chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,124635881,124635882,G,C,28,GENIC,homozygous,931006025 X,124636223,124636224,G,A,12,GENIC,homozygous,931006026 X,124642452,124642453,A,G,18,GENIC,homozygous,931006027 X,124643201,124643202,C,T,27,GENIC,homozygous,931006028 X,124644532,124644533,C,T,15,GENIC,homozygous,931006029 X,124644755,124644756,C,T,27,GENIC,homozygous,931006030 X,124648028,124648029,G,T,10,GENIC,homozygous,931006031 X,124648043,124648044,C,T,10,GENIC,homozygous,931006032 X,124648547,124648548,A,G,33,GENIC,homozygous,931006033 X,124648836,124648837,T,C,28,GENIC,homozygous,931006034 X,124651865,124651866,G,C,21,GENIC,homozygous,931006035 X,124651980,124651981,C,T,16,GENIC,homozygous,931006036