chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157268939157268947AGTGATCC--------6GENICheterozygous58348845
4157269675157269676CT24GENIChomozygous57960274
4157270199157270200TC27GENIChomozygous57960277
4157270307157270308CA14GENIChomozygous57960280
4157270729157270730TA26GENICpossibly homozygous57533730
4157270998157270999GT27GENIChomozygous57960283
4157271653157271654AT31GENIChomozygous57960286
4157273226157273227TA18GENIChomozygous57960292
4157273359157273361AA--15GENIChomozygous57533736
4157273381157273382TG18GENIChomozygous57533738
4157274416157274417GA22GENIChomozygous57533746
4157274468157274469AG28GENIChomozygous57960298
4157274820157274821TC28GENIChomozygous57533748
4157275477157275478GT35GENIChomozygous57533750
4157275873157275874TC38GENIChomozygous57533752
4157276060157276061GA32GENIChomozygous58673143
4157276089157276090CT29GENIChomozygous57533754
4157277027157277028TTACAC17GENICheterozygous57533762
4157277027157277028TTACACAC17GENICpossibly homozygous58348849
4157277398157277399GC27GENIChomozygous57960307
4157277710157277711T-14GENIChomozygous57533766
4157277762157277763CT12GENIChomozygous57960313
4157277941157277942TC11GENIChomozygous57960316
4157278148157278149GA26GENIChomozygous58673145
4157278592157278593CA11GENIChomozygous57960322
4157278615157278616AAAT3GENICheterozygous58673147
4157278615157278616AAATAT3GENICheterozygous59541172
4157278650157278651AG4GENIChomozygous57960325
4157278686157278687AG9GENIChomozygous57533770
4157279566157279567GA25GENIChomozygous57533778
4157279885157279886AT30GENIChomozygous57533780
4157279997157279998TG30GENIChomozygous57960328
4157280014157280015TC27GENIChomozygous57960331
4157280077157280078CT30GENIChomozygous58673149
4157280078157280079CT36GENIChomozygous58673151
4157280207157280208GA23GENIChomozygous57960334
4157276887157276888AAACACAC6GENICheterozygous58407906
4157276887157276888AAACAC6GENICheterozygous56996730