chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	70622843	70622844	A	C	22	GENIC	homozygous	53392560
8	70623003	70623004	T	G	25	GENIC	homozygous	53392561
8	70623792	70623793	G	A	21	GENIC	homozygous	53392562
8	70624061	70624062	T	G	18	GENIC	homozygous	53392563
8	70624321	70624322	C	T	20	GENIC	homozygous	53392564
8	70625668	70625669	C	CATGT	17	GENIC	possibly homozygous	53392565
8	70625798	70625799	A	ATGTG	12	GENIC	homozygous	53392566
8	70625821	70625822	C	T	18	GENIC	homozygous	53392567
8	70626164	70626165	T	G	21	GENIC	homozygous	53392568
8	70626238	70626239	C	T	24	GENIC	homozygous	53392569
8	70627877	70627878	G	A	18	GENIC	homozygous	53392570
8	70629521	70629522	G	-	24	GENIC	homozygous	53392571
8	70625817	70625818	C	T	20	GENIC	homozygous	52673389