chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7191756	7191757	A		11	GENIC	heterozygous	403462927
20	7191756	7191757	A	C	11	GENIC	possibly homozygous	403462928
20	7191770	7191771	A		11	GENIC	heterozygous	403462929
20	7191770	7191771	A	C	11	GENIC	possibly homozygous	403462930
20	7191777	7191778	A		11	GENIC	heterozygous	403462931
20	7191777	7191778	A	C	11	GENIC	possibly homozygous	403462932