chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4719289847192899GT14GENICpossibly homozygous45128253
X4719291047192911GA11GENICheterozygous45476968
X4719291147192912AG13GENICheterozygous45476970
X4719440647194407GA1GENIChomozygous45296961
X4720455947204560AC2GENIChomozygous45296966
X4720472347204724CT3GENICheterozygous45296967
X4721389447213895CT5GENICheterozygous45296970
X4721413047214131CCA2GENICheterozygous45255188
X4722001947220020GA2GENIChomozygous45296972
X4722111947221120AG22GENICpossibly homozygous45296973
X4722274647222747AG19GENICpossibly homozygous45296975
X4722309447223095CT15GENIChomozygous45296976
X4722339747223401AACC----1GENIChomozygous45296977
X4722430747224308CT18GENIChomozygous45296978
X4722614347226144AC13GENIChomozygous45296980
X4723649947236500CT18GENICheterozygous45296989
X4723717247237173TC11GENIChomozygous45296990