chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X116116812116116813TC19GENICpossibly homozygous45200738
X116118098116118099CA12GENIChomozygous45920911
X116118182116118183C-5GENIChomozygous45200741
X116118185116118186CA5GENIChomozygous45481662
X116118194116118195AC4GENIChomozygous45200742
X116118354116118355CCG5GENIChomozygous45200743
X116118391116118392GA4GENIChomozygous45920913
X116118527116118535TGTATGTA--------5GENIChomozygous45200744
X116119911116119912AG15GENICheterozygous45920914
X116120476116120477GA13GENICpossibly homozygous45200750
X116120697116120698CT22GENIChomozygous45200751