chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95955080	95955081	C	T	48	GENIC	homozygous	117022678
10	95955211	95955212	A	G	39	GENIC	homozygous	117413957
10	95955577	95955578	T	C	49	GENIC	homozygous	117022679
10	95955758	95955759	T	C	42	GENIC	homozygous	117022680
10	95956180	95956181	A	C	57	GENIC	homozygous	117022681
10	95956831	95956832	A	T	52	GENIC	homozygous	117022682
10	95956866	95956867	C	T	58	GENIC	homozygous	117022683
10	95957102	95957103	A	G	60	GENIC	homozygous	117022684
10	95957193	95957194	A	G	60	GENIC	homozygous	117022685
10	95957603	95957604	C	T	42	GENIC	homozygous	117022686
10	95955892	95955939	GAGTGCTCTCCAACACCAGGAAGCACTTTCCTGGTGTTGGAGAGCAC		31	GENIC	homozygous	133233013
10	95965482	95965484	TG		18	GENIC	heterozygous	130682383
10	95967110	95967110		AG	26	GENIC	heterozygous	130682384
10	95968002	95968003	G		19	GENIC	homozygous	128848904
10	95968014	95968015	T		16	GENIC	homozygous	128848905
10	96003413	96003414	G	C	19	GENIC	homozygous	116688784
10	96003605	96003606	A	T	12	GENIC	heterozygous	132333968
10	96003609	96003610	T	A	10	GENIC	heterozygous	132333969
10	96003532	96003536	CCAC		17	GENIC	heterozygous	130394482