chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	44039785	44039786	C	A	53	GENIC	homozygous	115850004
11	44040237	44040238	A	T	45	GENIC	homozygous	115850006
11	44040332	44040333	C	G	59	GENIC	homozygous	115850010
11	44040554	44040555	G	A	52	GENIC	homozygous	116132500
11	44040711	44040712	T	C	67	GENIC	possibly homozygous	116132502
11	44042233	44042234	T	C	48	GENIC	homozygous	115850016
11	44043600	44043601	C	T	66	GENIC	possibly homozygous	116132504
11	44043620	44043621	C	A	63	GENIC	possibly homozygous	116132506
11	44044006	44044007	C	G	67	GENIC	homozygous	115850020
11	44044488	44044489	C	T	35	GENIC	homozygous	116132508
11	44045465	44045466	T	C	45	GENIC	homozygous	115850028
11	44045918	44045919	T	C	38	GENIC	homozygous	115850032
11	44045972	44045973	A	G	32	GENIC	homozygous	116132510
11	44047926	44047927	A	G	47	GENIC	possibly homozygous	116132512
11	44046936	44046936		T	34	GENIC	possibly homozygous	131478820
11	44048416	44048416		G	25	GENIC	homozygous	131478822
11	44042385	44042385		TT	32	GENIC	homozygous	131478818
11	44045688	44045688		T	39	GENIC	homozygous	131478819
11	44048102	44048104	TG		32	GENIC	possibly homozygous	131478821
11	44042388	44042389	A	G	37	GENIC	homozygous	116353976
11	44044821	44044822	G	A	18	GENIC	homozygous	116353977
11	44044626	44044626		T	39	GENIC	homozygous	128905957
11	44048459	44048460	G	T	30	GENIC	homozygous	116132514
11	44048488	44048489	C	A	30	GENIC	possibly homozygous	116353978
11	44048726	44048727	G	T	41	GENIC	possibly homozygous	116132516
11	44049177	44049178	C	G	51	GENIC	homozygous	115850038
11	44049608	44049609	G	C	65	GENIC	homozygous	115850040