chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	92595659	92595660	T	TTG	15	GENIC	possibly homozygous	49962816
13	92596274	92596275	A	-	13	GENIC	heterozygous	50134633
13	92596881	92596882	A	AG	12	GENIC	homozygous	49859696
13	92596940	92596941	G	A	25	GENIC	homozygous	49859697
13	92597011	92597012	G	A	27	GENIC	homozygous	49859698
13	92597038	92597039	A	G	28	GENIC	homozygous	49859699
13	92597103	92597104	C	A	21	GENIC	homozygous	49962818
13	92597116	92597117	A	C	20	GENIC	homozygous	49859700
13	92598665	92598666	C	T	23	GENIC	heterozygous	50134635
13	92600350	92600351	G	GCACACA	10	GENIC	possibly homozygous	50134637
13	92600864	92600865	A	G	13	GENIC	heterozygous	49859702
13	92600901	92600904	GGT	---	6	GENIC	heterozygous	49859703
13	92601476	92601477	G	GGT	20	GENIC	possibly homozygous	49962830
13	92606836	92606838	TG	--	10	GENIC	heterozygous	49962844
13	92608263	92608264	C	CGT	3	GENIC	heterozygous	49962845
13	92608670	92608671	A	AGAG	15	GENIC	homozygous	49859704
13	92612569	92612570	G	GA	13	GENIC	homozygous	49859710
13	92615142	92615143	A	C	23	GENIC	heterozygous	50134639
13	92619844	92619845	G	GATT	5	GENIC	homozygous	49859711
13	92622720	92622721	T	C	11	GENIC	homozygous	49859712
13	92628084	92628085	C	A	22	GENIC	homozygous	49859713