chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	37589844	37589844		T	26	GENIC	heterozygous	130149004
15	37609274	37609274		GCACACCTGTAATGTCAGCACTTG	27	GENIC	heterozygous	131739328
15	37609301	37609302	A		7	GENIC	homozygous	129246358
15	37609321	37609322	T	G	5	GENIC	homozygous	112807901
15	37636462	37636464	CG		20	GENIC	homozygous	129246361
15	37636475	37636475		G	16	GENIC	homozygous	129246362
15	37636480	37636480		GGGGA	14	GENIC	homozygous	129246363
15	37636486	37636487	A		14	GENIC	homozygous	129246364
15	37636498	37636499	A		15	GENIC	homozygous	129246365
15	37636500	37636501	G	A	15	GENIC	homozygous	124064695
15	37636517	37636518	A		16	GENIC	homozygous	129246366
15	37636521	37636521		G	16	GENIC	homozygous	129246367
15	37639578	37639578		TGGG	17	GENIC	homozygous	129246368
15	37639580	37639580		TTT	19	GENIC	homozygous	129246369
15	37639581	37639581		GCTCAGTGGT	21	GENIC	homozygous	129246370
15	37639584	37639585	A	C	24	GENIC	homozygous	124064702
15	37639584	37639584		GCG	23	GENIC	homozygous	129246371
15	37639589	37639589		CTAGCAAGCA	25	GENIC	homozygous	129246372
15	37644214	37644216	AG		23	GENIC	heterozygous	129246374
15	37661648	37661650	AC		44	GENIC	heterozygous	130149005