chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	95969698	95969699	C	T	26	GENIC	homozygous	117119718
8	95971452	95971453	C	T	38	GENIC	homozygous	117119720
8	95972100	95972101	A	C	29	GENIC	homozygous	117119722
8	95972301	95972302	A	G	26	GENIC	homozygous	117119724
8	95972461	95972462	G	A	33	GENIC	homozygous	117119726
8	95972523	95972524	C	T	27	GENIC	homozygous	116588541
8	95973389	95973390	C	T	27	GENIC	homozygous	117119728
8	95973905	95973906	G	A	25	GENIC	homozygous	117119730
8	95974270	95974271	G	A	36	GENIC	homozygous	117119732
8	95975109	95975110	T	C	21	GENIC	homozygous	117119734
8	95975172	95975173	C	G	26	GENIC	homozygous	116588547
8	95976798	95976799	C	T	31	GENIC	homozygous	117119736
8	95982752	95982753	T	G	28	GENIC	possibly homozygous	116588623
8	95984330	95984331	T	A	27	GENIC	homozygous	117119738
8	95992542	95992543	G	T	30	GENIC	homozygous	117119740
8	95994097	95994098	C	T	22	GENIC	homozygous	117119742
8	95995191	95995192	C	T	28	GENIC	heterozygous	117119744
8	95999373	95999374	A	T	36	GENIC	homozygous	116588639
8	96001732	96001733	T	C	35	GENIC	possibly homozygous	116588643
8	96004703	96004704	C	T	34	GENIC	homozygous	117119746
8	96004808	96004809	A	G	26	GENIC	homozygous	116853830
8	96004964	96004965	A	G	25	GENIC	homozygous	116588649
8	96007003	96007004	G	C	44	GENIC	homozygous	116588653
8	96007140	96007141	A	G	35	GENIC	homozygous	116588655
8	96008127	96008128	G	A	27	GENIC	possibly homozygous	116588657
8	96009827	96009828	G	A	33	GENIC	homozygous	116588659
8	96012571	96012572	G	A	24	GENIC	possibly homozygous	116588661