chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	51509489	51509490	A		42	GENIC	heterozygous	130392590
10	51548782	51548783	A	C	59	GENIC	homozygous	116594416
10	51554657	51554657		G	26	GENIC	homozygous	128817098
10	51561007	51561008	T	C	20	GENIC	homozygous	123358740
10	51561007	51561007		C	20	GENIC	homozygous	128817103
10	51561010	51561015	TGTTA		20	GENIC	homozygous	128817104
10	51561017	51561017		TAGG	19	GENIC	homozygous	128817105
10	51561020	51561022	AA		19	GENIC	homozygous	128817106
10	51561026	51561027	G	C	18	GENIC	homozygous	123358745
10	51561028	51561029	T	C	18	GENIC	homozygous	123358746
10	51565326	51565327	G		15	GENIC	heterozygous	130392591
10	51561070	51561071	G	A	19	GENIC	homozygous	117078291
10	51586004	51586005	C	A	34	GENIC	possibly homozygous	117994137
10	51594207	51594207		C	16	GENIC	homozygous	128817118
10	51594212	51594213	G		16	GENIC	homozygous	128817119
10	51594260	51594262	GC		28	GENIC	homozygous	128817120
10	51594295	51594295		A	31	GENIC	homozygous	128817121
10	51594299	51594299		G	32	GENIC	homozygous	128817122
10	51594372	51594372		T	40	GENIC	homozygous	128817123
10	51594379	51594379		T	39	GENIC	homozygous	128817124
10	51594468	51594469	G	A	31	GENIC	homozygous	116594522
10	51656353	51656353		C	51	GENIC	homozygous	128817148
10	51594446	51594446		T	35	GENIC	homozygous	128817125
10	51594480	51594480		A	32	GENIC	homozygous	128817126
10	51594507	51594507		T	27	GENIC	homozygous	128817127
10	51594517	51594517		C	27	GENIC	homozygous	128817128
10	51657396	51657396		C	43	GENIC	homozygous	128817149
10	51657400	51657400		AC	43	GENIC	homozygous	128817150
10	51657408	51657409	C		39	GENIC	homozygous	128817151
10	51657530	51657530		TGT	38	GENIC	homozygous	128817152
10	51657527	51657528	C	G	39	GENIC	homozygous	116884939
10	51657684	51657684		C	6	GENIC	homozygous	129969015