chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	50884992	50884993	C	A	16	GENIC	homozygous	117335174
9	50885167	50885168	A	G	9	GENIC	homozygous	117335175
9	50886841	50886842	T	C	14	GENIC	homozygous	117335176
9	50890484	50890485	T	C	22	GENIC	homozygous	117335177
9	50890544	50890545	A	G	25	GENIC	homozygous	117335178
9	50890613	50890614	C	T	42	GENIC	homozygous	117335179
9	50891823	50891824	T	C	33	GENIC	homozygous	117335186
9	50893128	50893129	G	C	31	GENIC	homozygous	117335187
9	50893759	50893760	A	G	16	GENIC	homozygous	117335188
9	50894692	50894693	G	A	28	GENIC	homozygous	117335189
9	50896710	50896711	T	G	3	GENIC	homozygous	117869644
9	50896714	50896715	T	G	2	GENIC	homozygous	120353528
9	50897065	50897066	A	T	24	GENIC	homozygous	117335190
9	50898398	50898399	C	T	20	GENIC	homozygous	117335191
9	50901102	50901103	A	G	13	GENIC	homozygous	117335193
9	50902138	50902139	T	G	31	GENIC	homozygous	117335194
9	50903072	50903073	G	T	21	GENIC	homozygous	117335197
9	50903183	50903184	T	G	19	GENIC	homozygous	117335198
9	50905463	50905464	T	C	25	GENIC	homozygous	117335199
9	50912989	50912990	G	A	32	GENIC	homozygous	117335205
9	50916463	50916464	A	G	31	GENIC	homozygous	117335208
9	50917085	50917086	A	G	10	GENIC	homozygous	117335209
9	50918910	50918911	A	G	39	GENIC	homozygous	117335210