chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46728770	46728771	G	T	30	GENIC	possibly homozygous	51637116
10	46732917	46732918	C	T	38	GENIC	homozygous	51637117
10	46733775	46733776	A	-	12	GENIC	possibly homozygous	51637118
10	46736956	46736957	T	A	45	GENIC	possibly homozygous	51445172
10	46737006	46737007	T	C	34	GENIC	homozygous	51445173
10	46737575	46737582	CACTGCC	-------	16	GENIC	homozygous	51445175
10	46737773	46737774	C	T	29	GENIC	homozygous	51445177
10	46738393	46738394	T	C	25	GENIC	homozygous	51445178
10	46739054	46739055	A	G	43	GENIC	possibly homozygous	51445179
10	46739194	46739195	G	T	26	GENIC	homozygous	51445180
10	46739629	46739630	A	G	13	GENIC	homozygous	51445181
10	46739632	46739672	CTGATTTTCAGGCCACCTCCCCGGCCCAGTCACATAGCTA	----------------------------------------	24	GENIC	possibly homozygous	51445182
10	46739706	46739707	G	A	18	GENIC	possibly homozygous	51445183
10	46740138	46740139	A	G	34	GENIC	homozygous	51445184
10	46740291	46740292	A	G	17	GENIC	homozygous	51445185
10	46741220	46741221	T	C	35	GENIC	homozygous	51445188
10	46741606	46741607	T	C	18	GENIC	homozygous	51445189
10	46741700	46741701	C	CT	21	GENIC	homozygous	51637119
10	46741885	46741886	T	G	19	GENIC	homozygous	51445190
10	46742110	46742111	T	TGG	12	GENIC	homozygous	51445191
10	46742360	46742361	G	A	27	GENIC	homozygous	51637120