chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41028194010281941A9GENICheterozygous403578567
41028194010281941AT9GENICheterozygous403578568
41028194210281943A14GENICheterozygous403578569
41028194210281943AT14GENICheterozygous403578570
41028357010283571TC53GENIChomozygous136969701
41029540010295401TC55GENIChomozygous136969702
41031464010314641GT49GENIChomozygous136969703
41029606010296061T24GENICpossibly homozygous136866363