chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	171656101	171656102	T	C	41	GENIC	homozygous	55839859
5	171656314	171656319	GGTTC	-----	9	GENIC	heterozygous	55839860
5	171656327	171656328	C	-	7	GENIC	homozygous	55839861
5	171656398	171656399	A	G	34	GENIC	homozygous	55839862
5	171656403	171656404	T	G	39	GENIC	homozygous	55839863
5	171656444	171656446	CG	--	41	GENIC	homozygous	55839864
5	171656447	171656452	CCGAC	-----	49	GENIC	homozygous	55839865
5	171656467	171656468	C	T	50	GENIC	homozygous	55839866
5	171656596	171656597	T	C	29	GENIC	homozygous	55839867
5	171656645	171656646	C	T	19	GENIC	homozygous	55839868
5	171656872	171656873	T	C	36	GENIC	homozygous	55839869
5	171657737	171657738	C	G	70	GENIC	homozygous	55839873
5	171657995	171657996	C	T	32	GENIC	homozygous	55839874
5	171658091	171658092	T	G	32	GENIC	homozygous	55839875
5	171658539	171658540	G	C	34	GENIC	homozygous	55839876
5	171658736	171658737	T	G	49	GENIC	homozygous	55839877
5	171659005	171659006	C	CT	37	GENIC	homozygous	55839878
5	171659820	171659821	T	C	50	GENIC	homozygous	55839879
5	171659879	171659880	G	T	74	GENIC	homozygous	55839880
5	171659883	171659884	T	G	70	GENIC	homozygous	55839881
5	171660011	171660012	T	C	56	GENIC	homozygous	55839882
5	171660423	171660424	T	C	40	GENIC	homozygous	55839883