chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97652185	97652186	C	T	14	GENIC	homozygous	51557724
10	97652300	97652301	C	T	6	GENIC	homozygous	51557725
10	97652450	97652451	A	G	6	GENIC	homozygous	51557726
10	97652541	97652544	GTG	---	4	GENIC	homozygous	51557727
10	97652590	97652602	AAACAAACAAAC	------------	8	GENIC	homozygous	53171143
10	97652614	97652615	A	T	5	GENIC	homozygous	52767315
10	97652625	97652626	T	C	7	GENIC	homozygous	51557729
10	97652697	97652698	A	AT	8	GENIC	homozygous	51557730
10	97652721	97652722	A	G	6	GENIC	homozygous	51557731
10	97652839	97652840	G	A	8	GENIC	homozygous	51557732
10	97652845	97652846	A	G	7	GENIC	homozygous	51557733
10	97652848	97652849	T	C	7	GENIC	homozygous	51557734
10	97652982	97652983	T	C	7	GENIC	homozygous	51557735
10	97653509	97653510	T	C	8	GENIC	homozygous	51557736
10	97653554	97653555	G	A	11	GENIC	homozygous	51557737
10	97653657	97653658	A	ATG	5	GENIC	heterozygous	51751463
10	97653657	97653658	A	ATGTG	5	GENIC	heterozygous	51751466
10	97653765	97653766	C	CTCTG	7	GENIC	homozygous	53171145
10	97653976	97653977	T	C	7	GENIC	homozygous	51557739
10	97654117	97654118	G	GTTTTT	2	GENIC	homozygous	52812043
10	97654128	97654129	C	T	4	GENIC	homozygous	52767318
10	97654169	97654170	A	G	2	GENIC	homozygous	52876550
10	97654173	97654174	G	T	2	GENIC	homozygous	52876552
10	97654267	97654268	T	C	5	GENIC	homozygous	53171147
10	97654268	97654269	T	C	5	GENIC	homozygous	53171149
10	97654292	97654293	A	-	4	GENIC	heterozygous	51751469
10	97654323	97654324	A	G	9	GENIC	homozygous	53171151
10	97654347	97654348	T	C	10	GENIC	homozygous	53171153
10	97654449	97654450	A	T	6	GENIC	homozygous	53171155
10	97654579	97654580	A	G	12	GENIC	homozygous	53171156
10	97654732	97654733	T	C	5	GENIC	homozygous	53171158