chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	146643951	146643952	T		12	GENIC	homozygous	130283821
3	146643953	146644080	GAGGAGGAGGAGGGAGAGGAGGAGGAGGAGGAGGAGAAGAGGAGGAAGAAGAGGAGGAGGAAGAAGAGGAGGAGGAAGAGGATGAGGAAGAGGAGGAGGAAGAGGAGGAGGAAGAGGAGGAGGAGGT		14	GENIC	possibly homozygous	130283822
3	146650734	146650735	T	A	49	GENIC	homozygous	119685916
3	146650763	146650765	AC		45	GENIC	homozygous	127939748
3	146650733	146650733		T	48	GENIC	homozygous	127939746
3	146650751	146650752	C		41	GENIC	homozygous	127939747
3	146650811	146650812	A		39	GENIC	homozygous	127939749
3	146650816	146650816		AT	40	GENIC	homozygous	127939750
3	146650857	146650859	TT		59	GENIC	homozygous	127939751
3	146650864	146650864		GAG	59	GENIC	homozygous	127939752
3	146650867	146650868	G		61	GENIC	homozygous	127939753
3	146650873	146650873		T	61	GENIC	homozygous	127939754
3	146650926	146650927	A		54	GENIC	homozygous	127939755
3	146664509	146664512	TCA		18	GENIC	heterozygous	130283823
3	146664540	146664541	A	G	22	GENIC	homozygous	112257164
3	146664547	146664548	A	G	24	GENIC	homozygous	112257165
3	146664567	146664568	A	C	23	GENIC	homozygous	112035299
3	146664573	146664574	T	C	25	GENIC	homozygous	112035301
3	146664597	146664598	A		29	GENIC	homozygous	127939756
3	146664598	146664599	G	C	29	GENIC	homozygous	127993943
3	146650820	146650821	G	C	43	GENIC	homozygous	111767734
3	146664515	146664516	G	T	21	GENIC	homozygous	111767738
3	146650859	146650860	G	C	59	GENIC	homozygous	119652164
3	146664578	146664579	A	C	28	GENIC	homozygous	127993941
3	146664579	146664580	G	A	27	GENIC	homozygous	127993942
3	146664604	146664605	G	C	30	GENIC	homozygous	127993944
3	146664604	146664604		C	29	GENIC	homozygous	127939757
3	146672437	146672438	A	C	44	GENIC	homozygous	111767742
3	146681653	146681653		A	63	GENIC	possibly homozygous	127939758
3	146681904	146681906	AA		52	GENIC	homozygous	127939759
3	146681910	146681911	C		52	GENIC	homozygous	127939760
3	146676936	146676937	A	G	68	GENIC	homozygous	130291928