chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	76088896	76088897	C	A	34	GENIC	possibly homozygous	53336187
10	76089855	76089856	A	G	21	GENIC	homozygous	51499986
10	76090236	76090237	T	A	17	GENIC	homozygous	53336188
10	76092465	76092467	TT	--	17	GENIC	homozygous	51499989
10	76093045	76093046	G	A	24	GENIC	homozygous	53336189
10	76093423	76093424	T	C	24	GENIC	homozygous	53336190
10	76094262	76094263	G	GGTGTAT	26	GENIC	homozygous	53336191
10	76094512	76094513	C	T	34	GENIC	homozygous	53336192
10	76094577	76094578	A	G	27	GENIC	homozygous	51499991
10	76095957	76095958	A	-	16	GENIC	homozygous	52568034
10	76096330	76096351	CCACTGAGCTAAATCCCCAAC	---------------------	13	GENIC	homozygous	53336193
10	76096610	76096611	T	C	21	GENIC	possibly homozygous	53336194
10	76096629	76096630	G	GAAAC	12	GENIC	homozygous	53336195
10	76096748	76096749	A	G	32	GENIC	homozygous	51499997
10	76096985	76096986	T	A	22	GENIC	possibly homozygous	51499998
10	76097296	76097297	G	A	32	GENIC	homozygous	52568039
10	76097394	76097395	A	G	33	GENIC	possibly homozygous	51499999
10	76097934	76097935	T	C	22	GENIC	possibly homozygous	53336196
10	76098236	76098237	T	A	15	GENIC	homozygous	53336197