chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171074144410741445TC22GENIChomozygous805078933
171074150210741503AG22GENIChomozygous805078934
171074226910742270AG23GENIChomozygous805078935
171074261310742614CT22GENIChomozygous805078936
171074354810743549AT15GENIChomozygous805078937
171074386110743862CT14GENIChomozygous805078938
171074394610743947AG13GENIChomozygous805078939
171074469410744695TG20GENIChomozygous805078940
171074484410744845TA28GENIChomozygous805078941
171074578110745782TG25GENIChomozygous805078942
171074603910746040GC41GENIChomozygous805078943
171074604710746048GA38GENIChomozygous805078944
171076068010760681TC25GENIChomozygous805078945
171076127510761276AT25GENIChomozygous805078946
171076760610767607CG24GENICheterozygous805078947
171076841910768420CG31GENIChomozygous805078948
171076918710769188TG19GENICpossibly homozygous805078949