chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	150852482	150852483	T	C	33	GENIC	homozygous	55794700
5	150853766	150853767	A	AC	17	GENIC	homozygous	55794701
5	150854917	150854918	T	TC	32	GENIC	homozygous	55794702
5	150856488	150856489	T	C	19	GENIC	homozygous	55794703
5	150856822	150856823	T	C	17	GENIC	homozygous	55794704
5	150861254	150861255	T	C	36	GENIC	homozygous	55794705
5	150861395	150861397	GG	--	2	GENIC	homozygous	55924151
5	150861551	150861552	G	A	25	GENIC	homozygous	55794706
5	150862573	150862574	T	G	35	GENIC	homozygous	55794707
5	150862814	150862815	A	G	35	GENIC	homozygous	55794708
5	150863651	150863652	T	C	28	GENIC	homozygous	55794709
5	150864055	150864056	T	C	47	GENIC	homozygous	55794710
5	150868793	150868794	T	C	21	GENIC	homozygous	55794711
5	150869360	150869361	G	GTCT	36	GENIC	homozygous	55794713
5	150869741	150869742	G	A	31	GENIC	homozygous	55794714
5	150869835	150869836	T	-	12	GENIC	heterozygous	55794715
5	150869836	150869837	G	-	2	GENIC	homozygous	55794716
5	150870837	150870847	ACACACACAC	----------	15	GENIC	homozygous	55794717
5	150871332	150871333	A	-	30	GENIC	homozygous	55794718
5	150872333	150872351	TCTCTCTCTCTCTCTCTC	------------------	4	GENIC	homozygous	55794719
5	150872488	150872489	G	A	33	GENIC	homozygous	55794720
5	150872861	150872862	A	T	39	GENIC	homozygous	55794721
5	150873017	150873018	C	G	14	GENIC	homozygous	55794722
5	150873233	150873234	G	-	15	GENIC	heterozygous	55794723
5	150873238	150873239	A	G	15	GENIC	heterozygous	56128883
5	150873491	150873492	G	A	12	GENIC	homozygous	55794724
5	150873867	150873868	C	CA	13	GENIC	homozygous	55794725
5	150874179	150874180	G	A	26	GENIC	homozygous	55794726
5	150875288	150875289	T	C	16	GENIC	homozygous	55794727
5	150875739	150875740	T	-	11	GENIC	homozygous	55794728
5	150876339	150876340	A	ACCCAGG	23	GENIC	homozygous	55794729
5	150876584	150876587	CCC	---	8	GENIC	homozygous	55794730
5	150876830	150876831	A	G	28	GENIC	homozygous	55794732
5	150876941	150876942	C	CCTTT	21	GENIC	homozygous	55794733
5	150878000	150878001	C	T	42	GENIC	homozygous	55794734