chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	2650133	2650134	T		40	GENIC	homozygous	128878924
11	2650160	2650160		A	42	GENIC	homozygous	128878925
11	2650192	2650192		G	39	GENIC	homozygous	128878926
11	2650198	2650198		G	38	GENIC	homozygous	128878927
11	2650207	2650207		G	40	GENIC	homozygous	128878928
11	2650250	2650250		T	34	GENIC	homozygous	128878929
11	2650460	2650460		G	16	GENIC	homozygous	128878930
11	2650462	2650462		C	17	GENIC	homozygous	128878931
11	2650466	2650466		CC	17	GENIC	homozygous	128878932
11	2650470	2650470		C	17	GENIC	homozygous	128878933
11	2657818	2657819	C		7	GENIC	homozygous	128878934
11	2657827	2657828	C		12	GENIC	homozygous	128878935
11	2657836	2657836		T	15	GENIC	homozygous	128878936
11	2657843	2657844	G		16	GENIC	homozygous	128878937
11	2657851	2657852	A		19	GENIC	homozygous	128878938
11	2657859	2657860	G		26	GENIC	homozygous	128878939
11	2657871	2657872	C		27	GENIC	homozygous	128878940
11	2657908	2657908		C	32	GENIC	homozygous	128878941
11	2657915	2657916	T	A	34	GENIC	homozygous	116013755
11	2657910	2657911	C	A	34	GENIC	homozygous	115945577
11	2657833	2657834	T	G	15	GENIC	homozygous	115945572
11	2657903	2657904	G	T	32	GENIC	homozygous	115945574