chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139477850139477851CT22GENIChomozygous114028836
5139479020139479021AG20GENIChomozygous114028838
5139479183139479184GA23GENIChomozygous114028839
5139480290139480291GT20GENIChomozygous114028840
5139481122139481123GC26GENIChomozygous114028841
5139483420139483421CG26GENIChomozygous114028842
5139489926139489927AG10GENIChomozygous114028843
5139491776139491777GA26GENIChomozygous114028844
5139494618139494619AG15GENIChomozygous114028845
5139496389139496390TC24GENIChomozygous114028847
5139496695139496696TA19GENIChomozygous114028848
5139502271139502272TG14GENIChomozygous114028850
5139502895139502896TC20GENIChomozygous114028851
5139503824139503825GT25GENICpossibly homozygous114028854
5139503903139503904AG15GENIChomozygous114028855
5139504040139504041CT12GENIChomozygous114028856
5139504610139504611AG2GENIChomozygous114028857