chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	41061386	41061387	C	T	18	GENIC	homozygous	117864347
9	41061435	41061436	C	T	25	GENIC	homozygous	117716109
9	41061675	41061676	A	G	30	GENIC	homozygous	117331056
9	41061862	41061863	C	G	30	GENIC	homozygous	117716111
9	41062310	41062311	C	T	32	GENIC	homozygous	117795152
9	41062501	41062502	A	G	38	GENIC	homozygous	117864348
9	41062534	41062535	T	C	37	GENIC	homozygous	117795154
9	41062739	41062740	G	T	26	GENIC	homozygous	117805563
9	41062935	41062936	G	A	37	GENIC	homozygous	117805564
9	41063074	41063075	G	A	39	GENIC	homozygous	117716119
9	41063243	41063244	C	T	42	GENIC	homozygous	117864349
9	41063365	41063366	T	C	39	GENIC	possibly homozygous	117331057
9	41063742	41063743	T	C	31	GENIC	homozygous	117805569
9	41064058	41064059	G	A	34	GENIC	homozygous	117864350
9	41065129	41065130	T	C	30	GENIC	homozygous	117716130
9	41065297	41065298	C	T	39	GENIC	homozygous	117864351
9	41065927	41065928	C	T	7	GENIC	homozygous	117331063
9	41066419	41066420	T	G	32	GENIC	homozygous	117331064
9	41066572	41066573	C	T	24	GENIC	homozygous	117716136
9	41066605	41066606	T	C	30	GENIC	homozygous	117716138
9	41066658	41066659	G	T	31	GENIC	homozygous	117864352
9	41066669	41066670	A	T	34	GENIC	homozygous	117864353
9	41067488	41067489	G	A	7	GENIC	homozygous	117864354
9	41067686	41067687	C	T	27	GENIC	homozygous	117864355
9	41068599	41068600	G	A	24	GENIC	homozygous	117822236
9	41068666	41068667	G	A	24	GENIC	homozygous	117822237
9	41068918	41068919	A	G	34	GENIC	homozygous	117331067
9	41069344	41069345	G	A	33	GENIC	homozygous	117331068
9	41069575	41069576	C	T	25	GENIC	homozygous	117331069
9	41069833	41069834	A	G	37	GENIC	homozygous	117331070