chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230214243	230214244	G	A	5	GENIC	homozygous	74441118
2	230215819	230215820	T	C	18	GENIC	homozygous	74441120
2	230216246	230216247	C	T	25	GENIC	homozygous	74441122
2	230216456	230216456		G	6	GENIC	homozygous	75856758
2	230216833	230216834	C	T	26	GENIC	homozygous	74441124
2	230218887	230218888	T	C	13	GENIC	homozygous	74441128
2	230219183	230219184	A	C	10	GENIC	homozygous	74441130
2	230219448	230219449	A	G	6	GENIC	homozygous	74441132
2	230220848	230220849	A	G	11	GENIC	homozygous	74441136
2	230221686	230221687	T	C	17	GENIC	homozygous	74441138
2	230221863	230221864	C	T	13	GENIC	homozygous	74441140
2	230225666	230225667	A	G	14	GENIC	homozygous	75856760
2	230225714	230225715	G	A	21	GENIC	homozygous	74441142
2	230226709	230226710	T	C	6	GENIC	homozygous	74441144
2	230227326	230227327	G	C	32	GENIC	homozygous	74441146
2	230228349	230228350	T	C	28	GENIC	homozygous	74441148
2	230228839	230228840	A	T	21	GENIC	homozygous	74441154
2	230229653	230229654	A		10	GENIC	heterozygous	75856762
2	230229843	230229843		A	22	GENIC	homozygous	75856764
2	230230198	230230199	G	T	10	GENIC	homozygous	74441158
2	230230434	230230435	G	A	16	GENIC	homozygous	74441160