chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13448752	13448753	C	T	43	GENIC	homozygous	117249101
10	13451500	13451501	T	C	60	GENIC	homozygous	116496072
10	13453425	13453426	A	G	47	GENIC	homozygous	116496076
10	13455975	13455976	A	G	44	GENIC	homozygous	116496080
10	13462591	13462592	T	C	34	GENIC	homozygous	117982325
10	13463146	13463147	C	T	40	GENIC	homozygous	116496096
10	13470115	13470116	T	C	46	GENIC	homozygous	116496106
10	13471369	13471370	C	T	40	GENIC	homozygous	117249103
10	13474318	13474319	T	C	47	GENIC	homozygous	116496112
10	13494442	13494443	C	T	34	GENIC	homozygous	116496138
10	13453119	13453119		AA	43	GENIC	homozygous	131463454
10	13464148	13464148		T	37	GENIC	possibly homozygous	131463455
10	13480453	13480460	GTCACTT		46	GENIC	homozygous	131463456
10	13453542	13453542		ACCACCAGC	36	GENIC	homozygous	131087690
10	13458981	13458983	AC		37	GENIC	heterozygous	130681384
10	13464157	13464158	A	T	37	GENIC	homozygous	117277118
10	13494630	13494631	C	T	43	GENIC	homozygous	117277120
10	13497044	13497045	T	A	51	GENIC	homozygous	117277122
10	13497713	13497714	C	A	45	GENIC	possibly homozygous	116915322
10	13500208	13500209	A	T	32	GENIC	possibly homozygous	117277124
10	13506880	13506881	A	G	37	GENIC	homozygous	116496158
10	13508933	13508934	C	T	35	GENIC	homozygous	116496162
10	13516311	13516311		TT	27	GENIC	homozygous	131463457
10	13518188	13518189	A		37	GENIC	homozygous	128790616
10	13518487	13518488	T	C	41	GENIC	homozygous	116496176
10	13519885	13519885		TA	33	GENIC	homozygous	131463458
10	13520883	13520884	C	T	52	GENIC	possibly homozygous	117249105
10	13522926	13522927	A	T	27	GENIC	homozygous	117277126
10	13523159	13523160	C	A	42	GENIC	homozygous	116496180
10	13523232	13523232		G	44	GENIC	homozygous	131463459
10	13523574	13523575	A	C	51	GENIC	homozygous	116496182
10	13524307	13524308	A	G	38	GENIC	homozygous	116496184
10	13524493	13524494	T	A	56	GENIC	homozygous	116496186