chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	64482080	64482081	G	T	10	GENIC	homozygous	117043682
8	64482314	64482315	A	G	22	GENIC	possibly homozygous	117944623
8	64483392	64483393	T	C	39	GENIC	possibly homozygous	117043683
8	64483766	64483767	G	A	20	GENIC	homozygous	117043685
8	64485966	64485967	C	T	11	GENIC	homozygous	118023213
8	64487214	64487215	T	C	36	GENIC	possibly homozygous	117043689
8	64487219	64487220	A	G	39	GENIC	possibly homozygous	117043690
8	64487334	64487335	A	G	24	GENIC	homozygous	117043691
8	64488664	64488665	A	G	16	GENIC	possibly homozygous	118023215
8	64489029	64489030	T	C	23	GENIC	homozygous	117043692
8	64489344	64489345	A	G	43	GENIC	homozygous	117043693
8	64489390	64489391	C	T	43	GENIC	possibly homozygous	117043694
8	64490516	64490517	A	C	11	GENIC	homozygous	118023217
8	64490527	64490528	A	T	15	GENIC	homozygous	117043695
8	64491338	64491339	A	G	29	GENIC	homozygous	117043696
8	64491854	64491855	G	C	24	GENIC	homozygous	118023219
8	64495433	64495434	G	T	29	GENIC	homozygous	117043700
8	64495947	64495948	T	C	32	GENIC	possibly homozygous	117043702
8	64496697	64496698	G	C	32	GENIC	possibly homozygous	117043704
8	64497006	64497007	G	T	19	GENIC	homozygous	117043705
8	64497017	64497018	A	G	16	GENIC	homozygous	117043706
8	64497254	64497255	T	C	26	GENIC	homozygous	117043707
8	64497489	64497490	C	T	22	GENIC	homozygous	117944629
8	64501031	64501032	G	A	29	GENIC	homozygous	117043709
8	64501353	64501354	G	A	32	GENIC	homozygous	117944630
8	64502084	64502085	A	G	35	GENIC	homozygous	117043710