chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	50884992	50884993	C	A	11	GENIC	homozygous	117335174
9	50885167	50885168	A	G	12	GENIC	homozygous	117335175
9	50886841	50886842	T	C	24	GENIC	homozygous	117335176
9	50890484	50890485	T	C	19	GENIC	homozygous	117335177
9	50890544	50890545	A	G	23	GENIC	homozygous	117335178
9	50890613	50890614	C	T	36	GENIC	homozygous	117335179
9	50891823	50891824	T	C	26	GENIC	homozygous	117335186
9	50893128	50893129	G	C	23	GENIC	homozygous	117335187
9	50893759	50893760	A	G	13	GENIC	homozygous	117335188
9	50897065	50897066	A	T	26	GENIC	homozygous	117335190
9	50898076	50898077	T	C	24	GENIC	possibly homozygous	117869645
9	50898398	50898399	C	T	26	GENIC	homozygous	117335191
9	50901744	50901745	T	C	31	GENIC	possibly homozygous	117869646
9	50902132	50902133	C	T	43	GENIC	possibly homozygous	117869647
9	50902138	50902139	T	G	38	GENIC	homozygous	117335194
9	50903072	50903073	G	T	27	GENIC	homozygous	117335197
9	50904840	50904841	C	T	33	GENIC	possibly homozygous	117869648
9	50905463	50905464	T	C	29	GENIC	homozygous	117335199
9	50907039	50907040	A	G	29	GENIC	possibly homozygous	117869649
9	50909469	50909470	A	T	21	GENIC	homozygous	117869652
9	50912573	50912574	T	C	28	GENIC	homozygous	117335204
9	50916307	50916308	G	A	26	GENIC	homozygous	117335207
9	50916463	50916464	A	G	24	GENIC	homozygous	117335208
9	50917085	50917086	A	G	9	GENIC	homozygous	117335209
9	50917428	50917429	C	T	27	GENIC	homozygous	117869654
9	50918910	50918911	A	G	22	GENIC	homozygous	117335210
9	50920343	50920344	A	G	25	GENIC	homozygous	117869655