chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
132592959225929593GC31GENIChomozygous956020735
132593001425930015CG31GENIChomozygous956020736
132593209825932099AG28GENIChomozygous956020737
132593396825933969AG27GENIChomozygous956020738
132593470925934710GT20GENIChomozygous956020739
132593570825935709CT29GENIChomozygous956020740
132593592225935923GA22GENIChomozygous956020741
132593969025939691CT18GENIChomozygous956020742
132593998125939982CG10GENIChomozygous956020743
132594018025940181CA14GENIChomozygous956020744
132594036925940370GA16GENIChomozygous956020745
132594109525941096TC22GENIChomozygous956020746
132594119525941196CA21GENIChomozygous956020747
132594120825941209CT19GENIChomozygous956020748
132594173625941737AG38GENIChomozygous956020749
132594208425942085CT22GENICpossibly homozygous956020750
132594308125943082GA46GENIChomozygous956020751
132594554825945549CT30GENIChomozygous956020752
132594982425949825TA39GENIChomozygous956020753