chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 5,64789543,64789544,G,A,50,GENIC,homozygous,978995860 5,64790852,64790853,T,C,25,GENIC,homozygous,978995861 5,64791602,64791603,T,A,28,GENIC,homozygous,978995862 5,64793189,64793190,G,C,21,GENIC,homozygous,978995863 5,64794323,64794324,C,T,11,GENIC,homozygous,978995864 5,64794679,64794680,C,T,16,GENIC,homozygous,978995865 5,64794718,64794719,A,G,16,GENIC,homozygous,978995866 5,64795355,64795356,T,C,49,GENIC,homozygous,978995867 5,64795586,64795587,T,G,13,GENIC,homozygous,978995868 5,64795589,64795590,G,T,11,GENIC,homozygous,978995869 5,64795682,64795683,A,G,17,GENIC,homozygous,978995870 5,64795909,64795910,G,A,16,GENIC,homozygous,978995871 5,64796110,64796111,A,G,9,GENIC,homozygous,978995872 5,64796715,64796716,A,G,39,GENIC,homozygous,978995873 5,64796985,64796986,A,G,18,GENIC,homozygous,978995874 5,64799544,64799545,C,T,43,GENIC,homozygous,978995875 5,64799790,64799791,A,G,29,GENIC,homozygous,978995876 5,64800240,64800241,G,C,30,GENIC,homozygous,978995877