chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40518598	40518599	T	C	44	GENIC	homozygous	52593154
8	40518631	40518632	G	C	58	GENIC	homozygous	52593155
8	40518635	40518636	A	C	62	GENIC	homozygous	52593156
8	40518656	40518657	T	C	78	GENIC	heterozygous	52593157
8	40518688	40518689	T	C	102	GENIC	heterozygous	52593158
8	40518694	40518695	C	A	98	GENIC	heterozygous	52593159
8	40518697	40518698	G	A	102	GENIC	heterozygous	52593160
8	40518700	40518701	T	C	110	GENIC	heterozygous	52593161
8	40518701	40518702	A	G	111	GENIC	heterozygous	52593162
8	40518721	40518722	T	G	128	GENIC	heterozygous	52593163
8	40518760	40518761	T	C	176	GENIC	heterozygous	52593164
8	40518838	40518839	T	C	79	GENIC	heterozygous	52593165
8	40518847	40518848	G	A	69	GENIC	heterozygous	52593166
8	40518893	40518894	T	A	35	GENIC	heterozygous	52593167
8	40518895	40518896	T	C	34	GENIC	possibly homozygous	52593168
8	40518898	40518899	C	T	35	GENIC	heterozygous	52593169
8	40518902	40518903	C	T	34	GENIC	homozygous	52593170
8	40519063	40519064	T	C	46	GENIC	possibly homozygous	52593171