chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	166031304	166031305	G	T	37	GENIC	homozygous	109163061
1	166031601	166031602	C	T	33	GENIC	homozygous	108355978
1	166031659	166031660	A	G	38	GENIC	possibly homozygous	108355980
1	166031777	166031778	G	A	31	GENIC	homozygous	109163063
1	166032837	166032838	T	G	39	GENIC	possibly homozygous	108355981
1	166033538	166033539	C	T	30	GENIC	homozygous	108355982
1	166033956	166033957	T	C	45	GENIC	homozygous	108355983
1	166034463	166034464	A	G	37	GENIC	homozygous	108355984
1	166034474	166034475	G	A	39	GENIC	possibly homozygous	108355985
1	166034841	166034842	G	A	49	GENIC	homozygous	108355986
1	166036771	166036772	T	C	37	GENIC	homozygous	108355987
1	166036918	166036919	C	T	42	GENIC	homozygous	109163065
1	166038099	166038100	T	C	44	GENIC	homozygous	108355988
1	166038102	166038103	A	G	42	GENIC	homozygous	108355989
1	166038566	166038567	C	T	39	GENIC	homozygous	108355990
1	166039394	166039395	T	C	43	GENIC	homozygous	108355991
1	166040885	166040886	A	G	30	GENIC	homozygous	108355992
1	166041095	166041096	A	G	38	GENIC	homozygous	108355994
1	166041196	166041197	C	T	54	GENIC	possibly homozygous	108355995
1	166043950	166043951	A	G	40	GENIC	homozygous	108355998
1	166044454	166044455	T	C	36	GENIC	homozygous	109163067