chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	82023378	82023379	G	A	30	GENIC	homozygous	51716979
10	82023415	82023416	C	CAG	30	GENIC	heterozygous	51516433
10	82023508	82023512	ACAC	----	4	GENIC	heterozygous	51516436
10	82023531	82023532	C	G	14	GENIC	heterozygous	51516437
10	82023642	82023644	AC	--	8	GENIC	homozygous	51516439
10	82023708	82023709	T	C	9	GENIC	heterozygous	51516440
10	82023752	82023753	A	AC	5	GENIC	heterozygous	51516441
10	82023794	82023795	G	GAC	10	GENIC	heterozygous	51716981
10	82024001	82024002	C	T	30	GENIC	homozygous	51516442
10	82024078	82024082	GTGT	----	9	GENIC	heterozygous	51516443
10	82024080	82024082	GT	--	9	GENIC	heterozygous	51516444
10	82024319	82024320	C	A	26	GENIC	homozygous	51516445
10	82024326	82024327	C	T	27	GENIC	homozygous	51516446
10	82024454	82024455	T	C	36	GENIC	homozygous	51516447
10	82025015	82025016	G	GTACCTC	15	GENIC	homozygous	52068386
10	82025334	82025335	C	T	36	GENIC	homozygous	51516448
10	82026000	82026001	G	A	29	GENIC	possibly homozygous	51516449
10	82028014	82028015	G	GA	14	GENIC	possibly homozygous	51516451
10	82028360	82028361	T	TG	8	GENIC	homozygous	52068388
10	82028891	82028892	T	G	21	GENIC	homozygous	51516454
10	82029768	82029770	AC	--	10	GENIC	heterozygous	51716983
10	82029813	82029814	C	CAG	12	GENIC	homozygous	51516456
10	82023525	82023526	G	C	11	GENIC	heterozygous	51991911
10	82023527	82023528	T	C	12	GENIC	heterozygous	51991914