chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105123791	105123792	G	A	44	GENIC	homozygous	117031637
10	105123810	105123811	T	C	43	GENIC	homozygous	116836409
10	105125075	105125076	T	C	26	GENIC	homozygous	116836411
10	105125538	105125539	T	C	54	GENIC	homozygous	117031639
10	105126519	105126520	G	A	12	GENIC	homozygous	116836417
10	105126809	105126810	C	A	62	GENIC	homozygous	117031641
10	105127784	105127785	A	G	34	GENIC	homozygous	116836421
10	105128186	105128187	G	A	47	GENIC	homozygous	117031643
10	105128829	105128830	A	C	40	GENIC	homozygous	117031645
10	105128915	105128916	A	C	39	GENIC	homozygous	116836423
10	105129137	105129138	G	A	39	GENIC	homozygous	116836425
10	105131165	105131166	C	T	43	GENIC	homozygous	117031647
10	105131808	105131809	G	C	25	GENIC	homozygous	117031649
10	105132870	105132871	T	C	35	GENIC	homozygous	117031651
10	105133298	105133299	A	C	88	GENIC	homozygous	116836435
10	105134506	105134507	G	A	48	GENIC	homozygous	117031655
10	105134890	105134891	C	T	60	GENIC	homozygous	117031657
10	105135787	105135788	C	T	10	GENIC	homozygous	117031659
10	105135808	105135809	T	A	3	GENIC	homozygous	117031661
10	105136137	105136138	G	A	24	GENIC	homozygous	117031663
10	105136355	105136356	T	C	59	GENIC	homozygous	117031665
10	105136798	105136799	T	C	30	GENIC	homozygous	116836441
10	105135066	105135067	G	T	39	GENIC	homozygous	117260855