chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94310608	94310609	T	C	6	GENIC	homozygous	117602015
9	94311468	94311469	C	A	72	GENIC	homozygous	117602017
9	94311758	94311759	G	A	57	GENIC	possibly homozygous	117602019
9	94312001	94312002	G	C	57	GENIC	homozygous	117602021
9	94312156	94312157	A	C	55	GENIC	homozygous	117390288
9	94312404	94312405	A	G	64	GENIC	homozygous	117390292
9	94312448	94312449	G	A	74	GENIC	homozygous	117602023
9	94313068	94313069	C	T	64	GENIC	homozygous	117602025
9	94314693	94314694	G	A	86	GENIC	possibly homozygous	117602027
9	94316650	94316651	A	G	74	GENIC	homozygous	117602029
9	94317900	94317901	T	C	46	GENIC	homozygous	117602031
9	94319498	94319499	C	T	68	GENIC	homozygous	117602033
9	94319534	94319535	A	G	78	GENIC	homozygous	117390306
9	94320837	94320838	G	A	52	GENIC	homozygous	117390311
9	94321122	94321123	C	G	53	GENIC	heterozygous	117602035
9	94321870	94321871	T	C	50	GENIC	homozygous	117390318
9	94321873	94321874	A	G	49	GENIC	homozygous	117390319
9	94322064	94322065	G	T	60	GENIC	heterozygous	117390320
9	94323987	94323988	T	C	48	GENIC	heterozygous	117390323
9	94324867	94324868	T	G	50	GENIC	homozygous	117390327