chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,101040692,101040693,T,TACCTCTTGAGGGGGTGA,1,GENIC,homozygous,60779696 1,101040759,101040760,C,-,10,GENIC,homozygous,60779697 1,101040798,101040802,CCAA,----,2,GENIC,homozygous,60779698