chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94312156	94312157	A	C	13	GENIC	homozygous	117605057
9	94312340	94312341	C	T	19	GENIC	homozygous	117605059
9	94312404	94312405	A	G	19	GENIC	homozygous	117605061
9	94312616	94312617	G	A	7	GENIC	homozygous	117390293
9	94313887	94313888	T	C	15	GENIC	homozygous	117605063
9	94315069	94315070	G	C	18	GENIC	homozygous	117605065
9	94315190	94315191	T	C	6	GENIC	homozygous	117605067
9	94317813	94317814	G	A	16	GENIC	homozygous	117605069
9	94318237	94318238	T	A	10	GENIC	homozygous	117605071
9	94319248	94319249	A	T	9	GENIC	homozygous	117605073
9	94319534	94319535	A	G	25	GENIC	homozygous	117605075
9	94320490	94320491	G	A	17	GENIC	homozygous	117605077
9	94320669	94320670	G	T	8	GENIC	homozygous	117605079
9	94320837	94320838	G	A	28	GENIC	homozygous	117605081
9	94321096	94321097	T	C	7	GENIC	homozygous	117390316
9	94321870	94321871	T	C	12	GENIC	homozygous	117605085
9	94321873	94321874	A	G	11	GENIC	homozygous	117605087
9	94323815	94323816	A	G	7	GENIC	homozygous	117390321
9	94324776	94324777	C	T	16	GENIC	homozygous	117605089
9	94324867	94324868	T	G	34	GENIC	homozygous	117605091