chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	2064739	2064740	T	C	22	GENIC	homozygous	51301000
10	2064838	2064840	TT	--	11	GENIC	homozygous	51301001
10	2065651	2065652	A	C	44	GENIC	homozygous	51301004
10	2065992	2065993	C	CTT	32	GENIC	homozygous	51301005
10	2066282	2066283	T	C	37	GENIC	homozygous	51301006
10	2068025	2068026	C	T	29	GENIC	homozygous	51301007
10	2068846	2068847	T	TA	28	GENIC	homozygous	51301008
10	2068912	2068913	G	A	29	GENIC	homozygous	51301009
10	2069085	2069086	C	T	33	GENIC	homozygous	51301010
10	2069141	2069142	C	CT	22	GENIC	possibly homozygous	51301011
10	2069434	2069435	G	A	24	GENIC	homozygous	51301012
10	2069891	2069892	G	-	35	GENIC	homozygous	51301013
10	2070749	2070750	A	G	35	GENIC	homozygous	51301014
10	2070831	2070832	C	T	29	GENIC	homozygous	51301015
10	2070852	2070855	AGG	---	32	GENIC	homozygous	51301016
10	2071329	2071330	A	G	40	GENIC	homozygous	51301017
10	2071589	2071590	G	A	23	GENIC	homozygous	51301018
10	2072603	2072605	CA	--	28	GENIC	homozygous	51301020
10	2072606	2072612	CCATCC	------	29	GENIC	homozygous	51301021
10	2072754	2072755	A	G	24	GENIC	homozygous	51301022
10	2072805	2072806	G	-	34	GENIC	homozygous	51301023
10	2072838	2072839	T	C	32	GENIC	homozygous	51301024
10	2072890	2072891	G	C	23	GENIC	homozygous	51301025
10	2073167	2073168	T	C	15	GENIC	homozygous	51301026
10	2080854	2080855	T	G	21	GENIC	homozygous	51301028
10	2082010	2082011	T	C	28	GENIC	homozygous	51301029
10	2082062	2082063	C	CGAGGCTGGGGGT	4	GENIC	homozygous	52760101
10	2082550	2082551	G	T	20	GENIC	homozygous	51301030
10	2084830	2084831	G	A	25	GENIC	homozygous	51301031
10	2084891	2084892	T	C	31	GENIC	homozygous	51301032
10	2086332	2086333	C	T	19	GENIC	homozygous	51301034
10	2086433	2086434	T	C	36	GENIC	homozygous	51301035
10	2086525	2086526	C	T	45	GENIC	homozygous	51301036
10	2086993	2086994	A	G	39	GENIC	homozygous	51301037
10	2088039	2088040	T	C	62	GENIC	homozygous	51301038