chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95770683	95770684	T	G	22	GENIC	possibly homozygous	116688144
10	95803078	95803078		G	8	GENIC	homozygous	128848817
10	95803082	95803082		G	8	GENIC	homozygous	128848818
10	95803097	95803097		G	11	GENIC	homozygous	128848819
10	95803102	95803102		G	10	GENIC	homozygous	128848820
10	95803107	95803107		G	11	GENIC	homozygous	128848821
10	95803155	95803156	T		17	GENIC	homozygous	128848823
10	95803159	95803159		T	17	GENIC	homozygous	128848824
10	95850924	95850924		C	47	GENIC	homozygous	128848836
10	95850944	95850944		A	39	GENIC	homozygous	128848837
10	95850991	95850991		T	29	GENIC	homozygous	128848838
10	95850995	95850995		C	28	GENIC	homozygous	128848839
10	95852082	95852083	T		49	GENIC	homozygous	128848841
10	95853002	95853003	A	G	11	GENIC	heterozygous	118009690
10	95865298	95865299	T	C	17	GENIC	heterozygous	118009693
10	95893814	95893814		G	48	GENIC	homozygous	128848853
10	95898290	95898290		AAATGTGTGCTTAGCAGGAAAGTGTAGGGAGCAAGGAATGACTCCAGCTCTCAGAGCCGGATGCTGCGGGGAGCACATATTTTTGGGAC	30	GENIC	homozygous	128848854
10	95830142	95830142		A	22	GENIC	homozygous	129970562
10	95830146	95830148	TG		19	GENIC	homozygous	129970563
10	95851074	95851075	T		13	GENIC	homozygous	129970564
10	95850976	95850977	C	T	34	GENIC	homozygous	117328786
10	95850978	95850979	T	A	34	GENIC	homozygous	117328788
10	95862178	95862179	G	A	47	GENIC	homozygous	134854830