chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	228382752	228382753	A	G	11	GENIC	homozygous	109000662
1	228382813	228382814	C	T	15	GENIC	possibly homozygous	109000663
1	228383190	228383191	T	C	26	GENIC	possibly homozygous	109000664
1	228383552	228383553	A	G	24	GENIC	homozygous	109000665
1	228384922	228384923	G	A	23	GENIC	homozygous	109000667
1	228385584	228385585	C	T	20	GENIC	homozygous	109000668
1	228388359	228388360	G	A	22	GENIC	homozygous	109000672
1	228388602	228388603	G	T	31	GENIC	homozygous	109000673
1	228389734	228389735	C	T	25	GENIC	possibly homozygous	109000674
1	228390845	228390846	C	G	15	GENIC	homozygous	109000678
1	228391770	228391771	T	C	19	GENIC	homozygous	109000679
1	228392450	228392451	C	T	25	GENIC	homozygous	109000680
1	228392976	228392977	G	A	26	GENIC	homozygous	109000681
1	228393448	228393449	C	A	26	GENIC	homozygous	109000682
1	228394226	228394227	A	C	20	GENIC	homozygous	109000683
1	228394927	228394928	A	G	25	GENIC	homozygous	109000684
1	228387312	228387313	C	T	19	GENIC	homozygous	109057121
1	228387013	228387014	G	A	10	GENIC	homozygous	120515640