chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89105134	89105135	G	A	16	GENIC	possibly homozygous	116675076
10	89107690	89107691	T	A	25	GENIC	homozygous	116675078
10	89107932	89107933	G	A	24	GENIC	homozygous	116675080
10	89109739	89109740	T	C	26	GENIC	homozygous	116675082
10	89112468	89112469	G	T	16	GENIC	homozygous	116902182
10	89116937	89116938	C	T	25	GENIC	homozygous	116675096
10	89116949	89116950	A	G	29	GENIC	homozygous	116675098
10	89121809	89121810	A	G	26	GENIC	homozygous	116675102
10	89123079	89123080	C	T	18	GENIC	homozygous	116902184
10	89123146	89123147	G	A	31	GENIC	homozygous	116902186
10	89124297	89124298	G	C	19	GENIC	homozygous	116675106
10	89124581	89124582	G	C	31	GENIC	homozygous	116675108
10	89125820	89125821	T	C	21	GENIC	homozygous	116675110
10	89127412	89127413	A	G	29	GENIC	homozygous	116675112
10	89127461	89127462	A	G	22	GENIC	homozygous	116675114
10	89128621	89128622	G	T	20	GENIC	homozygous	116902188
10	89130531	89130532	G	A	30	GENIC	homozygous	116902190
10	89130550	89130551	T	C	27	GENIC	homozygous	116675118
10	89130764	89130765	T	C	23	GENIC	homozygous	116675120
10	89130808	89130809	T	A	26	GENIC	homozygous	116902192
10	89131551	89131552	A	C	23	GENIC	homozygous	116675122
10	89132622	89132623	A	G	27	GENIC	homozygous	116675124
10	89132749	89132750	A	G	18	GENIC	homozygous	116675126
10	89133423	89133424	T	C	12	GENIC	homozygous	116902194
10	89133749	89133750	G	A	24	GENIC	homozygous	116902196
10	89136494	89136495	A	C	15	GENIC	homozygous	116902198