chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230303030	230303031	C	A	28	GENIC	homozygous	59431654
2	230304195	230304196	G	GA	11	GENIC	homozygous	59431656
2	230304206	230304207	G	GAAAAAAAAAAA	16	GENIC	heterozygous	60520629
2	230304700	230304701	A	G	25	GENIC	homozygous	59431657
2	230304748	230304749	G	A	27	GENIC	homozygous	59431658
2	230305092	230305093	C	T	34	GENIC	homozygous	59431659
2	230305972	230305973	C	A	33	GENIC	homozygous	59431660
2	230306206	230306207	T	C	37	GENIC	homozygous	59431661
2	230306284	230306285	A	G	24	GENIC	homozygous	59431662
2	230306356	230306357	G	GAA	18	GENIC	possibly homozygous	59431663
2	230307158	230307159	A	G	44	GENIC	homozygous	59431664
2	230307400	230307401	A	G	27	GENIC	homozygous	59431665
2	230307530	230307531	A	T	28	GENIC	homozygous	59431666
2	230307564	230307565	C	CG	17	GENIC	homozygous	59431667
2	230307630	230307636	TGGGGA	------	10	GENIC	heterozygous	60550442
2	230307714	230307715	C	T	28	GENIC	possibly homozygous	59431668