chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105568153	105568154	A	G	17	GENIC	homozygous	116837132
10	105568214	105568215	A	T	7	GENIC	homozygous	116837134
10	105568539	105568540	A	G	12	GENIC	homozygous	116837136
10	105568777	105568778	T	C	17	GENIC	homozygous	116837138
10	105569232	105569233	T	C	10	GENIC	homozygous	116837142
10	105569499	105569500	C	T	15	GENIC	homozygous	116837144
10	105569518	105569519	A	G	10	GENIC	homozygous	116837146
10	105569583	105569584	C	T	24	GENIC	homozygous	116837148
10	105569639	105569640	G	A	8	GENIC	homozygous	116837150
10	105569650	105569651	C	T	9	GENIC	homozygous	116837152
10	105569707	105569708	T	C	19	GENIC	homozygous	116837154
10	105570223	105570224	T	G	31	GENIC	possibly homozygous	126489858
10	105570269	105570270	G	C	6	GENIC	homozygous	126489859
10	105570381	105570382	T	G	7	GENIC	heterozygous	126489860
10	105570431	105570432	T	C	4	GENIC	homozygous	126489861
10	105570489	105570490	A	G	16	GENIC	heterozygous	126489862
10	105570520	105570521	T	C	8	GENIC	heterozygous	126489863
10	105570678	105570679	G	A	9	GENIC	homozygous	126489864
10	105570721	105570722	G	A	20	GENIC	homozygous	117279828
10	105570831	105570832	T	C	19	GENIC	homozygous	116837156
10	105571011	105571012	G	A	15	GENIC	homozygous	116837158
10	105571015	105571016	G	A	17	GENIC	homozygous	116837160
10	105572049	105572050	G	T	8	GENIC	homozygous	116837162
10	105572123	105572124	C	G	13	GENIC	homozygous	116837164
10	105572362	105572363	T	C	8	GENIC	homozygous	116837166