chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40518598	40518599	T	C	51	GENIC	possibly homozygous	52593154
8	40518628	40518629	A	G	50	GENIC	homozygous	52964367
8	40518631	40518632	G	C	51	GENIC	homozygous	52593155
8	40518635	40518636	A	C	48	GENIC	homozygous	52593156
8	40518656	40518657	T	C	50	GENIC	heterozygous	52593157
8	40518688	40518689	T	C	67	GENIC	heterozygous	52593158
8	40518694	40518695	C	A	73	GENIC	heterozygous	52593159
8	40518697	40518698	G	A	78	GENIC	heterozygous	52593160
8	40518700	40518701	T	C	85	GENIC	heterozygous	52593161
8	40518701	40518702	A	G	84	GENIC	heterozygous	52593162
8	40518717	40518718	A	G	101	GENIC	heterozygous	52964368
8	40518745	40518746	C	T	155	GENIC	heterozygous	52964369
8	40518760	40518761	T	C	173	GENIC	heterozygous	52593164
8	40518795	40518796	C	T	166	GENIC	heterozygous	52964370
8	40518839	40518840	C	T	118	GENIC	heterozygous	52964371
8	40518847	40518848	G	A	111	GENIC	heterozygous	52593166
8	40518857	40518858	C	-	60	GENIC	heterozygous	52964372
8	40518877	40518878	T	C	83	GENIC	heterozygous	52964373
8	40518898	40518899	C	T	84	GENIC	heterozygous	52593169
8	40519063	40519064	T	C	57	GENIC	homozygous	52593171
8	40519279	40519280	C	G	50	GENIC	possibly homozygous	52964374
8	40519372	40519373	A	T	53	GENIC	homozygous	52964375