chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4054805	4054806	T	TTTTG	3	GENIC	homozygous	45374703
20	4055152	4055153	C	CAA	17	GENIC	possibly homozygous	45374705
20	4055723	4055724	C	T	11	GENIC	possibly homozygous	45374706
20	4056308	4056309	T	C	11	GENIC	homozygous	45374707
20	4056881	4056882	A	G	21	GENIC	possibly homozygous	45374708
20	4058346	4058347	G	A	24	GENIC	possibly homozygous	45374710
20	4058585	4058586	C	T	14	GENIC	homozygous	45374711
20	4059105	4059106	C	T	16	GENIC	possibly homozygous	45374712
20	4059249	4059250	G	A	17	GENIC	possibly homozygous	45374713
20	4059429	4059430	A	G	13	GENIC	homozygous	45374715
20	4059816	4059817	C	T	18	GENIC	possibly homozygous	45374716
20	4060055	4060056	C	T	15	GENIC	homozygous	45374717
20	4060099	4060100	A	-	12	GENIC	homozygous	45374718
20	4060140	4060141	G	C	11	GENIC	possibly homozygous	45374719
20	4060177	4060178	C	T	14	GENIC	possibly homozygous	45374720
20	4060227	4060228	T	A	20	GENIC	homozygous	45374721
20	4060353	4060354	C	T	11	GENIC	possibly homozygous	45374722
20	4060853	4060854	C	T	7	GENIC	homozygous	45374723