chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	162676333	162676334	A	T	19	GENIC	homozygous	108345577
1	162677227	162677228	A	G	18	GENIC	possibly homozygous	108345579
1	162677828	162677829	G	C	19	GENIC	possibly homozygous	108345583
1	162679968	162679969	C	G	34	GENIC	possibly homozygous	108345585
1	162680699	162680700	G	A	38	GENIC	possibly homozygous	108345587
1	162680958	162680959	G	A	30	GENIC	possibly homozygous	108345589
1	162682035	162682036	C	T	32	GENIC	possibly homozygous	108345591
1	162683276	162683277	C	T	20	GENIC	possibly homozygous	108345597
1	162683381	162683382	C	T	36	GENIC	homozygous	108345599
1	162683510	162683511	G	A	29	GENIC	homozygous	108345601
1	162683694	162683695	C	T	22	GENIC	possibly homozygous	108345603
1	162684997	162684998	C	G	28	GENIC	homozygous	108345605
1	162686223	162686224	A	T	36	GENIC	possibly homozygous	108345609
1	162686427	162686428	A	C	30	GENIC	possibly homozygous	108345611
1	162686528	162686529	G	T	22	GENIC	possibly homozygous	108345613
1	162686741	162686742	G	A	35	GENIC	possibly homozygous	108345615
1	162687262	162687263	C	T	22	GENIC	possibly homozygous	108345617
1	162687420	162687421	C	T	21	GENIC	possibly homozygous	108345619
1	162688058	162688059	A	C	33	GENIC	homozygous	120474377
1	162688357	162688358	T	G	19	GENIC	homozygous	108345621
1	162689859	162689860	T	G	36	GENIC	homozygous	108751148
1	162690141	162690142	G	A	31	GENIC	possibly homozygous	108345623
1	162693183	162693184	A	G	31	GENIC	possibly homozygous	108345625
1	162693931	162693932	C	T	24	GENIC	homozygous	108345627
1	162696407	162696408	G	T	26	GENIC	possibly homozygous	108345629