chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	147239199	147239200	G	A	46	GENIC	homozygous	112364703
3	147241708	147241709	A	G	44	GENIC	homozygous	112364709
3	147244254	147244254		A	61	GENIC	homozygous	134674753
3	147247762	147247763	A	C	50	GENIC	possibly homozygous	112364711
3	147248213	147248214	A	T	49	GENIC	homozygous	112364713
3	147248273	147248274	T	G	45	GENIC	homozygous	112364715
3	147248565	147248566	T	C	51	GENIC	homozygous	119652180
3	147248566	147248567	C	T	51	GENIC	homozygous	119652181
3	147249764	147249765	T	C	53	GENIC	homozygous	112364717
3	147253075	147253076	T	C	51	GENIC	homozygous	112364719
3	147253854	147253854		ACAT	29	GENIC	possibly homozygous	134674754
3	147255064	147255065	C	A	41	GENIC	homozygous	112364721
3	147255648	147255649	C	T	44	GENIC	homozygous	112364723
3	147255691	147255695	TGTC		42	GENIC	homozygous	134674755
3	147256308	147256309	T	C	29	GENIC	homozygous	112364725
3	147256432	147256432		C	12	GENIC	homozygous	134674756
3	147256444	147256445	A	C	14	GENIC	homozygous	112364727
3	147256446	147256447	A	C	14	GENIC	homozygous	112364729
3	147257139	147257147	GCGCGTGT		50	GENIC	homozygous	134674757
3	147257160	147257161	T	C	53	GENIC	homozygous	112364731
3	147257167	147257168	A	G	53	GENIC	homozygous	112364733
3	147257317	147257318	C	T	49	GENIC	possibly homozygous	112364735
3	147258687	147258688	T		53	GENIC	homozygous	134674758
3	147259865	147259866	T	C	50	GENIC	homozygous	112364737
3	147261145	147261145		T	39	GENIC	heterozygous	134674759
3	147248593	147248593		A	46	GENIC	homozygous	127940326
3	147260669	147260670	G	A	59	GENIC	homozygous	112364739