chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157270729157270730TA23GENIChomozygous57533730
4157271167157271168GA8GENIChomozygous57533732
4157271541157271542CA23GENIChomozygous57533734
4157273359157273361AA--5GENIChomozygous57533736
4157273381157273382TG7GENIChomozygous57533738
4157273553157273565ACACACACACAC------------10GENICheterozygous58595501
4157273555157273565ACACACACAC----------10GENICheterozygous58445184
4157273879157273880GA12GENIChomozygous57533742
4157274135157274136CG14GENIChomozygous57533744
4157274416157274417GA16GENIChomozygous57533746
4157274820157274821TC17GENIChomozygous57533748
4157275477157275478GT18GENIChomozygous57533750
4157275873157275874TC25GENIChomozygous57533752
4157276089157276090CT13GENIChomozygous57533754
4157276354157276355AT25GENIChomozygous57533756
4157276887157276888AAAC11GENICheterozygous57533758
4157277027157277028TTACACACAC10GENIChomozygous58348851
4157277204157277205TC8GENIChomozygous57533764
4157277710157277711T-7GENIChomozygous57533766
4157278618157278620AT--5GENIChomozygous58348855
4157278621157278622TC5GENIChomozygous58348857
4157278686157278687AG14GENIChomozygous57533770
4157278715157278716AG12GENIChomozygous57533772
4157278878157278879AG12GENIChomozygous57533774
4157279072157279073TG9GENIChomozygous57533776
4157279566157279567GA38GENIChomozygous57533778
4157279885157279886AT18GENIChomozygous57533780
4157279901157279902TC14GENIChomozygous57533782
4157280375157280376GC19GENIChomozygous57533784
4157280419157280420AC18GENICpossibly homozygous57533786
4157280509157280510AT7GENIChomozygous57533788
4157276887157276888AAACAC11GENICheterozygous56996730