chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	92560743	92560744	A	C	12	GENIC	homozygous	117198314
10	92560749	92560752	CTG		12	GENIC	homozygous	128845807
10	92560773	92560774	G		10	GENIC	homozygous	128845808
10	92560784	92560785	A		9	GENIC	homozygous	128845809
10	92560919	92560920	A		18	GENIC	homozygous	128845810
10	92560936	92560937	A		18	GENIC	homozygous	128845811
10	92560946	92560947	A		15	GENIC	homozygous	128845812
10	92560953	92560954	A		16	GENIC	homozygous	128845813
10	92560962	92560964	TA		15	GENIC	homozygous	128845814
10	92560975	92560976	A	G	16	GENIC	homozygous	117346861
10	92560978	92560979	G		16	GENIC	homozygous	128845815
10	92560988	92560989	T		16	GENIC	homozygous	128845816
10	92561003	92561003		A	17	GENIC	homozygous	128845817
10	92561012	92561013	T		17	GENIC	homozygous	128845818
10	92561025	92561025		A	19	GENIC	homozygous	128845819
10	92561241	92561242	G	T	10	GENIC	homozygous	118008346
10	92596845	92596846	G	T	20	GENIC	homozygous	116680846
10	92596867	92596868	A		17	GENIC	homozygous	128845865
10	92596903	92596904	C	A	17	GENIC	homozygous	116680848
10	92596904	92596905	T	C	17	GENIC	homozygous	116680850
10	92596926	92596927	G	C	19	GENIC	homozygous	116680852
10	92585515	92585516	A		17	GENIC	heterozygous	130577356