chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	94311468	94311469	C	A	35	GENIC	homozygous	117602017
9	94311758	94311759	G	A	17	GENIC	homozygous	117602019
9	94312001	94312002	G	C	19	GENIC	homozygous	117602021
9	94312156	94312157	A	C	23	GENIC	homozygous	117390288
9	94312404	94312405	A	G	29	GENIC	homozygous	117390292
9	94312448	94312449	G	A	23	GENIC	homozygous	117602023
9	94313068	94313069	C	T	31	GENIC	homozygous	117602025
9	94314693	94314694	G	A	17	GENIC	homozygous	117602027
9	94316650	94316651	A	G	28	GENIC	homozygous	117602029
9	94317900	94317901	T	C	25	GENIC	homozygous	117602031
9	94319534	94319535	A	G	31	GENIC	homozygous	117390306
9	94320837	94320838	G	A	14	GENIC	homozygous	117390311
9	94321096	94321097	T	C	2	GENIC	homozygous	117390316
9	94321870	94321871	T	C	24	GENIC	homozygous	117390318
9	94321873	94321874	A	G	24	GENIC	homozygous	117390319
9	94324867	94324868	T	G	14	GENIC	homozygous	117390327