chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,124921936,124921937,G,A,8,GENIC,homozygous,977768912 X,124924447,124924448,A,G,11,GENIC,homozygous,977768913 X,124924960,124924961,T,C,20,GENIC,homozygous,977768914 X,124924974,124924975,C,G,16,GENIC,homozygous,977768915