chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	37589844	37589844		T	18	GENIC	heterozygous	130149004
15	37609275	37609276	G	C	5	GENIC	homozygous	112807899
15	37609301	37609302	A		5	GENIC	homozygous	129246358
15	37636462	37636464	CG		6	GENIC	homozygous	129246361
15	37636475	37636475		G	6	GENIC	homozygous	129246362
15	37636480	37636480		GGGGA	6	GENIC	homozygous	129246363
15	37636486	37636487	A		4	GENIC	homozygous	129246364
15	37636498	37636499	A		5	GENIC	homozygous	129246365
15	37636500	37636501	G	A	6	GENIC	homozygous	124064695
15	37636517	37636518	A		8	GENIC	homozygous	129246366
15	37636521	37636521		G	8	GENIC	homozygous	129246367
15	37639578	37639578		TGGG	3	GENIC	homozygous	129246368
15	37639580	37639580		TTT	5	GENIC	homozygous	129246369
15	37639581	37639581		GCTCAGTGGT	7	GENIC	homozygous	129246370
15	37639584	37639585	A	C	11	GENIC	homozygous	124064702
15	37639584	37639584		GCG	10	GENIC	homozygous	129246371
15	37639589	37639589		CTAGCAAGCA	11	GENIC	homozygous	129246372
15	37661648	37661650	AC		8	GENIC	heterozygous	130149005
15	37609320	37609321	T	G	3	GENIC	homozygous	112988048
15	37631130	37631130		G	4	GENIC	heterozygous	131159480