chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	55108408	55108409	G	T	40	GENIC	possibly homozygous	58358732
3	55109046	55109047	G	C	41	GENIC	homozygous	57377088
3	55109343	55109344	G	A	39	GENIC	homozygous	58358734
3	55109539	55109540	T	C	29	GENIC	homozygous	58358736
3	55109798	55109799	C	A	35	GENIC	homozygous	58358738
3	55109871	55109872	A	G	26	GENIC	homozygous	58358740
3	55109934	55109935	G	-	17	GENIC	homozygous	57377089
3	55109935	55109936	C	-	13	GENIC	heterozygous	57377090
3	55109945	55109949	CACT	----	19	GENIC	homozygous	58358742
3	55109946	55109949	ACT	---	21	GENIC	possibly homozygous	58358744
3	55110081	55110082	T	C	57	GENIC	homozygous	58358746
3	55110150	55110151	A	G	39	GENIC	homozygous	58358748
3	55111271	55111272	A	C	45	GENIC	homozygous	58358750
3	55111706	55111707	C	T	48	GENIC	homozygous	58358752
3	55111880	55111881	G	A	43	GENIC	homozygous	58358754
3	55112020	55112021	A	T	38	GENIC	homozygous	58358756
3	55112055	55112056	T	TA	26	GENIC	homozygous	58358758
3	55112131	55112132	G	T	35	GENIC	homozygous	58358760
3	55112468	55112469	T	C	45	GENIC	homozygous	58358762
3	55112508	55112509	T	C	48	GENIC	homozygous	58358764
3	55112608	55112609	G	A	46	GENIC	homozygous	58358766
3	55113019	55113020	A	-	43	GENIC	homozygous	58358768
3	55113276	55113277	A	T	56	GENIC	possibly homozygous	58358770
3	55113502	55113503	T	C	52	GENIC	homozygous	58358772
3	55113650	55113651	G	A	45	GENIC	possibly homozygous	58358774
3	55113669	55113670	G	C	45	GENIC	possibly homozygous	58358776
3	55114900	55114901	A	-	52	GENIC	homozygous	58358778
3	55115158	55115159	T	G	49	GENIC	possibly homozygous	58358780
3	55115398	55115399	T	A	53	GENIC	homozygous	58358782
3	55115774	55115775	A	G	36	GENIC	possibly homozygous	58358784
3	55117263	55117264	G	A	22	GENIC	homozygous	58358786