chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	211051300	211051301	T	A	44	GENIC	homozygous	110223961
2	211053662	211053663	C	T	49	GENIC	homozygous	110223963
2	211053850	211053851	A	G	52	GENIC	homozygous	110223964
2	211053690	211053691	G	A	53	GENIC	homozygous	111363810
2	211055096	211055097	C	A	23	GENIC	possibly homozygous	111363812
2	211055618	211055619	T	G	53	GENIC	homozygous	111363814
2	211057165	211057166	G	T	30	GENIC	homozygous	111363816
2	211059092	211059093	G	A	54	GENIC	homozygous	110223975
2	211061401	211061402	G	T	56	GENIC	homozygous	110223978
2	211061818	211061819	G	A	44	GENIC	homozygous	111363818
2	211062131	211062132	A	G	18	GENIC	possibly homozygous	110223981
2	211062175	211062176	C	A	15	GENIC	heterozygous	111363820
2	211062270	211062271	A	G	51	GENIC	homozygous	110223984
2	211065289	211065290	C	T	57	GENIC	possibly homozygous	110223988
2	211065386	211065387	A	T	22	GENIC	homozygous	110223989
2	211069089	211069090	T	C	59	GENIC	homozygous	110223992
2	211069684	211069685	T	C	25	GENIC	homozygous	110223993
2	211071618	211071619	C	T	66	GENIC	possibly homozygous	111363822
2	211072300	211072301	A	T	39	GENIC	homozygous	111363824
2	211072468	211072469	C	T	50	GENIC	homozygous	110224001
2	211073003	211073004	A	G	36	GENIC	possibly homozygous	110224004
2	211073025	211073026	C	T	39	GENIC	heterozygous	111363826