chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	81150785	81150786	C	T	64	GENIC	homozygous	55492658
5	81151510	81151511	C	CTGTATGG	19	GENIC	homozygous	55492660
5	81152765	81152766	T	C	44	GENIC	homozygous	55492662
5	81153077	81153078	C	A	39	GENIC	possibly homozygous	55492664
5	81154508	81154509	G	A	37	GENIC	possibly homozygous	55492666
5	81155187	81155188	A	G	30	GENIC	homozygous	55492668
5	81155608	81155609	A	G	45	GENIC	possibly homozygous	55492670
5	81156672	81156673	A	G	69	GENIC	homozygous	55492672
5	81158316	81158317	C	T	56	GENIC	homozygous	55492674
5	81158685	81158686	C	A	38	GENIC	possibly homozygous	55492676
5	81158707	81158711	CTTG	----	33	GENIC	homozygous	55492678
5	81159234	81159235	A	C	39	GENIC	homozygous	55492680
5	81159619	81159620	C	T	44	GENIC	homozygous	55492682
5	81160886	81160889	ACC	---	16	GENIC	homozygous	55492684
5	81160887	81160888	C	CA	14	GENIC	possibly homozygous	55492686
5	81161297	81161298	A	AT	16	GENIC	possibly homozygous	55492688
5	81161660	81161661	A	G	40	GENIC	homozygous	55492690
5	81161711	81161712	C	CT	15	GENIC	heterozygous	55492692