chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71231887112318872TC68GENIChomozygous115569807
71231895812318959TC54GENICpossibly homozygous115569808
71231918712319188CT55GENICpossibly homozygous115569809
71231929612319297CT62GENICpossibly homozygous115569810
71231965712319658GA56GENICpossibly homozygous115569811
71231997212319973TC57GENIChomozygous115569812
71232013612320137CG73GENIChomozygous115569813
71232102712321028TC40GENIChomozygous115569814
71232284112322842GA33GENICpossibly homozygous115569815
71232296212322963CT55GENIChomozygous115569816
71232337712323378TC80GENIChomozygous115569817