chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9121456867121456868GT37GENICheterozygous117450573
9121456920121456921TC44GENICheterozygous117450577
9121456989121456990CT40GENICheterozygous117450579
9121457010121457011GA35GENICheterozygous117450581
9121457039121457040CT34GENICheterozygous117450583
9121457186121457187TG27GENICheterozygous117450585
9121457200121457201TG26GENICheterozygous117450587
9121457949121457950TC14GENICpossibly homozygous117450593
9121457983121457984CT15GENIChomozygous117641162