chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55949172159491722GA32GENIChomozygous807425730
55949242559492426AG43GENICpossibly homozygous807425731
55949358359493584GA30GENIChomozygous807425732
55949624259496243AG50GENIChomozygous807425733
55949794959497950GA47GENIChomozygous807425734
55950257959502580AC63GENICpossibly homozygous807425735
55950268359502684TC49GENIChomozygous807425736
55950269859502699AT50GENIChomozygous807425737
55950272059502721CT39GENIChomozygous807425738
55950296759502968CT40GENIChomozygous807425739
55950323259503233CT32GENIChomozygous807425740
55950324559503246CT26GENIChomozygous807425741
55950342259503423GA31GENICpossibly homozygous807425742
55950351459503515TC40GENIChomozygous807425743
55950411659504117TC29GENIChomozygous807425744
55950440659504407GA43GENIChomozygous807425745
55950448859504489AG36GENICpossibly homozygous807425746
55950488859504889TC39GENIChomozygous807425747
55950493459504935CT52GENIChomozygous807425748
55950546359505464TC71GENIChomozygous807425749
55950563159505632GC54GENIChomozygous807425750
55950888059508881TC43GENIChomozygous807425751