chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	72912593	72912593		T	28	GENIC	homozygous	128830110
10	72912600	72912600		A	26	GENIC	homozygous	128830111
10	72912620	72912621	T		21	GENIC	homozygous	128830112
10	72912627	72912627		T	19	GENIC	homozygous	128830113
10	72912663	72912663		G	11	GENIC	homozygous	128830114
10	72912722	72912723	T		41	GENIC	homozygous	128830115
10	72912730	72912731	A	T	43	GENIC	homozygous	116800098
10	72912762	72912763	A		41	GENIC	homozygous	128830116
10	72912780	72912781	T		35	GENIC	homozygous	128830117
10	72912781	72912782	C	G	35	GENIC	homozygous	116633284
10	72912786	72912787	A	C	35	GENIC	homozygous	116633286
10	72912800	72912800		TG	33	GENIC	homozygous	128830118
10	72912867	72912867		T	19	GENIC	homozygous	128830122
10	72912808	72912809	A		32	GENIC	homozygous	128830119
10	72912814	72912814		T	32	GENIC	homozygous	128830120
10	72912837	72912838	T		29	GENIC	homozygous	128830121
10	72912887	72912887		A	18	GENIC	homozygous	128830123
10	72912904	72912905	G	T	14	GENIC	possibly homozygous	117312983
10	72912905	72912906	C	G	14	GENIC	possibly homozygous	117312985
10	72912936	72912936		C	18	GENIC	homozygous	128830124
10	72918248	72918249	G		45	GENIC	homozygous	128830128