chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90813965	90813966	G	A	39	GENIC	homozygous	52165853
10	90814603	90814604	G	T	14	GENIC	homozygous	51737708
10	90815361	90815362	C	T	17	GENIC	homozygous	51737714
10	90816513	90816514	C	T	31	GENIC	homozygous	51737718
10	90817408	90817409	T	C	21	GENIC	homozygous	51737722
10	90817490	90817491	C	CA	20	GENIC	possibly homozygous	51737724
10	90817670	90817671	C	A	24	GENIC	homozygous	51737726
10	90818027	90818028	G	A	33	GENIC	homozygous	52165854
10	90818318	90818319	G	A	17	GENIC	homozygous	52165855
10	90818328	90818329	T	A	20	GENIC	homozygous	51737728
10	90818433	90818434	C	T	34	GENIC	homozygous	52165856
10	90818523	90818524	A	G	27	GENIC	homozygous	51737730
10	90818645	90818646	T	G	31	GENIC	homozygous	51737732
10	90819631	90819632	C	T	8	GENIC	homozygous	52165857