chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X134747359134747360GA13GENIChomozygous108343928
X134748480134748481TC7GENIChomozygous108343930
X134750343134750344T8GENIChomozygous129793548
X134755060134755061T8GENIChomozygous129793549
X134758553134758554AG12GENIChomozygous108343932
X134764945134764946TC1GENIChomozygous108343934
X134765039134765040CT4GENIChomozygous108343936
X134765668134765669AG14GENIChomozygous108343938
X134766822134766823AT6GENIChomozygous108343940
X134767028134767029CT12GENIChomozygous108343942
X134767137134767138AT15GENIChomozygous108343944
X134767719134767720CG16GENIChomozygous108343946
X134767833134767834TC8GENIChomozygous108343948
X134768386134768387AT10GENIChomozygous108343950
X134768439134768440GA10GENIChomozygous108343952
X134769129134769130AC8GENIChomozygous108343954
X134769577134769578TG10GENIChomozygous108343956
X134769837134769838CT7GENIChomozygous108343958
X134770294134770295CT8GENIChomozygous108343960
X134772820134772821CT19GENIChomozygous108343962
X134773500134773501AC9GENIChomozygous108343964
X134773887134773888TA5GENIChomozygous108343966
X134774474134774475TG12GENIChomozygous108343968
X134775199134775200CT13GENIChomozygous108343970
X134781529134781530GA7GENIChomozygous108343972
X134783449134783450AG14GENIChomozygous108343974
X134783505134783506AT16GENIChomozygous108343976
X134787042134787043GT13GENIChomozygous108343978
X134791863134791864AG11GENIChomozygous108343980
X134792476134792477GA10GENIChomozygous108343982
X134785533134785533G7GENIChomozygous129793555
X134755080134755080TTGTTGTT8GENIChomozygous129793550
X134758459134758459TT5GENIChomozygous129793551
X134763617134763617AGTC8GENIChomozygous129793552
X134785672134785672T8GENIChomozygous129793556
X134765033134765034TA4GENIChomozygous108428218
X134765034134765035TG4GENIChomozygous108509060