chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4719174647191747CT1GENIChomozygous45337094
X4719289847192899GT9GENIChomozygous45128253
X4719291047192911GA9GENICheterozygous45476968
X4719291147192912AG9GENICheterozygous45476970
X4719440647194407GA2GENIChomozygous45296961
X4720455947204560AC4GENICheterozygous45296966
X4720472347204724CT3GENIChomozygous45296967
X4720819047208191GA15GENIChomozygous45337101
X4721383647213837GA7GENIChomozygous45337102
X4721389447213895CT4GENICheterozygous45296970
X4721413047214131CCA2GENICheterozygous45255188
X4721426847214269CA1GENIChomozygous45337103
X4722111947221120AG14GENIChomozygous45296973
X4722261747222618CA12GENIChomozygous45337105
X4722274647222747AG13GENICheterozygous45296975
X4722309447223095CT14GENICpossibly homozygous45296976
X4722470047224701GGTGTT2GENICheterozygous45337106
X4722614347226144AC7GENIChomozygous45296980
X4722769147227692CCA4GENIChomozygous45337107
X4722788847227889AG1GENIChomozygous45296981
X4722790447227905A-1GENIChomozygous45296982
X4723004347230044CT11GENIChomozygous45337109
X4723155447231556AT--2GENICheterozygous45296987
X4723332547233326GA10GENICheterozygous45337112
X4723717247237173TC4GENIChomozygous45296990