chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	162676333	162676334	A	T	20	GENIC	homozygous	108345577
1	162677227	162677228	A	G	30	GENIC	homozygous	108345579
1	162679968	162679969	C	G	41	GENIC	homozygous	108345585
1	162680699	162680700	G	A	41	GENIC	homozygous	108345587
1	162682035	162682036	C	T	32	GENIC	homozygous	108345591
1	162682547	162682548	T	G	30	GENIC	homozygous	108345595
1	162683276	162683277	C	T	42	GENIC	homozygous	108345597
1	162683381	162683382	C	T	45	GENIC	homozygous	108345599
1	162683510	162683511	G	A	39	GENIC	homozygous	108345601
1	162683694	162683695	C	T	37	GENIC	homozygous	108345603
1	162684997	162684998	C	G	37	GENIC	homozygous	108345605
1	162685742	162685743	G	T	21	GENIC	homozygous	108345607
1	162686223	162686224	A	T	45	GENIC	homozygous	108345609
1	162686427	162686428	A	C	24	GENIC	homozygous	108345611
1	162686528	162686529	G	T	25	GENIC	homozygous	108345613
1	162686741	162686742	G	A	44	GENIC	homozygous	108345615
1	162687262	162687263	C	T	28	GENIC	homozygous	108345617
1	162688058	162688059	A	C	40	GENIC	homozygous	120474377
1	162688357	162688358	T	G	38	GENIC	homozygous	108345621
1	162689859	162689860	T	G	32	GENIC	homozygous	108751148
1	162690141	162690142	G	A	41	GENIC	homozygous	108345623
1	162693183	162693184	A	G	32	GENIC	homozygous	108345625
1	162693931	162693932	C	T	18	GENIC	homozygous	108345627
1	162696407	162696408	G	T	39	GENIC	homozygous	108345629