chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9730229	9730233	ACAG		11	GENIC	homozygous	131325161
3	9730789	9730790	A	G	19	GENIC	homozygous	112065355
3	9731842	9731843	T	C	16	GENIC	possibly homozygous	112065357
3	9732530	9732531	A	C	23	GENIC	homozygous	112065361
3	9732970	9732971	C	T	24	GENIC	homozygous	119966854
3	9731946	9731947	C	A	16	GENIC	homozygous	119966850
3	9732090	9732091	G	A	22	GENIC	homozygous	119966851
3	9732613	9732614	C	T	19	GENIC	homozygous	119966852
3	9732725	9732726	T	C	23	GENIC	homozygous	119966853
3	9732973	9732974	G	A	24	GENIC	homozygous	119966855
3	9733097	9733098	G	A	21	GENIC	homozygous	119966856
3	9733292	9733293	G	A	12	GENIC	homozygous	119966857
3	9733483	9733484	C	G	14	GENIC	homozygous	119966858
3	9733488	9733488		TG	16	GENIC	homozygous	131325162
3	9733699	9733700	G	A	20	GENIC	homozygous	119966859
3	9734218	9734219	C	T	22	GENIC	homozygous	112065371
3	9734308	9734309	T	C	20	GENIC	homozygous	112065373
3	9734504	9734505	A	G	11	GENIC	homozygous	112065375
3	9734627	9734628	A	G	18	GENIC	homozygous	112065377
3	9734874	9734875	G	A	14	GENIC	homozygous	112065379
3	9735071	9735072	A	G	17	GENIC	homozygous	112065381
3	9735317	9735318	A	C	17	GENIC	possibly homozygous	119966860
3	9735339	9735339		AAAC	13	GENIC	homozygous	131325163
3	9735709	9735710	T	A	18	GENIC	homozygous	112065385
3	9735921	9735921		T	17	GENIC	homozygous	131325164
3	9736187	9736188	T	C	17	GENIC	homozygous	112065387
3	9736739	9736740	C	T	19	GENIC	homozygous	119966861
3	9736889	9736890	C	T	22	GENIC	homozygous	119966862
3	9737759	9737760	G	A	30	GENIC	homozygous	119966863
3	9738022	9738023	G	A	19	GENIC	homozygous	119966864
3	9738041	9738042	G	C	17	GENIC	possibly homozygous	112065391
3	9738149	9738150	A	G	20	GENIC	homozygous	112065395
3	9738736	9738737	G	C	10	GENIC	heterozygous	112223430