chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	36021978	36021979	G	C	39	GENIC	homozygous	46106554
19	36022658	36022659	T	C	40	GENIC	homozygous	46106556
19	36023133	36023136	GGG	---	28	GENIC	heterozygous	46106558
19	36023134	36023136	GG	--	28	GENIC	possibly homozygous	46106560
19	36024224	36024225	C	CTG	40	GENIC	homozygous	46106562
19	36024507	36024508	G	A	53	GENIC	homozygous	46106564
19	36027625	36027626	A	G	70	GENIC	possibly homozygous	46106566
19	36027800	36027801	T	G	39	GENIC	homozygous	46106568
19	36031333	36031334	T	C	54	GENIC	homozygous	46106570
19	36031892	36031893	A	-	7	GENIC	homozygous	46106572
19	36032484	36032485	C	T	46	GENIC	homozygous	46106574
19	36034917	36034918	A	AGG	12	GENIC	homozygous	46106576
19	36034921	36034922	T	-	12	GENIC	homozygous	46106578
19	36034925	36034926	C	-	12	GENIC	homozygous	46106580
19	36039451	36039452	T	TA	54	GENIC	homozygous	46106582
19	36040181	36040182	A	G	64	GENIC	homozygous	46106584
19	36040534	36040541	TTAAAAA	-------	13	GENIC	homozygous	46106586
19	36042361	36042362	C	T	52	GENIC	homozygous	46106588
19	36043278	36043279	T	C	45	GENIC	homozygous	46106590
19	36043531	36043532	G	A	54	GENIC	homozygous	46106592
19	36043608	36043609	T	C	47	GENIC	homozygous	46106594
19	36043751	36043752	T	C	51	GENIC	possibly homozygous	46106596
19	36043966	36043967	C	T	68	GENIC	homozygous	46106598
19	36044593	36044594	G	-	47	GENIC	homozygous	46106600
19	36046467	36046468	T	G	30	GENIC	heterozygous	46106602