chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	231882517	231882518	G	T	26	GENIC	homozygous	110303633
2	231889028	231889029	A	G	32	GENIC	homozygous	120175901
2	231890109	231890110	C	T	20	GENIC	homozygous	120175902
2	231890426	231890427	G	A	26	GENIC	homozygous	120175903
2	231894628	231894629	A	G	33	GENIC	homozygous	120175904
2	231894780	231894781	T	G	12	GENIC	homozygous	110303671
2	231900245	231900246	T	A	31	GENIC	homozygous	120175905
2	231904056	231904057	T	C	25	GENIC	homozygous	120175906
2	231907493	231907494	A	G	24	GENIC	homozygous	110303696
2	231909488	231909489	C	A	20	GENIC	homozygous	110303704
2	231910491	231910492	C	T	24	GENIC	homozygous	110303708
2	231912453	231912454	A	G	18	GENIC	homozygous	110303710
2	231915375	231915376	C	T	39	GENIC	homozygous	110303714
2	231920220	231920221	T	C	19	GENIC	homozygous	110303729
2	231921656	231921657	T	C	21	GENIC	heterozygous	120175907
2	231924065	231924066	C	T	20	GENIC	homozygous	110303754
2	231925928	231925929	G	A	28	GENIC	homozygous	120175908
2	231931191	231931192	T	A	8	GENIC	homozygous	110303812
2	231936907	231936908	G	A	19	GENIC	homozygous	110303852
2	231943532	231943533	A	T	33	GENIC	homozygous	110303921