chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	34617199	34617200	T	C	22	GENIC	homozygous	52538104
9	34617436	34617437	C	G	39	GENIC	homozygous	52367457
9	34617910	34617911	A	G	35	GENIC	homozygous	52538106
9	34617937	34617938	C	A	41	GENIC	homozygous	52538108
9	34617979	34617980	A	T	30	GENIC	homozygous	52367461
9	34617992	34617993	C	T	29	GENIC	homozygous	52538110
9	34617995	34617996	T	A	29	GENIC	homozygous	52538112
9	34618098	34618099	A	G	41	GENIC	homozygous	52538114
9	34618118	34618119	T	C	48	GENIC	homozygous	51885340
9	34618142	34618143	A	G	44	GENIC	homozygous	52538116
9	34618411	34618412	G	C	41	GENIC	homozygous	52367467
9	34618690	34618691	G	A	29	GENIC	homozygous	52538118