chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151886720151886721TG28GENICpossibly homozygous114353599
5151887425151887426AC33GENIChomozygous114353601
5151888161151888162AG33GENIChomozygous114353603
5151888604151888605CT25GENIChomozygous114542406
5151888880151888881TA29GENIChomozygous114353605
5151889343151889344CT24GENIChomozygous114353607
5151891056151891057GA34GENIChomozygous114353611
5151891895151891896CT39GENICpossibly homozygous114542408
5151894480151894481CT65GENICheterozygous114353613
5151894688151894689CT27GENICpossibly homozygous114542410
5151896120151896121CA37GENIChomozygous114542412
5151897556151897557AG33GENIChomozygous114353615
5151897730151897731CT41GENIChomozygous114542414
5151898728151898729GA38GENIChomozygous114542416