chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,106314423,106314424,G,,8,GENIC,homozygous,140591235 X,106315571,106315572,T,C,8,GENIC,heterozygous,147425007 X,106359174,106359177,CTT,,3,GENIC,heterozygous,147422916 X,106366816,106366816,,TCTA,6,GENIC,homozygous,142745654