chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	16729136	16729137	T	-	11	GENIC	heterozygous	62224775
1	16729448	16729450	CA	--	15	GENIC	heterozygous	62120498
1	16731056	16731057	C	-	29	GENIC	homozygous	60635411
1	16731436	16731437	A	AT	23	GENIC	heterozygous	62252594
1	16731437	16731438	T	-	23	GENIC	heterozygous	62252595
1	16733231	16733233	GT	--	19	GENIC	heterozygous	62224776
1	16737559	16737562	TAA	---	42	GENIC	homozygous	60635413
1	16743681	16743682	T	TG	21	GENIC	homozygous	60635414
1	16745078	16745079	C	CGTGT	6	GENIC	homozygous	62120500
1	16748955	16748956	G	-	43	GENIC	homozygous	60635415
1	16752097	16752098	C	CTT	8	GENIC	heterozygous	62120501
1	16763004	16763005	G	-	4	GENIC	homozygous	60635416
1	16768757	16768758	A	G	9	GENIC	homozygous	60635417
1	16768783	16768784	C	A	8	GENIC	homozygous	62120504
1	16768785	16768786	T	A	10	GENIC	homozygous	62120505
1	16768786	16768787	G	A	10	GENIC	homozygous	62120506
1	16768789	16768790	T	A	10	GENIC	homozygous	62120507
1	16768797	16768798	T	A	15	GENIC	homozygous	62120508
1	16768799	16768800	C	A	16	GENIC	homozygous	60635420
1	16768804	16768805	C	A	18	GENIC	homozygous	62120509
1	16768806	16768807	T	A	18	GENIC	homozygous	62120510
1	16768808	16768809	C	A	20	GENIC	homozygous	62120511
1	16768809	16768810	C	A	20	GENIC	homozygous	62120512
1	16768825	16768826	C	-	23	GENIC	homozygous	60635421
1	16769036	16769037	G	GC	20	GENIC	homozygous	60635422