chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	106635970	106635971	C	T	36	GENIC	homozygous	112639929
15	106636511	106636512	G	T	39	GENIC	homozygous	112639931
15	106637769	106637770	G	C	39	GENIC	homozygous	112639933
15	106638713	106638714	C	T	29	GENIC	homozygous	112639935
15	106639478	106639479	C	T	51	GENIC	homozygous	112639937
15	106646082	106646083	G	A	32	GENIC	homozygous	112639939
15	106655995	106655996	C	T	48	GENIC	homozygous	112639941
15	106657331	106657332	G	A	45	GENIC	homozygous	112639943
15	106659090	106659091	G	T	32	GENIC	possibly homozygous	112639945
15	106666958	106666959	T	C	40	GENIC	homozygous	112639947
15	106669707	106669708	C	T	29	GENIC	homozygous	112639949
15	106670946	106670947	T	C	45	GENIC	homozygous	112639951
15	106672327	106672328	C	A	53	GENIC	homozygous	112639953
15	106673179	106673180	A	G	54	GENIC	homozygous	112639955