chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109214712	109214713	T	A	28	GENIC	possibly homozygous	51955818
10	109214754	109214755	G	GC	11	GENIC	homozygous	51598777
10	109214803	109214804	G	T	14	GENIC	homozygous	51955821
10	109215129	109215130	T	A	25	GENIC	homozygous	51598778
10	109215752	109215753	G	A	19	GENIC	possibly homozygous	51955824
10	109216311	109216312	A	G	25	GENIC	homozygous	51598788
10	109216367	109216368	A	G	23	GENIC	possibly homozygous	51598789
10	109216462	109216463	C	T	26	GENIC	possibly homozygous	51955827
10	109216569	109216570	G	A	26	GENIC	homozygous	51598790
10	109217685	109217686	G	A	24	GENIC	homozygous	51955833
10	109217909	109217910	C	T	12	GENIC	heterozygous	51955836
10	109218144	109218145	A	G	36	GENIC	possibly homozygous	51598803
10	109218549	109218550	C	T	34	GENIC	possibly homozygous	51955842
10	109218897	109218898	A	G	27	GENIC	possibly homozygous	51598808
10	109219247	109219248	G	A	14	GENIC	possibly homozygous	51955845