chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	10047052	10047053	G	A	25	GENIC	homozygous	50041191
12	10047068	10047069	A	ATATGTATG	14	GENIC	homozygous	50529647
12	10047493	10047494	A	T	29	GENIC	homozygous	50041193
12	10048169	10048170	T	A	24	GENIC	homozygous	50041197
12	10048178	10048179	C	T	25	GENIC	homozygous	50041199
12	10048261	10048262	T	C	25	GENIC	homozygous	50041201
12	10048631	10048632	A	AAAT	4	GENIC	homozygous	50041204
12	10059441	10059443	TG	--	4	GENIC	heterozygous	50567952
12	10059997	10059998	G	C	18	GENIC	homozygous	50041206
12	10059999	10060000	G	C	20	GENIC	homozygous	50041208
12	10061272	10061273	C	-	14	GENIC	homozygous	50041210
12	10061308	10061309	T	G	20	GENIC	homozygous	50041212
12	10061758	10061759	T	G	24	GENIC	possibly homozygous	50041214
12	10061880	10061881	A	G	11	GENIC	homozygous	50041216
12	10062285	10062286	A	C	18	GENIC	homozygous	50041218
12	10062361	10062362	C	T	15	GENIC	homozygous	50041220
12	10062521	10062522	C	CGTGTGT	12	GENIC	heterozygous	50041222
12	10062521	10062522	C	CGTGT	12	GENIC	heterozygous	50529657
12	10062806	10062807	C	T	14	GENIC	homozygous	50041224
12	10063050	10063051	A	G	18	GENIC	homozygous	50041226