chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	94266188	94266189	C	G	7	GENIC	homozygous	109923456
2	94266223	94266224	C	T	41	GENIC	possibly homozygous	109923458
2	94266704	94266705	C	T	25	GENIC	homozygous	109923460
2	94266816	94266817	T	C	38	GENIC	homozygous	109923462
2	94266923	94266924	A	T	35	GENIC	homozygous	109923464
2	94267068	94267069	T	C	29	GENIC	homozygous	109923466
2	94267415	94267416	C	A	28	GENIC	homozygous	109923468
2	94267911	94267912	T	C	40	GENIC	homozygous	109923470
2	94268230	94268231	A	G	33	GENIC	homozygous	109923472
2	94268500	94268501	C	T	31	GENIC	homozygous	109923474
2	94268733	94268734	T	C	31	GENIC	homozygous	109923476
2	94268887	94268888	T	C	31	GENIC	homozygous	109923478
2	94269332	94269333	C	T	40	GENIC	homozygous	109923480
2	94273287	94273288	C	T	52	GENIC	heterozygous	109923482
2	94276067	94276068	A	G	39	GENIC	homozygous	109923484
2	94276831	94276832	A	G	35	GENIC	homozygous	109923486
2	94276894	94276895	A	C	25	GENIC	homozygous	109923488
2	94277000	94277001	T	C	15	GENIC	homozygous	109923490