chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109396476	109396477	A	G	32	GENIC	homozygous	51599162
10	109398234	109398235	G	A	22	GENIC	heterozygous	51956481
10	109398388	109398389	T	C	5	GENIC	homozygous	51599163
10	109399760	109399761	T	C	14	GENIC	homozygous	51599165
10	109399877	109399878	G	A	29	GENIC	possibly homozygous	51599166
10	109400303	109400304	C	G	14	GENIC	possibly homozygous	51956484
10	109401070	109401071	A	G	23	GENIC	homozygous	51599167
10	109401200	109401201	A	T	15	GENIC	homozygous	51599168
10	109401421	109401422	T	C	28	GENIC	homozygous	51599169
10	109402180	109402181	C	T	25	GENIC	possibly homozygous	51599170
10	109402201	109402202	T	C	19	GENIC	homozygous	51599171
10	109402277	109402278	A	AT	13	GENIC	homozygous	51599172
10	109402340	109402341	G	GTGTGTGCA	3	GENIC	heterozygous	51956487
10	109402611	109402612	C	A	19	GENIC	homozygous	51599173
10	109403437	109403438	A	G	22	GENIC	homozygous	51599174
10	109403734	109403735	T	C	12	GENIC	homozygous	51599175