chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	51986190	51986191	A	T	31	GENIC	homozygous	114763826
13	51986237	51986238	T	C	26	GENIC	homozygous	114763828
13	51986522	51986523	T	C	10	GENIC	homozygous	114763830
13	51986806	51986807	C	T	20	GENIC	homozygous	114763832
13	51988597	51988598	G	C	21	GENIC	homozygous	114763834
13	51988797	51988798	C	T	23	GENIC	homozygous	114763836
13	51988816	51988817	C	G	24	GENIC	homozygous	114763838
13	51989893	51989894	T	A	28	GENIC	homozygous	114763840
13	51990048	51990049	C	A	37	GENIC	homozygous	114763842
13	51990250	51990251	A	T	27	GENIC	homozygous	114763844
13	51990255	51990256	G	A	27	GENIC	homozygous	114763846
13	51992355	51992356	G	A	26	GENIC	homozygous	114763848