chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	97866353	97866354	A	T	3	GENIC	heterozygous	57571068
3	97866364	97866365	T	A	3	GENIC	homozygous	57571070
3	97866620	97866621	C	T	14	GENIC	possibly homozygous	57571072
3	97867508	97867509	A	G	13	GENIC	homozygous	57571074
3	97867542	97867543	T	G	22	GENIC	possibly homozygous	57571076
3	97867865	97867866	G	A	13	GENIC	heterozygous	57571078
3	97867928	97867929	T	C	16	GENIC	heterozygous	57571080
3	97868020	97868021	T	C	14	GENIC	possibly homozygous	57571082
3	97868037	97868038	T	TA	12	GENIC	heterozygous	57571084
3	97868615	97868616	A	G	15	GENIC	homozygous	57571086
3	97868680	97868681	A	C	14	GENIC	homozygous	57571088
3	97868826	97868827	A	G	19	GENIC	homozygous	57571090
3	97869211	97869212	A	G	34	GENIC	possibly homozygous	57571092
3	97869274	97869275	T	TG	23	GENIC	homozygous	57571094
3	97869604	97869605	C	T	23	GENIC	possibly homozygous	57571096
3	97869802	97869803	C	T	23	GENIC	homozygous	57571098
3	97870597	97870598	T	G	31	GENIC	possibly homozygous	57571100
3	97870964	97870965	A	G	28	GENIC	homozygous	57571102
3	97871478	97871479	G	C	17	GENIC	possibly homozygous	57571104
3	97872677	97872678	C	A	9	GENIC	heterozygous	57571106
3	97872732	97872733	T	C	12	GENIC	heterozygous	57571108
3	97873001	97873002	A	G	12	GENIC	homozygous	57571110
3	97873072	97873073	C	T	17	GENIC	homozygous	57571112
3	97873885	97873886	T	C	13	GENIC	homozygous	57571114
3	97874174	97874175	A	C	16	GENIC	possibly homozygous	57571116
3	97874185	97874186	A	C	16	GENIC	possibly homozygous	57571118
3	97874993	97874994	G	A	17	GENIC	homozygous	57571120
3	97876742	97876746	GTTA	----	7	GENIC	homozygous	57571122