chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90005127	90005129	GT	--	29	GENIC	homozygous	51537427
10	90005640	90005641	A	G	29	GENIC	possibly homozygous	51537428
10	90005842	90005843	G	A	31	GENIC	homozygous	51537429
10	90006227	90006228	A	G	19	GENIC	homozygous	51537430
10	90006239	90006240	A	AAAAAG	16	GENIC	heterozygous	51537431
10	90006357	90006358	G	-	22	GENIC	homozygous	51537432
10	90006486	90006487	C	T	26	GENIC	possibly homozygous	51537433
10	90006610	90006611	C	G	37	GENIC	homozygous	51537434
10	90006908	90006911	TTT	---	18	GENIC	heterozygous	51537435
10	90006909	90006911	TT	--	18	GENIC	possibly homozygous	51537436
10	90007098	90007099	T	TTC	20	GENIC	heterozygous	51537438
10	90007167	90007168	C	CT	17	GENIC	possibly homozygous	51537439
10	90007279	90007280	A	G	31	GENIC	homozygous	51537440
10	90007480	90007481	C	-	25	GENIC	homozygous	51537441
10	90008143	90008144	G	T	18	GENIC	possibly homozygous	51537442
10	90008179	90008180	G	-	19	GENIC	heterozygous	51537443
10	90008179	90008180	G	GT	19	GENIC	heterozygous	51537444
10	90008299	90008300	G	GGTCCGCCC	13	GENIC	homozygous	51537445
10	90009323	90009324	T	C	27	GENIC	homozygous	51537446
10	90009721	90009722	G	A	38	GENIC	homozygous	51537447