chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	13866612	13866613	A	G	13	GENIC	homozygous	45435716
20	13867696	13867699	TCT	---	7	GENIC	heterozygous	45819804
20	13868771	13868774	CAG	---	13	GENIC	homozygous	45819805
20	13871502	13871503	T	TGGGGGCTACACTGGGGAGCTACACTG	3	GENIC	heterozygous	45819806
20	13871723	13871724	T	A	17	GENIC	homozygous	45819807
20	13871827	13871828	T	C	10	GENIC	heterozygous	45819808
20	13873650	13873651	G	T	11	GENIC	heterozygous	45819809
20	13873651	13873652	A	C	11	GENIC	heterozygous	45819810
20	13873934	13873935	C	T	15	GENIC	homozygous	45819811
20	13874554	13874555	A	-	3	GENIC	homozygous	45756863
20	13877356	13877357	G	A	19	GENIC	heterozygous	45819812
20	13878115	13878116	G	A	10	GENIC	heterozygous	45819813
20	13878770	13878771	A	G	33	GENIC	homozygous	45819814
20	13879017	13879018	C	T	25	GENIC	possibly homozygous	45819815
20	13879286	13879287	T	A	1	GENIC	homozygous	45435752
20	13879502	13879503	A	T	16	GENIC	possibly homozygous	45435754
20	13880509	13880510	T	-	4	GENIC	homozygous	45435760
20	13881421	13881422	C	T	21	GENIC	homozygous	45756868
20	13881893	13881900	GGCTCAG	-------	2	GENIC	homozygous	45819816
20	13882427	13882428	G	A	18	GENIC	homozygous	45819817
20	13882826	13882827	T	C	19	GENIC	homozygous	45819818
20	13885002	13885003	T	C	29	GENIC	possibly homozygous	45435776
20	13886096	13886097	T	C	3	GENIC	heterozygous	45435780
20	13886956	13886957	A	G	17	GENIC	possibly homozygous	45435786
20	13887435	13887436	C	A	16	GENIC	homozygous	45819819