chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4054804	4054805	T	TTTTTG	12	GENIC	heterozygous	45374702
20	4055152	4055153	C	CAA	15	GENIC	homozygous	45374705
20	4056308	4056309	T	C	17	GENIC	homozygous	45374707
20	4056804	4056805	C	-	26	GENIC	homozygous	45772981
20	4056881	4056882	A	G	28	GENIC	homozygous	45374708
20	4058346	4058347	G	A	22	GENIC	homozygous	45374710
20	4058585	4058586	C	T	13	GENIC	homozygous	45374711
20	4059105	4059106	C	T	24	GENIC	homozygous	45374712
20	4059249	4059250	G	A	20	GENIC	homozygous	45374713
20	4059351	4059352	A	ATGTGTGTGTGTGTGTGTGTGTG	8	GENIC	homozygous	45861852
20	4059429	4059430	A	G	18	GENIC	homozygous	45374715
20	4060055	4060056	C	T	25	GENIC	homozygous	45374717
20	4060099	4060100	A	-	16	GENIC	homozygous	45374718
20	4060140	4060141	G	C	22	GENIC	homozygous	45374719
20	4060177	4060178	C	T	27	GENIC	homozygous	45374720
20	4060227	4060228	T	A	28	GENIC	homozygous	45374721
20	4060353	4060354	C	T	11	GENIC	homozygous	45374722
20	4060853	4060854	C	T	11	GENIC	homozygous	45374723