chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	92595660	92595662	TG	--	6	GENIC	heterozygous	50530599
13	92596220	92596221	C	CGGAAA	9	GENIC	homozygous	50530601
13	92596449	92596450	G	GA	17	GENIC	heterozygous	50658677
13	92596881	92596882	A	AG	20	GENIC	homozygous	49859696
13	92596940	92596941	G	A	17	GENIC	homozygous	49859697
13	92597011	92597012	G	A	30	GENIC	homozygous	49859698
13	92597038	92597039	A	G	32	GENIC	homozygous	49859699
13	92597103	92597104	C	A	31	GENIC	homozygous	49962818
13	92597104	92597105	A	G	31	GENIC	homozygous	50497370
13	92597116	92597117	A	C	28	GENIC	homozygous	49859700
13	92600864	92600865	A	AGGAGAAGGAGGAGAAGGAGGAGGGAGAGGAGGAGGAGAAGGAGGAGGG	4	GENIC	heterozygous	50530603
13	92600903	92600904	T	G	4	GENIC	homozygous	50530605
13	92601476	92601477	G	GGT	23	GENIC	possibly homozygous	49962830
13	92608693	92608694	A	AGCACAAAAAATGGCAGTTGTT	28	GENIC	homozygous	50530607
13	92611773	92611775	TG	--	1	GENIC	homozygous	50530609
13	92619844	92619845	G	GATTATT	2	GENIC	homozygous	50530613
13	92621906	92621908	TG	--	22	GENIC	heterozygous	50584911
13	92622720	92622721	T	C	13	GENIC	homozygous	49859712
13	92600870	92600871	A	-	6	GENIC	heterozygous	50566404
13	92600873	92600877	AGAA	----	6	GENIC	heterozygous	50566405
13	92601477	92601479	GT	--	23	GENIC	heterozygous	50566406
13	92608264	92608268	GTGT	----	6	GENIC	heterozygous	50566407
13	92608263	92608264	C	CGTGT	6	GENIC	heterozygous	50603196
13	92609274	92609276	GT	--	4	GENIC	heterozygous	50812506
13	92627614	92627616	CA	--	16	GENIC	heterozygous	50530614
13	92628084	92628085	C	A	19	GENIC	homozygous	49859713
13	92629614	92629615	C	T	28	GENIC	homozygous	49962906
13	92629615	92629616	T	A	28	GENIC	homozygous	50497376