chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	150852482	150852483	T	C	14	GENIC	possibly homozygous	55794700
5	150853766	150853767	A	AC	2	GENIC	heterozygous	55794701
5	150854917	150854918	T	TC	18	GENIC	homozygous	55794702
5	150856488	150856489	T	C	14	GENIC	homozygous	55794703
5	150856822	150856823	T	C	17	GENIC	homozygous	55794704
5	150861254	150861255	T	C	7	GENIC	heterozygous	55794705
5	150861395	150861398	GGG	---	2	GENIC	heterozygous	56460656
5	150861396	150861398	GG	--	2	GENIC	heterozygous	56356402
5	150861551	150861552	G	A	13	GENIC	homozygous	55794706
5	150862573	150862574	T	G	20	GENIC	homozygous	55794707
5	150862814	150862815	A	G	16	GENIC	homozygous	55794708
5	150863651	150863652	T	C	14	GENIC	homozygous	55794709
5	150864055	150864056	T	C	16	GENIC	possibly homozygous	55794710
5	150868793	150868794	T	C	15	GENIC	homozygous	55794711
5	150868874	150868875	T	-	2	GENIC	homozygous	55794712
5	150869360	150869361	G	GTCT	6	GENIC	homozygous	55794713
5	150869741	150869742	G	A	7	GENIC	possibly homozygous	55794714
5	150869836	150869837	G	-	5	GENIC	homozygous	55794716
5	150870837	150870849	ACACACACACAC	------------	2	GENIC	heterozygous	56554469
5	150871332	150871333	A	-	6	GENIC	homozygous	55794718
5	150872488	150872489	G	A	19	GENIC	homozygous	55794720
5	150872861	150872862	A	T	32	GENIC	homozygous	55794721
5	150873017	150873018	C	G	1	GENIC	homozygous	55794722
5	150873491	150873492	G	A	27	GENIC	homozygous	55794724
5	150874179	150874180	G	A	22	GENIC	homozygous	55794726
5	150875288	150875289	T	C	9	GENIC	heterozygous	55794727
5	150876339	150876340	A	ACCCAGG	6	GENIC	homozygous	55794729
5	150876830	150876831	A	G	14	GENIC	possibly homozygous	55794732
5	150876941	150876942	C	CCTTT	2	GENIC	homozygous	55794733
5	150878000	150878001	C	T	20	GENIC	possibly homozygous	55794734