chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64526660645266607GA19GENIChomozygous137762943
64526697045266971CT15GENIChomozygous137762944
64526728145267282GA12GENIChomozygous137762945
64526741545267416TC25GENIChomozygous137762946
64526812345268124TC23GENIChomozygous137762947
64526853945268540CA29GENIChomozygous137762948
64526884545268846TC27GENIChomozygous137762949
64526888345268884GA22GENIChomozygous137762950
64526895145268952AG26GENIChomozygous137762951
64526957045269571TC30GENIChomozygous137762952
64526970345269703AATATC21GENIChomozygous137679925
64526976545269766TC19GENIChomozygous137762953
64527042045270420TA13GENICpossibly homozygous137679926
64527057545270576GT18GENIChomozygous137762954
64527058345270584CG18GENIChomozygous137762955