chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	128610508	128610509	T	C	72	GENIC	homozygous	116721755
8	128612788	128612789	G	T	59	GENIC	homozygous	116721756
8	128612804	128612805	A	T	56	GENIC	homozygous	116721757
8	128612964	128612965	T	C	47	GENIC	homozygous	116721758
8	128614124	128614125	T	C	44	GENIC	homozygous	116721759
8	128614374	128614375	T	C	34	GENIC	homozygous	116721760
8	128614642	128614643	A	G	53	GENIC	homozygous	116721761
8	128614688	128614689	T	C	52	GENIC	homozygous	116721762
8	128615024	128615025	C	T	51	GENIC	homozygous	116721763
8	128615031	128615032	C	G	54	GENIC	homozygous	116721764
8	128615296	128615297	G	A	51	GENIC	homozygous	116721765
8	128615754	128615755	C	A	47	GENIC	possibly homozygous	116721766
8	128616071	128616072	T	C	52	GENIC	homozygous	116721767
8	128616088	128616089	G	A	50	GENIC	homozygous	116721768
8	128617030	128617031	C	T	30	GENIC	heterozygous	116721769
8	128617379	128617380	T	C	46	GENIC	possibly homozygous	116721770
8	128617961	128617962	C	T	54	GENIC	homozygous	116721771
8	128618091	128618092	G	A	57	GENIC	homozygous	116721772
8	128618402	128618403	G	A	53	GENIC	homozygous	116721773
8	128618425	128618426	A	T	56	GENIC	homozygous	116721774
8	128619575	128619576	C	T	49	GENIC	homozygous	116721775
8	128619585	128619586	T	C	54	GENIC	homozygous	116721776
8	128619748	128619749	C	T	48	GENIC	homozygous	116721777
8	128619772	128619773	G	A	49	GENIC	homozygous	116721778
8	128620552	128620553	A	G	55	GENIC	heterozygous	116901697