chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109214740	109214741	C	T	15	GENIC	homozygous	51598776
10	109214754	109214755	G	GC	8	GENIC	homozygous	51598777
10	109215129	109215130	T	A	11	GENIC	homozygous	51598778
10	109215367	109215368	T	TG	7	GENIC	homozygous	51598779
10	109215664	109215665	T	-	10	GENIC	homozygous	51598782
10	109215676	109215677	T	C	11	GENIC	homozygous	51598783
10	109215937	109215938	G	A	20	GENIC	homozygous	51598786
10	109216311	109216312	A	G	17	GENIC	homozygous	51598788
10	109216367	109216368	A	G	13	GENIC	homozygous	51598789
10	109216569	109216570	G	A	15	GENIC	homozygous	51598790
10	109217006	109217007	C	CT	16	GENIC	homozygous	51598792
10	109218144	109218145	A	G	13	GENIC	homozygous	51598803
10	109218164	109218165	C	T	13	GENIC	homozygous	51598804
10	109218364	109218365	T	G	7	GENIC	homozygous	51598805
10	109218658	109218659	G	A	20	GENIC	homozygous	51598806
10	109218875	109218876	A	G	15	GENIC	homozygous	51598807
10	109218897	109218898	A	G	14	GENIC	homozygous	51598808
10	109218907	109218908	G	A	13	GENIC	homozygous	51598809
10	109219195	109219196	C	T	12	GENIC	homozygous	51598810
10	109219321	109219322	G	T	12	GENIC	homozygous	51598813
10	109219381	109219382	C	T	14	GENIC	homozygous	51598814
10	109219599	109219600	G	A	10	GENIC	homozygous	51598816
10	109219625	109219626	C	T	10	GENIC	homozygous	51598817