chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X134747359134747360GA5GENIChomozygous108343928
X134748480134748481TC12GENIChomozygous108343930
X134750343134750344T8GENIChomozygous129793548
X134755060134755061T9GENIChomozygous129793549
X134755080134755080TTGTTGTT6GENIChomozygous129793550
X134758459134758459TT12GENIChomozygous129793551
X134758553134758554AG10GENIChomozygous108343932
X134763617134763617AGTC10GENIChomozygous129793552
X134764907134764908C6GENIChomozygous129793553
X134764945134764946TC3GENIChomozygous108343934
X134765006134765006AG3GENIChomozygous129793554
X134765039134765040CT6GENIChomozygous108343936
X134765668134765669AG10GENIChomozygous108343938
X134766822134766823AT14GENIChomozygous108343940
X134767028134767029CT6GENIChomozygous108343942
X134767137134767138AT12GENIChomozygous108343944
X134767719134767720CG12GENIChomozygous108343946
X134767833134767834TC13GENIChomozygous108343948
X134768386134768387AT8GENIChomozygous108343950
X134768439134768440GA9GENIChomozygous108343952
X134769129134769130AC10GENIChomozygous108343954
X134769577134769578TG17GENIChomozygous108343956
X134769837134769838CT14GENIChomozygous108343958
X134770294134770295CT12GENIChomozygous108343960
X134772820134772821CT9GENIChomozygous108343962
X134773500134773501AC8GENIChomozygous108343964
X134773887134773888TA11GENIChomozygous108343966
X134774474134774475TG13GENIChomozygous108343968
X134775199134775200CT12GENIChomozygous108343970
X134781529134781530GA7GENIChomozygous108343972
X134783449134783450AG12GENIChomozygous108343974
X134783505134783506AT12GENIChomozygous108343976
X134785533134785533G14GENIChomozygous129793555
X134785672134785672T15GENIChomozygous129793556
X134787042134787043GT10GENIChomozygous108343978
X134791863134791864AG6GENIChomozygous108343980
X134792476134792477GA13GENIChomozygous108343982
X134764983134764984GA4GENIChomozygous119954529
X134765033134765034TA6GENIChomozygous108428218
X134765034134765035TG5GENIChomozygous108509060