chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	97866254	97866255	T	TAA	5	GENIC	homozygous	58319884
3	97866353	97866354	A	T	4	GENIC	homozygous	57571068
3	97866364	97866365	T	A	6	GENIC	homozygous	57571070
3	97867508	97867509	A	G	9	GENIC	homozygous	57571074
3	97867542	97867543	T	G	30	GENIC	heterozygous	57571076
3	97867865	97867866	G	A	19	GENIC	heterozygous	57571078
3	97867928	97867929	T	C	19	GENIC	heterozygous	57571080
3	97868020	97868021	T	C	15	GENIC	homozygous	57571082
3	97868037	97868038	T	TA	12	GENIC	homozygous	57571084
3	97868680	97868681	A	C	19	GENIC	heterozygous	57571088
3	97869211	97869212	A	G	22	GENIC	possibly homozygous	57571092
3	97869274	97869275	T	TG	14	GENIC	homozygous	57571094
3	97869604	97869605	C	T	24	GENIC	homozygous	57571096
3	97869802	97869803	C	T	13	GENIC	homozygous	57571098
3	97870597	97870598	T	G	17	GENIC	homozygous	57571100
3	97870964	97870965	A	G	18	GENIC	homozygous	57571102
3	97871110	97871111	G	A	11	GENIC	heterozygous	58319885
3	97871461	97871462	G	A	17	GENIC	homozygous	58319886
3	97871478	97871479	G	C	11	GENIC	homozygous	57571104
3	97873072	97873073	C	T	9	GENIC	homozygous	57571112
3	97874975	97874976	T	C	20	GENIC	homozygous	58319887