chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	24918562	24918563	C	A	29	GENIC	possibly homozygous	46394049
18	24918562	24918563	C	G	29	GENIC	heterozygous	46831844
18	24921645	24921646	C	T	26	GENIC	homozygous	46394050
18	24921703	24921704	A	T	26	GENIC	homozygous	46394052
18	24921881	24921882	G	A	27	GENIC	homozygous	46394053
18	24921963	24921964	C	CTG	10	GENIC	homozygous	46394055
18	24922187	24922188	A	C	22	GENIC	homozygous	46394057
18	24922322	24922323	A	-	19	GENIC	homozygous	46394058
18	24922346	24922347	A	T	21	GENIC	homozygous	46394060
18	24922653	24922654	A	G	32	GENIC	homozygous	46394061
18	24926492	24926493	T	C	31	GENIC	homozygous	46394064
18	24926723	24926724	T	C	23	GENIC	homozygous	46394066
18	24928260	24928261	C	-	13	GENIC	homozygous	46394068