chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	75693525	75693526	G	T	44	GENIC	possibly homozygous	109501865
1	75694615	75694616	T	C	34	GENIC	homozygous	120867054
1	75695765	75695766	T	C	57	GENIC	homozygous	120867055
1	75695963	75695964	A	G	37	GENIC	homozygous	109501869
1	75696041	75696042	T	C	35	GENIC	homozygous	109501870
1	75696072	75696073	T	C	44	GENIC	homozygous	109501871
1	75695049	75695050	A	C	37	GENIC	homozygous	120886141
1	75696599	75696600	C	G	40	GENIC	homozygous	109501873
1	75697152	75697153	A	T	33	GENIC	homozygous	109501874
1	75697358	75697359	A	G	43	GENIC	homozygous	120867056
1	75697461	75697462	C	T	43	GENIC	homozygous	120867057
1	75697831	75697832	T	C	40	GENIC	homozygous	109501876
1	75698020	75698021	G	A	51	GENIC	homozygous	120867058
1	75698629	75698630	T	C	49	GENIC	homozygous	109501878
1	75699799	75699800	G	A	42	GENIC	homozygous	120867059
1	75701429	75701430	T	G	48	GENIC	homozygous	109501879
1	75701972	75701973	C	A	36	GENIC	homozygous	120867060
1	75703479	75703480	T	A	41	GENIC	homozygous	120867061
1	75703805	75703806	C	T	24	GENIC	homozygous	109501881
1	75704994	75704995	T	C	46	GENIC	homozygous	109501883
1	75705986	75705987	C	A	38	GENIC	homozygous	120867062
1	75704755	75704758	CAA		40	GENIC	homozygous	131575544
1	75698079	75698079		CA	45	GENIC	homozygous	131257301
1	75698215	75698215		T	40	GENIC	possibly homozygous	131257302
1	75704905	75704907	AC		35	GENIC	homozygous	131257303
1	75699110	75699111	A	C	20	GENIC	homozygous	131275716