chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71231887112318872TC13GENIChomozygous115569807
71231895812318959TC14GENIChomozygous115569808
71231918712319188CT19GENICpossibly homozygous115569809
71231929612319297CT20GENIChomozygous115569810
71231965712319658GA11GENIChomozygous115569811
71231997212319973TC17GENIChomozygous115569812
71232013612320137CG9GENIChomozygous115569813
71232102712321028TC11GENIChomozygous115569814
71232284112322842GA8GENIChomozygous115569815
71232296212322963CT17GENIChomozygous115569816
71232337712323378TC19GENIChomozygous115569817