chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	78171816	78171817	C	CAG	8	GENIC	possibly homozygous	50834988
11	78172763	78172764	A	G	27	GENIC	homozygous	50834989
11	78172841	78172845	AAAC	----	19	GENIC	homozygous	50834990
11	78178748	78178749	C	G	27	GENIC	homozygous	51146945
11	78180078	78180079	A	ATGTGTG	3	GENIC	homozygous	51190306
11	78182435	78182436	C	-	5	GENIC	homozygous	50834992
11	78182521	78182522	G	GCAAGCGCTCTACCACTGAGCTAAATCCCCAA	3	GENIC	homozygous	51190307
11	78182727	78182729	AC	--	19	GENIC	homozygous	50834993
11	78183115	78183116	C	T	19	GENIC	homozygous	50834994
11	78183225	78183226	G	GC	24	GENIC	homozygous	50834995
11	78184494	78184495	C	CA	4	GENIC	heterozygous	51190308
11	78184495	78184496	A	-	4	GENIC	heterozygous	50834996
11	78187006	78187007	G	A	19	GENIC	homozygous	50895567
11	78187423	78187446	GGTGGTGCTACACCAAGAGGAGA	-----------------------	25	GENIC	homozygous	50834997
11	78187694	78187695	C	T	12	GENIC	homozygous	50834998
11	78187733	78187734	C	T	21	GENIC	homozygous	50834999
11	78188040	78188041	T	C	28	GENIC	homozygous	50835000
11	78188411	78188412	T	C	12	GENIC	homozygous	50835002
11	78188570	78188571	C	T	6	GENIC	homozygous	50835003
11	78188618	78188619	G	GC	15	GENIC	homozygous	50835004
11	78189060	78189061	G	A	22	GENIC	homozygous	50835005
11	78189100	78189101	A	AT	20	GENIC	homozygous	50835006
11	78189116	78189117	C	T	26	GENIC	homozygous	50835007
11	78189235	78189236	C	T	27	GENIC	homozygous	50835008
11	78189321	78189322	A	G	33	GENIC	homozygous	50835009