chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95770682	95770682		TG	6	GENIC	heterozygous	133494052
10	95786173	95786173		T	19	GENIC	heterozygous	133232964
10	95803078	95803078		G	7	GENIC	homozygous	128848817
10	95803082	95803082		G	7	GENIC	homozygous	128848818
10	95803097	95803097		G	6	GENIC	homozygous	128848819
10	95803102	95803102		G	5	GENIC	homozygous	128848820
10	95803107	95803107		G	4	GENIC	homozygous	128848821
10	95803155	95803156	T		9	GENIC	homozygous	128848823
10	95803159	95803159		T	9	GENIC	homozygous	128848824
10	95830142	95830142		A	11	GENIC	homozygous	129970562
10	95830146	95830148	TG		11	GENIC	homozygous	129970563
10	95850924	95850924		C	18	GENIC	homozygous	128848836
10	95850944	95850944		A	18	GENIC	homozygous	128848837
10	95850991	95850991		T	14	GENIC	homozygous	128848838
10	95850995	95850995		C	13	GENIC	homozygous	128848839
10	95851074	95851075	T		9	GENIC	homozygous	129970564
10	95852082	95852083	T		19	GENIC	homozygous	128848841
10	95853002	95853003	A	G	6	GENIC	heterozygous	118009690
10	95865298	95865299	T	C	5	GENIC	homozygous	118009693
10	95879051	95879051		AGAT	11	GENIC	homozygous	128848850
10	95893814	95893814		G	17	GENIC	homozygous	128848853
10	95898290	95898290		AAATGTGTGCTTAGCAGGAAAGTGTAGGGAGCAAGGAATGACTCCAGCTCTCAGAGCCGGATGCTGCGGGGAGCACATATTTTTGGGAC	15	GENIC	homozygous	128848854
10	95850976	95850977	C	T	15	GENIC	homozygous	117328786
10	95850978	95850979	T	A	15	GENIC	homozygous	117328788