chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5611484	5611485	G	A	35	GENIC	homozygous	143717911
20	5612328	5612329	C	G	22	GENIC	homozygous	143717912
20	5612330	5612331	T	G	22	GENIC	homozygous	143717913
20	5614145	5614146	C	T	42	GENIC	homozygous	143717914
20	5614379	5614380	A	G	62	GENIC	homozygous	143717915
20	5614500	5614501	G	A	54	GENIC	homozygous	143717916
20	5614511	5614512	C	T	48	GENIC	homozygous	143717917
20	5614813	5614814	A	G	26	GENIC	homozygous	143717918
20	5614846	5614847	G	A	26	GENIC	homozygous	143717919
20	5615033	5615034	G	A	54	GENIC	homozygous	143717920
20	5615512	5615520	CCTGTGGC		29	GENIC	homozygous	129980274
20	5615624	5615625	C	A	48	GENIC	homozygous	143717921
20	5615641	5615642	T	C	54	GENIC	homozygous	143717922
20	5615648	5615649	C	G	57	GENIC	homozygous	143717923
20	5615709	5615712	TTA		53	GENIC	homozygous	143709920
20	5616571	5616572	C	T	27	GENIC	heterozygous	403680768
20	5616568	5616569	C		27	GENIC	heterozygous	403680765
20	5616568	5616569	C	G	27	GENIC	heterozygous	403680766
20	5616571	5616572	C		27	GENIC	heterozygous	403680767
20	5616572	5616573	C		27	GENIC	heterozygous	403680769
20	5616572	5616573	C	T	27	GENIC	heterozygous	403680770
20	5616646	5616647	C	T	40	GENIC	homozygous	143717924
20	5617335	5617336	T		19	GENIC	homozygous	129980275
20	5617360	5617363	CTC		32	GENIC	homozygous	129980276
20	5618360	5618361	C	T	47	GENIC	possibly homozygous	130036033
20	5618572	5618573	C		48	GENIC	homozygous	129980277