chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	210394186	210394187	G	C	51	GENIC	homozygous	110223085
2	210395945	210395946	T	C	50	GENIC	homozygous	110223086
2	210400899	210400900	A	G	46	GENIC	homozygous	110223088
2	210402120	210402121	A	G	45	GENIC	homozygous	110223089
2	210404084	210404085	T	C	41	GENIC	homozygous	110223090
2	210400339	210400339		C	15	GENIC	homozygous	127732589
2	210404542	210404543	T		39	GENIC	homozygous	127732590
2	210404690	210404691	G	A	47	GENIC	homozygous	110223091
2	210406992	210406993	A	G	51	GENIC	possibly homozygous	110223092
2	210408095	210408096	G	A	52	GENIC	homozygous	110223093
2	210410268	210410269	G	A	42	GENIC	homozygous	110223094
2	210411408	210411409	T	C	58	GENIC	homozygous	110223095
2	210411976	210411977	C	T	49	GENIC	homozygous	110223096
2	210412217	210412218	C	G	51	GENIC	homozygous	110223097
2	210413158	210413159	A	T	50	GENIC	homozygous	110223098
2	210413227	210413228	T	C	47	GENIC	homozygous	110223099
2	210413369	210413370	T	A	47	GENIC	homozygous	110223100