chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	97817655	97817656	T	C	26	GENIC	homozygous	66166266
13	97829013	97829014	T	G	12	GENIC	heterozygous	66641764
13	97829014	97829015	G	T	12	GENIC	heterozygous	66641767
13	97832442	97832443	C	G	23	GENIC	homozygous	66376195