chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	61460385	61460386	T	-	3	GENIC	heterozygous	51670503
10	61463698	61463699	C	T	8	GENIC	possibly homozygous	51670511
10	61464726	61464727	A	T	15	GENIC	homozygous	51899796
10	61468452	61468453	G	GGAT	1	GENIC	homozygous	51899798
10	61471244	61471245	A	G	12	GENIC	homozygous	51899800
10	61471920	61471921	C	A	10	GENIC	homozygous	51899802
10	61474450	61474451	T	G	2	GENIC	heterozygous	51670529
10	61474881	61474882	C	T	7	GENIC	homozygous	51899804
10	61477979	61477980	C	T	9	GENIC	heterozygous	51470881
10	61535184	61535185	A	G	9	GENIC	homozygous	51670558
10	61535916	61535917	T	A	4	GENIC	heterozygous	51899810
10	61537976	61537982	GGGAGT	------	3	GENIC	heterozygous	51470900
10	61541468	61541469	G	GATT	7	GENIC	heterozygous	51899814
10	61545370	61545371	A	C	11	GENIC	possibly homozygous	51899816
10	61546108	61546109	C	CA	9	GENIC	homozygous	51470903
10	61549765	61549766	G	A	9	GENIC	possibly homozygous	51899820
10	61549896	61549897	T	TG	7	GENIC	homozygous	51670574
10	61549945	61549946	C	T	3	GENIC	homozygous	51899822
10	61551119	61551120	A	G	7	GENIC	homozygous	51470904
10	61552224	61552225	A	G	10	GENIC	homozygous	51470905
10	61554254	61554255	G	T	11	GENIC	homozygous	51470908
10	61557440	61557441	G	A	9	GENIC	homozygous	51899826
10	61558496	61558497	G	A	4	GENIC	homozygous	51899828
10	61560746	61560747	G	A	9	GENIC	homozygous	51899830
10	61565333	61565334	G	GA	2	GENIC	homozygous	51470911
10	61566303	61566304	G	A	15	GENIC	possibly homozygous	51899834
10	61567916	61567917	G	T	2	GENIC	homozygous	51470913
10	61568700	61568701	T	C	10	GENIC	homozygous	51470914
10	61570797	61570798	A	G	14	GENIC	homozygous	51670612
10	61533510	61533512	GC	--	2	GENIC	homozygous	52319782
10	61533514	61533516	GC	--	1	GENIC	homozygous	52319784
10	61553062	61553063	C	CTT	5	GENIC	heterozygous	52319786