chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	7776093	7776094	A	G	20	GENIC	homozygous	45414571
20	7776805	7776806	C	G	19	GENIC	homozygous	45414572
20	7776832	7776833	C	A	18	GENIC	possibly homozygous	45677617
20	7776853	7776854	G	A	19	GENIC	homozygous	45677618
20	7777972	7777973	C	A	15	GENIC	homozygous	45414574
20	7780598	7780599	C	T	33	GENIC	homozygous	45789547
20	7780770	7780773	GGG	---	15	GENIC	heterozygous	45819035
20	7781102	7781103	G	A	21	GENIC	homozygous	45677622
20	7781457	7781459	AA	--	2	GENIC	homozygous	45855817
20	7781884	7781885	T	G	19	GENIC	homozygous	45414580
20	7782097	7782098	C	T	28	GENIC	homozygous	45677625
20	7783898	7783899	A	G	9	GENIC	homozygous	45677627
20	7784510	7784511	T	G	27	GENIC	homozygous	45414581
20	7784516	7784517	C	T	28	GENIC	homozygous	45789548
20	7785158	7785159	G	A	13	GENIC	possibly homozygous	45677630
20	7785974	7785975	T	C	21	GENIC	homozygous	45414582
20	7786307	7786311	CTAT	----	32	GENIC	homozygous	45677633
20	7786526	7786527	G	-	32	GENIC	homozygous	45414584
20	7787242	7787243	G	A	33	GENIC	homozygous	45677635
20	7787273	7787274	C	CAAGG	25	GENIC	homozygous	45677636