chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64526660645266607GA42GENIChomozygous137762943
64526697045266971CT34GENIChomozygous137762944
64526728145267282GA49GENIChomozygous137762945
64526741545267416TC40GENIChomozygous137762946
64526812345268124TC52GENIChomozygous137762947
64526853945268540CA39GENIChomozygous137762948
64526884545268846TC53GENIChomozygous137762949
64526888345268884GA59GENIChomozygous137762950
64526895145268952AG60GENIChomozygous137762951
64526957045269571TC41GENIChomozygous137762952
64526976545269766TC52GENIChomozygous137762953
64527057545270576GT53GENIChomozygous137762954
64527058345270584CG51GENIChomozygous137762955
64526970345269703AATATC55GENIChomozygous137679925
64527042045270420TA44GENICpossibly homozygous137679926