chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41342679	41342680	C	T	20	GENIC	homozygous	115329968
12	41345020	41345021	A	G	14	GENIC	homozygous	115329970
12	41347830	41347831	G	T	29	GENIC	homozygous	115329972
12	41348634	41348635	C	A	40	GENIC	homozygous	115329974
12	41353097	41353098	G	A	22	GENIC	homozygous	115329976
12	41353939	41353940	T	C	27	GENIC	homozygous	115329978
12	41355061	41355062	G	A	18	GENIC	homozygous	115329982
12	41357151	41357152	G	A	9	GENIC	homozygous	115329984
12	41357195	41357196	G	C	14	GENIC	homozygous	115385141
12	41357198	41357199	T	C	14	GENIC	homozygous	115329986
12	41357205	41357206	A	G	15	GENIC	homozygous	115329988
12	41357574	41357575	T	C	24	GENIC	homozygous	115329990
12	41357656	41357657	T	C	18	GENIC	homozygous	115385143
12	41357721	41357722	G	A	22	GENIC	homozygous	115329992
12	41357791	41357792	A	G	20	GENIC	homozygous	115329994
12	41357934	41357935	C	T	17	GENIC	homozygous	115329996
12	41360518	41360519	G	T	20	GENIC	homozygous	115329998
12	41361749	41361750	A	C	24	GENIC	homozygous	115330000