chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4181703	4181704	A	G	17	GENIC	homozygous	50002658
12	4182013	4182014	T	G	21	GENIC	homozygous	50002659
12	4183748	4183749	T	C	13	GENIC	homozygous	50002668
12	4183780	4183781	C	T	15	GENIC	homozygous	50002669
12	4184020	4184021	T	TG	11	GENIC	homozygous	50002670
12	4185057	4185058	T	-	10	GENIC	homozygous	50002673
12	4185366	4185367	C	T	17	GENIC	homozygous	50002674
12	4186643	4186644	T	TA	19	GENIC	homozygous	50002677
12	4186819	4186820	A	T	16	GENIC	homozygous	50002678
12	4186893	4186894	G	A	18	GENIC	homozygous	50002679
12	4187448	4187449	G	T	22	GENIC	homozygous	50002680
12	4187763	4187764	A	G	15	GENIC	homozygous	50002681
12	4188564	4188565	T	C	12	GENIC	homozygous	50002682
12	4188573	4188575	AA	--	8	GENIC	homozygous	50357777
12	4189290	4189291	C	T	9	GENIC	homozygous	50002684
12	4189737	4189738	C	-	8	GENIC	homozygous	50002685
12	4190041	4190042	C	T	12	GENIC	homozygous	50002686
12	4193044	4193045	A	G	21	GENIC	homozygous	50394240
12	4195372	4195373	A	AT	13	GENIC	homozygous	50002696