chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90005127	90005129	GT	--	5	GENIC	homozygous	51537427
10	90005129	90005130	T	A	5	GENIC	homozygous	52508325
10	90005640	90005641	A	G	8	GENIC	homozygous	51537428
10	90005842	90005843	G	A	14	GENIC	possibly homozygous	51537429
10	90006332	90006333	T	-	1	GENIC	homozygous	51735635
10	90006357	90006358	G	-	2	GENIC	heterozygous	51537432
10	90006610	90006611	C	G	25	GENIC	homozygous	51537434
10	90007167	90007168	C	CT	1	GENIC	homozygous	51537439
10	90007279	90007280	A	G	12	GENIC	homozygous	51537440
10	90007480	90007481	C	-	9	GENIC	possibly homozygous	51537441
10	90008143	90008144	G	T	4	GENIC	homozygous	51537442
10	90008299	90008300	G	GGTCCGCCC	1	GENIC	homozygous	51537445
10	90009323	90009324	T	C	14	GENIC	possibly homozygous	51537446
10	90009360	90009361	A	AG	11	GENIC	heterozygous	52574864
10	90009721	90009722	G	A	24	GENIC	homozygous	51537447