chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	44039785	44039786	C	A	20	GENIC	homozygous	115850004
11	44040237	44040238	A	T	19	GENIC	homozygous	115850006
11	44040310	44040311	T	A	23	GENIC	homozygous	115850008
11	44040332	44040333	C	G	20	GENIC	homozygous	115850010
11	44040475	44040476	A	G	45	GENIC	homozygous	115850012
11	44041910	44041911	G	T	62	GENIC	homozygous	115850014
11	44042233	44042234	T	C	35	GENIC	homozygous	115850016
11	44043944	44043945	G	A	31	GENIC	homozygous	115850018
11	44044006	44044007	C	G	30	GENIC	homozygous	115850020
11	44044308	44044309	C	T	44	GENIC	homozygous	115850022
11	44044536	44044537	G	A	56	GENIC	homozygous	115850024
11	44044636	44044637	C	T	45	GENIC	homozygous	115850026
11	44045465	44045466	T	C	45	GENIC	homozygous	115850028
11	44045883	44045884	A	G	47	GENIC	homozygous	115850030
11	44045918	44045919	T	C	42	GENIC	homozygous	115850032
11	44048749	44048750	G	A	39	GENIC	homozygous	115850034
11	44048936	44048937	G	A	46	GENIC	homozygous	115850036
11	44049177	44049178	C	G	31	GENIC	homozygous	115850038
11	44049608	44049609	G	C	35	GENIC	homozygous	115850040