chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	97866353	97866354	A	T	37	GENIC	heterozygous	57571068
3	97866364	97866365	T	A	37	GENIC	heterozygous	57571070
3	97866620	97866621	C	T	25	GENIC	heterozygous	57571072
3	97867508	97867509	A	G	32	GENIC	heterozygous	57571074
3	97867542	97867543	T	G	29	GENIC	heterozygous	57571076
3	97867865	97867866	G	A	32	GENIC	heterozygous	57571078
3	97867928	97867929	T	C	41	GENIC	heterozygous	57571080
3	97868020	97868021	T	C	44	GENIC	heterozygous	57571082
3	97868037	97868038	T	TA	44	GENIC	heterozygous	57571084
3	97868615	97868616	A	G	36	GENIC	heterozygous	57571086
3	97868680	97868681	A	C	26	GENIC	heterozygous	57571088
3	97868826	97868827	A	G	23	GENIC	heterozygous	57571090
3	97869211	97869212	A	G	24	GENIC	heterozygous	57571092
3	97869274	97869275	T	TG	36	GENIC	heterozygous	57571094
3	97869604	97869605	C	T	37	GENIC	heterozygous	57571096
3	97869802	97869803	C	T	19	GENIC	heterozygous	57571098
3	97870597	97870598	T	G	17	GENIC	heterozygous	57571100
3	97870964	97870965	A	G	19	GENIC	heterozygous	57571102
3	97871478	97871479	G	C	19	GENIC	heterozygous	57571104
3	97873001	97873002	A	G	45	GENIC	heterozygous	57571110
3	97873072	97873073	C	T	40	GENIC	heterozygous	57571112