chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	81150785	81150786	C	T	34	GENIC	homozygous	55492658
5	81151510	81151511	C	CTGTATGG	18	GENIC	homozygous	55492660
5	81152765	81152766	T	C	24	GENIC	homozygous	55492662
5	81153077	81153078	C	A	22	GENIC	homozygous	55492664
5	81154508	81154509	G	A	17	GENIC	homozygous	55492666
5	81155187	81155188	A	G	35	GENIC	homozygous	55492668
5	81155608	81155609	A	G	31	GENIC	homozygous	55492670
5	81156672	81156673	A	G	30	GENIC	homozygous	55492672
5	81158316	81158317	C	T	25	GENIC	homozygous	55492674
5	81158685	81158686	C	A	34	GENIC	homozygous	55492676
5	81158707	81158711	CTTG	----	38	GENIC	homozygous	55492678
5	81159234	81159235	A	C	18	GENIC	homozygous	55492680
5	81159619	81159620	C	T	22	GENIC	homozygous	55492682
5	81160859	81160889	AAACCAAACCAAACCAAACCAAACCAAACC	------------------------------	14	GENIC	homozygous	56428914
5	81161297	81161298	A	AT	10	GENIC	homozygous	55492688
5	81161660	81161661	A	G	15	GENIC	homozygous	55492690
5	81161711	81161712	C	CT	9	GENIC	possibly homozygous	55492692