chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	166031601	166031602	C	T	32	GENIC	homozygous	108355978
1	166031632	166031633	C	T	37	GENIC	homozygous	108355979
1	166031659	166031660	A	G	38	GENIC	homozygous	108355980
1	166032837	166032838	T	G	42	GENIC	homozygous	108355981
1	166033538	166033539	C	T	46	GENIC	homozygous	108355982
1	166033956	166033957	T	C	41	GENIC	homozygous	108355983
1	166034463	166034464	A	G	51	GENIC	homozygous	108355984
1	166034474	166034475	G	A	49	GENIC	homozygous	108355985
1	166034841	166034842	G	A	33	GENIC	homozygous	108355986
1	166036771	166036772	T	C	39	GENIC	homozygous	108355987
1	166038099	166038100	T	C	57	GENIC	homozygous	108355988
1	166038102	166038103	A	G	57	GENIC	homozygous	108355989
1	166038566	166038567	C	T	49	GENIC	homozygous	108355990
1	166039394	166039395	T	C	69	GENIC	homozygous	108355991
1	166040885	166040886	A	G	27	GENIC	homozygous	108355992
1	166041069	166041070	A	G	63	GENIC	heterozygous	108355993
1	166041095	166041096	A	G	41	GENIC	homozygous	108355994
1	166041196	166041197	C	T	49	GENIC	homozygous	108355995
1	166041868	166041869	C	T	46	GENIC	homozygous	108355996
1	166043441	166043442	G	A	53	GENIC	homozygous	108355997
1	166043950	166043951	A	G	50	GENIC	homozygous	108355998
1	166044972	166044973	G	A	48	GENIC	homozygous	108355999