chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	82962993	82962993		C	16	GENIC	homozygous	128929052
11	82966419	82966420	G		24	GENIC	homozygous	128929054
11	82966560	82966561	G	A	18	GENIC	homozygous	115923137
11	82967873	82967874	G		6	GENIC	homozygous	128929056
11	82970727	82970729	GC		20	GENIC	homozygous	128929057
11	82970740	82970741	C		19	GENIC	homozygous	128929058
11	82970743	82970744	C		19	GENIC	homozygous	128929059
11	82970747	82970748	C	G	16	GENIC	homozygous	118166776
11	82970769	82970770	C		15	GENIC	homozygous	128929060
11	82970778	82970779	T	G	16	GENIC	homozygous	116223911
11	82970779	82970780	G	C	16	GENIC	homozygous	116223913
11	82970784	82970785	C	G	16	GENIC	homozygous	118166777
11	82970794	82970797	GCT		17	GENIC	homozygous	128929061
11	82970808	82970809	G		16	GENIC	homozygous	128929062
11	82970811	82970812	C		16	GENIC	homozygous	128929063
11	82970819	82970820	C	A	16	GENIC	homozygous	123537023
11	82970820	82970821	A	G	16	GENIC	homozygous	123537024
11	82970830	82970831	C		16	GENIC	homozygous	128929064
11	82970832	82970833	C		17	GENIC	homozygous	128929065
11	82970836	82970837	A	G	17	GENIC	homozygous	116421599
11	82970840	82970841	T		18	GENIC	homozygous	128929066
11	82970842	82970843	T		19	GENIC	homozygous	128929067
11	82970852	82970853	C		19	GENIC	homozygous	128929068
11	82970856	82970857	G		20	GENIC	homozygous	128929069
11	82970866	82970866		A	20	GENIC	homozygous	128929070
11	82970874	82970875	C		20	GENIC	homozygous	128929071
11	82970878	82970879	A		21	GENIC	homozygous	128929072
11	82970893	82970893		C	22	GENIC	homozygous	128929073
11	82970899	82970899		T	25	GENIC	homozygous	128929074
11	82970938	82970939	C		23	GENIC	homozygous	128929075
11	82971009	82971010	A		25	GENIC	homozygous	128929076
11	82970859	82970860	C	G	20	GENIC	homozygous	115996883