chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109726232	109726233	A	G	2	GENIC	homozygous	51957105
10	109726283	109726284	C	T	11	GENIC	possibly homozygous	51957108
10	109728194	109728195	G	T	13	GENIC	homozygous	51957111
10	109728309	109728310	G	C	17	GENIC	possibly homozygous	51957114
10	109729278	109729279	C	T	15	GENIC	homozygous	51957117
10	109729499	109729500	C	A	27	GENIC	homozygous	51957120
10	109729919	109729920	T	C	24	GENIC	possibly homozygous	51957123
10	109729953	109729954	C	CGAG	11	GENIC	possibly homozygous	51957126
10	109730203	109730204	T	C	7	GENIC	heterozygous	51957129
10	109730293	109730294	C	T	7	GENIC	homozygous	51957132
10	109730587	109730588	A	T	14	GENIC	homozygous	51957135
10	109731089	109731090	G	A	11	GENIC	possibly homozygous	51957138
10	109732945	109732946	A	AC	12	GENIC	homozygous	51957149
10	109733446	109733447	T	C	16	GENIC	possibly homozygous	51957152
10	109734004	109734005	G	A	26	GENIC	possibly homozygous	51599664
10	109734116	109734117	G	A	13	GENIC	possibly homozygous	51957155
10	109734440	109734441	T	C	13	GENIC	possibly homozygous	51957158