chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95362153	95362154	A	C	53	GENIC	homozygous	68186757
10	95363392	95363393	A	G	45	GENIC	homozygous	68186761
10	95363937	95363938	G	A	42	GENIC	homozygous	68186764
10	95364054	95364055	G	A	43	GENIC	homozygous	68186768
10	95364308	95364309	G	A	49	GENIC	homozygous	68186773
10	95364357	95364358	A	G	47	GENIC	homozygous	68186777
10	95364837	95364838	T	C	31	GENIC	homozygous	68186781
10	95365164	95365165	C	T	41	GENIC	homozygous	68186785
10	95365201	95365202	C	T	40	GENIC	homozygous	68186789
10	95366431	95366432	T	G	53	GENIC	homozygous	68186794
10	95366525	95366526	G	A	36	GENIC	homozygous	68186798
10	95368374	95368375	G	A	31	GENIC	homozygous	68186803
10	95371916	95371917	G	A	46	GENIC	homozygous	68186810
10	95371922	95371923	T	A	46	GENIC	homozygous	68186815
10	95373259	95373260	G	A	61	GENIC	homozygous	68186819
10	95373457	95373458	T	C	40	GENIC	homozygous	68186823
10	95374120	95374121	A	G	42	GENIC	homozygous	68186827
10	95374494	95374495	T	C	38	GENIC	homozygous	68186831
10	95376018	95376019	G	A	52	GENIC	homozygous	68186834
10	95378459	95378460	C	A	49	GENIC	homozygous	68186838
10	95378520	95378521	C	T	46	GENIC	homozygous	68186842
10	95378570	95378571	T	C	43	GENIC	homozygous	68186846
10	95378701	95378702	C	T	42	GENIC	homozygous	68186850
10	95378830	95378831	T	C	38	GENIC	possibly homozygous	68186854
10	95378958	95378959	C	T	52	GENIC	homozygous	68186857
10	95379887	95379888	G	A	31	GENIC	homozygous	68186861
10	95380155	95380156	C	T	39	GENIC	homozygous	68186865
10	95380878	95380879	G	A	46	GENIC	homozygous	68186869
10	95381019	95381020	G	A	44	GENIC	homozygous	68186873