chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X134747359134747360GA4GENIChomozygous108343928
X134748480134748481TC7GENIChomozygous108343930
X134758553134758554AG7GENIChomozygous108343932
X134765668134765669AG5GENIChomozygous108343938
X134766822134766823AT12GENIChomozygous108343940
X134767028134767029CT12GENIChomozygous108343942
X134767137134767138AT20GENIChomozygous108343944
X134767719134767720CG12GENIChomozygous108343946
X134767833134767834TC12GENIChomozygous108343948
X134768386134768387AT9GENIChomozygous108343950
X134768439134768440GA16GENIChomozygous108343952
X134769129134769130AC11GENIChomozygous108343954
X134769577134769578TG8GENIChomozygous108343956
X134769837134769838CT9GENIChomozygous108343958
X134770294134770295CT16GENIChomozygous108343960
X134772820134772821CT10GENIChomozygous108343962
X134773500134773501AC14GENIChomozygous108343964
X134773887134773888TA9GENIChomozygous108343966
X134774474134774475TG9GENIChomozygous108343968
X134775199134775200CT7GENIChomozygous108343970
X134781529134781530GA5GENIChomozygous108343972
X134783449134783450AG8GENIChomozygous108343974
X134783505134783506AT8GENIChomozygous108343976
X134787042134787043GT14GENIChomozygous108343978
X134791863134791864AG13GENIChomozygous108343980
X134792476134792477GA10GENIChomozygous108343982