chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	92838901	92838902	C	CT	4	GENIC	homozygous	52279045
9	92839501	92839502	G	GT	31	GENIC	possibly homozygous	52664115
9	92840905	92840906	C	T	18	GENIC	homozygous	52664119
9	92841144	92841145	A	AT	10	GENIC	possibly homozygous	52664121
9	92842572	92842573	A	AT	9	GENIC	possibly homozygous	52664123
9	92843457	92843458	A	G	35	GENIC	homozygous	52047064
9	92843502	92843503	G	A	35	GENIC	homozygous	52664125
9	92844338	92844339	T	C	18	GENIC	homozygous	52664127
9	92844374	92844375	T	-	9	GENIC	possibly homozygous	52047072
9	92848453	92848454	T	G	31	GENIC	possibly homozygous	52664129
9	92849691	92849692	A	AT	13	GENIC	heterozygous	52047122
9	92849928	92849929	T	C	15	GENIC	homozygous	52664131
9	92850548	92850551	AAA	---	16	GENIC	heterozygous	52047132
9	92850549	92850551	AA	--	16	GENIC	heterozygous	52047134
9	92851922	92851923	G	A	21	GENIC	possibly homozygous	52664133
9	92852549	92852550	G	GT	25	GENIC	homozygous	52664135
9	92854841	92854842	A	-	30	GENIC	possibly homozygous	52476541
9	92850550	92850551	A	-	16	GENIC	heterozygous	52955185