chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
158370423883704239TC24GENIChomozygous813952930
158370434983704350CT20GENIChomozygous813952931
158370601583706016TA11GENICpossibly homozygous813952932
158370721983707220AC19GENIChomozygous813952933
158370731383707314CT20GENIChomozygous813952934
158370866283708663TC31GENIChomozygous813952935
158370871483708715TC22GENIChomozygous813952936
158370942583709426AG21GENIChomozygous813952937
158370942883709429GA22GENIChomozygous813952938
158370959983709600AG43GENIChomozygous813952939
158370992883709929GT21GENIChomozygous813952940
158371185883711859AG34GENIChomozygous813952941
158371256583712566GA22GENIChomozygous813952942
158371477883714779AT13GENIChomozygous813952943
158371481283714813TC12GENIChomozygous813952944
158371491183714912CT29GENIChomozygous813952945
158371504483715045CT18GENIChomozygous813952946
158371524283715243GA21GENIChomozygous813952947
158371535783715358AC38GENIChomozygous813952948
158371586483715865TG23GENIChomozygous813952949
158371625083716251GA19GENIChomozygous813952950
158371630683716307AG18GENIChomozygous813952951
158371675383716754GA11GENIChomozygous813952952
158371752083717521CT38GENIChomozygous813952953
158371785483717855TG18GENIChomozygous813952954
158371803383718034AC23GENIChomozygous813952955
158371865583718656TC18GENIChomozygous813952956
158371869983718700GA22GENIChomozygous813952957
158371926783719268CG30GENIChomozygous813952958
158372029983720300TC27GENIChomozygous813952959
158372106183721062GA36GENIChomozygous813952960
158372184983721850GA17GENIChomozygous813952961