chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	92595659	92595660	T	TTG	10	GENIC	possibly homozygous	49962816
13	92596274	92596275	A	-	7	GENIC	homozygous	50134633
13	92596881	92596882	A	AG	22	GENIC	homozygous	49859696
13	92596940	92596941	G	A	40	GENIC	homozygous	49859697
13	92597011	92597012	G	A	24	GENIC	homozygous	49859698
13	92597038	92597039	A	G	24	GENIC	homozygous	49859699
13	92597116	92597117	A	C	23	GENIC	homozygous	49859700
13	92600350	92600351	G	GCACACA	19	GENIC	heterozygous	50134637
13	92600864	92600865	A	G	21	GENIC	heterozygous	49859702
13	92600880	92600881	G	-	19	GENIC	heterozygous	49962827
13	92600901	92600904	GGT	---	12	GENIC	heterozygous	49859703
13	92601476	92601477	G	GGT	19	GENIC	heterozygous	49962830
13	92608263	92608264	C	CGT	7	GENIC	possibly homozygous	49962845
13	92608670	92608671	A	AGAG	19	GENIC	homozygous	49859704
13	92609320	92609321	G	-	24	GENIC	heterozygous	49962847
13	92609320	92609321	G	GT	25	GENIC	heterozygous	49962848
13	92612569	92612570	G	GA	11	GENIC	homozygous	49859710
13	92622720	92622721	T	C	13	GENIC	possibly homozygous	49859712
13	92628084	92628085	C	A	20	GENIC	homozygous	49859713