chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	68860183	68860184	A	G	51	GENIC	homozygous	111853744
16	68860976	68860977	A	G	18	GENIC	homozygous	111853745
16	68861421	68861430	CACAGGCAG		13	GENIC	homozygous	129377021
16	68863271	68863272	G	T	53	GENIC	homozygous	111853746
16	68863612	68863613	T	A	47	GENIC	homozygous	111853747
16	68863875	68863876	A	G	41	GENIC	homozygous	111853748
16	68864093	68864094	C	A	38	GENIC	homozygous	112023524
16	68864096	68864097	C	A	39	GENIC	homozygous	111853749
16	68864335	68864336	A	G	42	GENIC	homozygous	111853750
16	68865021	68865022	G	A	32	GENIC	homozygous	111853751
16	68865189	68865190	G	A	44	GENIC	homozygous	111853752
16	68865334	68865335	A	G	42	GENIC	homozygous	111853753
16	68865392	68865393	C	A	27	GENIC	homozygous	112023526
16	68865512	68865513	C	T	28	GENIC	homozygous	111853754
16	68865651	68865652	A	G	26	GENIC	homozygous	111853755
16	68865707	68865708	A		15	GENIC	homozygous	129377022
16	68866024	68866025	C	T	37	GENIC	homozygous	112023528
16	68866224	68866225	G	A	32	GENIC	homozygous	112023530
16	68866310	68866311	T	C	39	GENIC	homozygous	112023532
16	68866434	68866435	C	A	47	GENIC	possibly homozygous	112023534
16	68866581	68866582	G	A	44	GENIC	homozygous	112023537
16	68866637	68866638	T	C	53	GENIC	homozygous	112023539
16	68866659	68866659		TGTTG	51	GENIC	homozygous	129377024
16	68866373	68866373		T	43	GENIC	possibly homozygous	131180522
16	68866307	68866307		T	40	GENIC	homozygous	131180521