chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	72105048	72105049	A	T	34	GENIC	possibly homozygous	46969233
18	72105141	72105142	G	A	34	GENIC	homozygous	46511513
18	72105492	72105493	T	C	35	GENIC	homozygous	46511514
18	72105886	72105887	C	-	16	GENIC	homozygous	46969234
18	72105895	72105896	C	T	17	GENIC	homozygous	46969235
18	72106101	72106102	T	C	15	GENIC	homozygous	46783868
18	72106366	72106367	G	C	19	GENIC	homozygous	46783869
18	72106500	72106501	C	CGCGTGCGT	18	GENIC	homozygous	46969236
18	72106601	72106602	G	C	19	GENIC	homozygous	46783870