chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	92700097	92700098	G	A	52	GENIC	homozygous	120344007
9	92700285	92700286	C	T	45	GENIC	homozygous	120344008
9	92704862	92704864	AA		62	GENIC	homozygous	128732216
9	92707987	92707989	TG		36	GENIC	homozygous	128732218
9	92712495	92712495		C	51	GENIC	homozygous	128732219
9	92715092	92715092		C	31	GENIC	homozygous	128732220
9	92716145	92716146	C	G	42	GENIC	homozygous	117601634
9	92714361	92714362	A	G	54	GENIC	homozygous	117601626
9	92714481	92714482	A	G	45	GENIC	homozygous	117601628
9	92715982	92715983	A	G	50	GENIC	homozygous	117601632
9	92714116	92714116		TG	49	GENIC	homozygous	133836091
9	92716409	92716413	GTGC		25	GENIC	homozygous	133836092
9	92717208	92717212	GTGT		4	GENIC	homozygous	133836093
9	92717274	92717274		G	10	GENIC	homozygous	133836094
9	92717275	92717275		GTGCGTGCGTG	10	GENIC	homozygous	133836095
9	92717320	92717322	GT		16	GENIC	possibly homozygous	133836096
9	92717364	92717366	GT		25	GENIC	homozygous	128732222
9	92717571	92717571		C	44	GENIC	homozygous	128732223
9	92717669	92717670	G	A	44	GENIC	homozygous	120344009
9	92718217	92718218	G	A	59	GENIC	homozygous	120344010
9	92718270	92718271	A	G	51	GENIC	homozygous	117601636