chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
158370423883704239TC16GENIChomozygous983509692
158370434983704350CT20GENIChomozygous983509693
158370601583706016TA15GENIChomozygous983509694
158370673783706738CT18GENICheterozygous983509695
158370721983707220AC18GENIChomozygous983509696
158370731383707314CT5GENIChomozygous983509697
158370866283708663TC8GENIChomozygous983509698
158370871483708715TC11GENIChomozygous983509699
158370942583709426AG18GENIChomozygous983509700
158370942883709429GA17GENIChomozygous983509701
158370959983709600AG14GENIChomozygous983509702
158370992883709929GT18GENIChomozygous983509703
158371185883711859AG11GENIChomozygous983509704
158371256583712566GA19GENIChomozygous983509705
158371477883714779AT16GENIChomozygous983509706
158371481283714813TC15GENIChomozygous983509707
158371491183714912CT19GENIChomozygous983509708
158371504483715045CT22GENIChomozygous983509709
158371524283715243GA26GENIChomozygous983509710
158371535783715358AC25GENIChomozygous983509711
158371586483715865TG24GENIChomozygous983509712
158371625083716251GA21GENIChomozygous983509713
158371630683716307AG23GENIChomozygous983509714
158371675383716754GA21GENIChomozygous983509715
158371752083717521CT20GENIChomozygous983509716
158371785483717855TG19GENIChomozygous983509717
158371803383718034AC20GENIChomozygous983509718
158371865583718656TC26GENIChomozygous983509719
158371869983718700GA27GENIChomozygous983509720
158371926783719268CG17GENIChomozygous983509721
158372029983720300TC20GENIChomozygous983509722
158372106183721062GA13GENIChomozygous983509723