chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109214712	109214713	T	A	21	GENIC	homozygous	51955818
10	109214754	109214755	G	GC	21	GENIC	homozygous	51598777
10	109214803	109214804	G	T	23	GENIC	homozygous	51955821
10	109215129	109215130	T	A	32	GENIC	homozygous	51598778
10	109215752	109215753	G	A	12	GENIC	homozygous	51955824
10	109216311	109216312	A	G	34	GENIC	homozygous	51598788
10	109216367	109216368	A	G	23	GENIC	homozygous	51598789
10	109216462	109216463	C	T	31	GENIC	homozygous	51955827
10	109216569	109216570	G	A	29	GENIC	homozygous	51598790
10	109216985	109216986	C	CTATCTATCTATCTATCT	6	GENIC	homozygous	52734622
10	109217234	109217246	TCTGTCTATCTA	------------	5	GENIC	homozygous	52409941
10	109217685	109217686	G	A	22	GENIC	homozygous	51955833
10	109217909	109217910	C	T	15	GENIC	homozygous	51955836
10	109217932	109217933	C	CTT	9	GENIC	possibly homozygous	52409943
10	109218144	109218145	A	G	20	GENIC	homozygous	51598803
10	109218549	109218550	C	T	24	GENIC	homozygous	51955842
10	109218897	109218898	A	G	37	GENIC	homozygous	51598808
10	109219247	109219248	G	A	22	GENIC	homozygous	51955845
10	109219316	109219317	G	GTTT	9	GENIC	homozygous	51598811
10	109219321	109219322	G	T	10	GENIC	homozygous	51598813