chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	153515677	153515678	A	G	31	GENIC	homozygous	137654968
5	153515723	153515724	G	C	38	GENIC	homozygous	137654969
5	153515883	153515884	C	T	29	GENIC	homozygous	137654970
5	153515892	153515893	T	G	32	GENIC	homozygous	137654971
5	153516144	153516145	A	C	31	GENIC	homozygous	137654972
5	153516164	153516165	A	C	27	GENIC	homozygous	137654973
5	153516475	153516476	A	T	50	GENIC	homozygous	137654974
5	153516913	153516914	T	C	34	GENIC	homozygous	137654975
5	153516932	153516933	A	G	33	GENIC	homozygous	137654976
5	153517041	153517042	C	T	12	GENIC	homozygous	137654977
5	153517884	153517885	C	T	39	GENIC	homozygous	137654978
5	153517910	153517911	T	C	35	GENIC	homozygous	137654979
5	153519410	153519411	C	A	42	GENIC	possibly homozygous	137654980
5	153519657	153519658	C	G	50	GENIC	homozygous	137654981
5	153520188	153520189	C	T	41	GENIC	homozygous	137654982
5	153521634	153521635	A	T	50	GENIC	homozygous	137654983
5	153521663	153521664	G	A	51	GENIC	homozygous	137654984
5	153521693	153521694	A	G	49	GENIC	homozygous	137654985
5	153522163	153522164	A	G	48	GENIC	homozygous	137654986
5	153521358	153521359	T		18	GENIC	homozygous	137350050
5	153517519	153517523	AAAC		27	GENIC	possibly homozygous	137350048
5	153519625	153519627	CC		51	GENIC	homozygous	137350049