chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X134747359134747360GA10GENIChomozygous108343928
X134748480134748481TC7GENIChomozygous108343930
X134758553134758554AG6GENIChomozygous108343932
X134765033134765034TA9GENIChomozygous108428218
X134765034134765035TG9GENIChomozygous108509060
X134765668134765669AG10GENIChomozygous108343938
X134766822134766823AT7GENIChomozygous108343940
X134767028134767029CT5GENIChomozygous108343942
X134767137134767138AT13GENIChomozygous108343944
X134767719134767720CG8GENIChomozygous108343946
X134767833134767834TC9GENIChomozygous108343948
X134768386134768387AT8GENIChomozygous108343950
X134768439134768440GA14GENIChomozygous108343952
X134769129134769130AC7GENIChomozygous108343954
X134769577134769578TG7GENIChomozygous108343956
X134769837134769838CT7GENIChomozygous108343958
X134770294134770295CT11GENIChomozygous108343960
X134772820134772821CT4GENIChomozygous108343962
X134773500134773501AC6GENIChomozygous108343964
X134773887134773888TA10GENIChomozygous108343966
X134774474134774475TG16GENIChomozygous108343968
X134775199134775200CT4GENIChomozygous108343970
X134781529134781530GA8GENIChomozygous108343972
X134783449134783450AG11GENIChomozygous108343974
X134783505134783506AT9GENIChomozygous108343976
X134787042134787043GT17GENIChomozygous108343978
X134791863134791864AG8GENIChomozygous108343980
X134792476134792477GA11GENIChomozygous108343982