chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	96551769	96551770	C	G	47	GENIC	homozygous	116589658
8	96551885	96551886	G	A	43	GENIC	homozygous	116589660
8	96552201	96552202	T	C	38	GENIC	homozygous	116589664
8	96552421	96552422	G	C	49	GENIC	homozygous	116589666
8	96552966	96552967	T	G	44	GENIC	homozygous	116589668
8	96553528	96553529	T	C	48	GENIC	homozygous	116589670
8	96553566	96553567	G	A	48	GENIC	homozygous	116589672
8	96553852	96553853	T	C	46	GENIC	homozygous	116589674
8	96554544	96554545	A	G	39	GENIC	homozygous	116589676
8	96555336	96555337	T	G	37	GENIC	homozygous	116589678
8	96555760	96555761	C	T	57	GENIC	homozygous	116589680
8	96556018	96556019	C	T	53	GENIC	homozygous	116589682
8	96556678	96556679	T	C	59	GENIC	homozygous	116589684
8	96551899	96551899		TTTG	44	GENIC	homozygous	128618139
8	96551911	96551911		TTTTTG	40	GENIC	homozygous	128618140
8	96552087	96552088	T		45	GENIC	homozygous	128618141
8	96554077	96554077		T	43	GENIC	homozygous	128618142
8	96554915	96554915		TCACGGAAA	30	GENIC	homozygous	128618143
8	96557635	96557636	G	A	49	GENIC	homozygous	116589686
8	96558132	96558133	T	C	37	GENIC	homozygous	116589688