chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71231887112318872TC20GENICpossibly homozygous115569807
71231895812318959TC31GENIChomozygous115569808
71231929612319297CT25GENICpossibly homozygous115569810
71231965712319658GA28GENICpossibly homozygous115569811
71231997212319973TC35GENIChomozygous115569812
71232013612320137CG17GENICpossibly homozygous115569813
71232102712321028TC28GENIChomozygous115569814
71232202812322029GA20GENIChomozygous118407622
71232284112322842GA29GENICpossibly homozygous115569815
71232296212322963CT37GENICpossibly homozygous115569816
71232337712323378TC40GENIChomozygous115569817
71232434012324341GC24GENIChomozygous118407623