chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95362652	95362653	C	T	16	GENIC	possibly homozygous	68932558
10	95363392	95363393	A	G	26	GENIC	homozygous	68186761
10	95364837	95364838	T	C	18	GENIC	homozygous	68186781
10	95365430	95365431	T	C	13	GENIC	homozygous	68932560
10	95366431	95366432	T	G	30	GENIC	homozygous	68186794
10	95366525	95366526	G	A	22	GENIC	homozygous	68186798
10	95369383	95369384	T	C	25	GENIC	homozygous	68471358
10	95371004	95371005	A	G	17	GENIC	homozygous	68471361
10	95371916	95371917	G	A	30	GENIC	possibly homozygous	68186810
10	95371922	95371923	T	A	29	GENIC	possibly homozygous	68186815
10	95372837	95372838	C	T	22	GENIC	possibly homozygous	68471364
10	95373457	95373458	T	C	19	GENIC	homozygous	68186823
10	95374120	95374121	A	G	24	GENIC	homozygous	68186827
10	95374494	95374495	T	C	35	GENIC	homozygous	68186831
10	95375569	95375570	G	A	29	GENIC	possibly homozygous	68471367
10	95376018	95376019	G	A	22	GENIC	homozygous	68186834
10	95377062	95377063	G	A	20	GENIC	homozygous	68471373
10	95377294	95377295	T	C	20	GENIC	homozygous	68471376
10	95377307	95377308	T	C	22	GENIC	possibly homozygous	68471379
10	95377361	95377362	G	A	23	GENIC	homozygous	68471382
10	95378459	95378460	C	A	21	GENIC	homozygous	68186838
10	95378520	95378521	C	T	24	GENIC	homozygous	68186842
10	95378570	95378571	T	C	17	GENIC	homozygous	68186846
10	95378701	95378702	C	T	22	GENIC	homozygous	68186850
10	95378830	95378831	T	C	22	GENIC	homozygous	68186854
10	95378958	95378959	C	T	30	GENIC	possibly homozygous	68186857
10	95379887	95379888	G	A	24	GENIC	homozygous	68186861
10	95379937	95379938	C	T	22	GENIC	homozygous	68471387
10	95380155	95380156	C	T	25	GENIC	homozygous	68186865
10	95381019	95381020	G	A	20	GENIC	possibly homozygous	68186873