chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4181703	4181704	A	G	23	GENIC	homozygous	50002658
12	4182013	4182014	T	G	19	GENIC	homozygous	50002659
12	4182245	4182246	G	A	3	GENIC	homozygous	50002661
12	4182246	4182247	T	A	4	GENIC	homozygous	50002662
12	4182874	4182875	T	A	23	GENIC	possibly homozygous	50002664
12	4183053	4183054	C	T	5	GENIC	homozygous	50002665
12	4183678	4183687	TTCTTTTTT	---------	2	GENIC	heterozygous	50526376
12	4183780	4183781	C	T	12	GENIC	possibly homozygous	50002669
12	4184020	4184021	T	TG	9	GENIC	possibly homozygous	50002670
12	4185057	4185058	T	-	4	GENIC	homozygous	50002673
12	4185366	4185367	C	T	18	GENIC	homozygous	50002674
12	4186643	4186644	T	TA	12	GENIC	heterozygous	50002677
12	4186819	4186820	A	T	13	GENIC	possibly homozygous	50002678
12	4186893	4186894	G	A	9	GENIC	homozygous	50002679
12	4187448	4187449	G	T	16	GENIC	possibly homozygous	50002680
12	4187763	4187764	A	G	13	GENIC	homozygous	50002681
12	4189290	4189291	C	T	7	GENIC	homozygous	50002684
12	4189737	4189738	C	-	5	GENIC	heterozygous	50002685
12	4190041	4190042	C	T	11	GENIC	possibly homozygous	50002686
12	4191789	4191790	C	CTCTCTCTCTG	1	GENIC	homozygous	50526394
12	4194041	4194042	A	T	1	GENIC	homozygous	50002693
12	4194145	4194146	A	AC	1	GENIC	homozygous	50002694
12	4194510	4194511	C	CAG	10	GENIC	possibly homozygous	50002695
12	4195372	4195373	A	AT	1	GENIC	homozygous	50002696