chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89105134	89105135	G	A	42	GENIC	possibly homozygous	116675076
10	89107690	89107691	T	A	33	GENIC	homozygous	116675078
10	89107932	89107933	G	A	41	GENIC	homozygous	116675080
10	89109739	89109740	T	C	60	GENIC	homozygous	116675082
10	89112468	89112469	G	T	58	GENIC	homozygous	116902182
10	89116937	89116938	C	T	34	GENIC	homozygous	116675096
10	89116949	89116950	A	G	32	GENIC	homozygous	116675098
10	89118856	89118857	A	G	31	GENIC	possibly homozygous	117197721
10	89121809	89121810	A	G	68	GENIC	possibly homozygous	116675102
10	89123079	89123080	C	T	79	GENIC	possibly homozygous	116902184
10	89123146	89123147	G	A	54	GENIC	homozygous	116902186
10	89124297	89124298	G	C	50	GENIC	homozygous	116675106
10	89124581	89124582	G	C	46	GENIC	homozygous	116675108
10	89125820	89125821	T	C	73	GENIC	possibly homozygous	116675110
10	89127412	89127413	A	G	69	GENIC	homozygous	116675112
10	89127461	89127462	A	G	75	GENIC	homozygous	116675114
10	89128621	89128622	G	T	66	GENIC	homozygous	116902188
10	89130531	89130532	G	A	50	GENIC	possibly homozygous	116902190
10	89130550	89130551	T	C	42	GENIC	homozygous	116675118
10	89130764	89130765	T	C	52	GENIC	homozygous	116675120
10	89130808	89130809	T	A	52	GENIC	homozygous	116902192
10	89131551	89131552	A	C	56	GENIC	possibly homozygous	116675122
10	89132622	89132623	A	G	53	GENIC	homozygous	116675124
10	89132749	89132750	A	G	66	GENIC	homozygous	116675126
10	89133423	89133424	T	C	66	GENIC	homozygous	116902194
10	89133749	89133750	G	A	64	GENIC	homozygous	116902196
10	89134707	89134708	G	C	79	GENIC	homozygous	117087251
10	89136494	89136495	A	C	57	GENIC	homozygous	116902198
10	89137452	89137453	T	A	46	GENIC	possibly homozygous	118048806
10	89134434	89134435	C	G	67	GENIC	heterozygous	118048804
10	89134511	89134512	A	T	78	GENIC	heterozygous	118048805
10	89137489	89137490	C	T	36	GENIC	possibly homozygous	117227883