChomozygous53796666
71394065113940652CT15INTERGENIChomozygous53796667
71394086313940874GAGCAGTTAGT-----------2INTERGENIChomozygous53796669
71394103513941036GA10INTERGENICheterozygous53796670
71394172213941723TC21INTERGENIChomozygous53796671