chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95362153	95362154	A	C	23	GENIC	homozygous	68186757
10	95363392	95363393	A	G	32	GENIC	homozygous	68186761
10	95363937	95363938	G	A	26	GENIC	homozygous	68186764
10	95364054	95364055	G	A	34	GENIC	homozygous	68186768
10	95364308	95364309	G	A	47	GENIC	homozygous	68186773
10	95364357	95364358	A	G	37	GENIC	homozygous	68186777
10	95364837	95364838	T	C	20	GENIC	homozygous	68186781
10	95366431	95366432	T	G	31	GENIC	homozygous	68186794
10	95368447	95368448	G	A	20	GENIC	homozygous	82721455
10	95364927	95364928	A	G	20	GENIC	homozygous	69813434
10	95366606	95366607	G	A	18	GENIC	homozygous	69813435
10	95367746	95367747	G	A	9	GENIC	homozygous	82721453
10	95367914	95367915	T	A	26	GENIC	homozygous	82721454
10	95371759	95371760	A	C	34	GENIC	homozygous	69813437
10	95371922	95371923	T	A	31	GENIC	homozygous	68186815
10	95373457	95373458	T	C	33	GENIC	homozygous	68186823
10	95373923	95373924	G	A	33	GENIC	homozygous	69813438
10	95374228	95374229	C	T	31	GENIC	homozygous	69813439
10	95374494	95374495	T	C	20	GENIC	homozygous	68186831
10	95376018	95376019	G	A	30	GENIC	homozygous	68186834
10	95376075	95376076	C	T	20	GENIC	homozygous	69813440
10	95376310	95376311	T	C	32	GENIC	homozygous	69813441
10	95378459	95378460	C	A	28	GENIC	homozygous	68186838
10	95378520	95378521	C	T	22	GENIC	homozygous	68186842
10	95378570	95378571	T	C	32	GENIC	homozygous	68186846
10	95378830	95378831	T	C	24	GENIC	homozygous	68186854
10	95378958	95378959	C	T	32	GENIC	homozygous	68186857
10	95379300	95379301	C	A	32	GENIC	homozygous	82721456
10	95379466	95379467	T	C	30	GENIC	homozygous	69813443
10	95379887	95379888	G	A	38	GENIC	homozygous	68186861
10	95380155	95380156	C	T	30	GENIC	homozygous	68186865