chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	100991369	100991370	T	TC	20	GENIC	homozygous	57578739
3	101000762	101000763	T	TC	30	GENIC	homozygous	57578743
3	101002320	101002321	A	-	14	GENIC	heterozygous	57578745
3	101007541	101007542	A	AT	16	GENIC	heterozygous	58321565
3	101014510	101014512	AC	--	9	GENIC	heterozygous	57578747
3	101025271	101025272	A	-	5	GENIC	heterozygous	58168122
3	101029663	101029664	T	TA	5	GENIC	heterozygous	57933307
3	101029664	101029665	A	-	5	GENIC	heterozygous	57578749
3	101031193	101031194	T	TTG	15	GENIC	heterozygous	57578751
3	101031904	101031905	C	T	24	GENIC	homozygous	57578753
3	101031905	101031906	C	T	25	GENIC	homozygous	57578755
3	101031907	101031908	C	A	25	GENIC	homozygous	57578757
3	101035164	101035165	A	AAC	11	GENIC	possibly homozygous	57578761
3	101039074	101039075	C	CTTA	22	GENIC	homozygous	57578763
3	101039295	101039296	G	T	20	GENIC	homozygous	57578765
3	101039298	101039299	G	A	19	GENIC	homozygous	57578767
3	101039308	101039309	T	C	23	GENIC	homozygous	57578773
3	101039312	101039313	T	C	23	GENIC	homozygous	57578775
3	101039319	101039320	T	C	23	GENIC	homozygous	57578777
3	101039335	101039336	T	G	22	GENIC	homozygous	57578779
3	101046982	101046984	GG	--	7	GENIC	homozygous	57578785
3	101049448	101049449	A	-	7	GENIC	heterozygous	57578791
3	101051311	101051312	G	A	6	GENIC	heterozygous	57933367
3	101051344	101051345	G	C	8	GENIC	heterozygous	57578793
3	101051354	101051355	C	G	10	GENIC	heterozygous	57578795
3	101051381	101051382	C	-	10	GENIC	homozygous	57578797
3	101051385	101051387	CG	--	10	GENIC	homozygous	57578799
3	101051387	101051388	C	-	9	GENIC	homozygous	57578801
3	101053740	101053741	A	-	7	GENIC	possibly homozygous	57578803