chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109396476	109396477	A	G	44	GENIC	homozygous	51599162
10	109398388	109398389	T	C	51	GENIC	homozygous	51599163
10	109399173	109399175	TT	--	17	GENIC	heterozygous	52085287
10	109399174	109399175	T	-	17	GENIC	heterozygous	51599164
10	109399760	109399761	T	C	50	GENIC	homozygous	51599165
10	109399877	109399878	G	A	53	GENIC	homozygous	51599166
10	109401070	109401071	A	G	53	GENIC	possibly homozygous	51599167
10	109401200	109401201	A	T	39	GENIC	homozygous	51599168
10	109401421	109401422	T	C	31	GENIC	homozygous	51599169
10	109402180	109402181	C	T	48	GENIC	homozygous	51599170
10	109402201	109402202	T	C	47	GENIC	homozygous	51599171
10	109402277	109402278	A	AT	46	GENIC	homozygous	51599172
10	109402611	109402612	C	A	47	GENIC	homozygous	51599173
10	109403437	109403438	A	G	30	GENIC	homozygous	51599174
10	109403734	109403735	T	C	26	GENIC	homozygous	51599175