chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5458703	5458704	C	T	34	GENIC	homozygous	109234065
20	5458771	5458772	C	T	40	GENIC	homozygous	109234066
20	5459584	5459585	A	C	37	GENIC	homozygous	109078066
20	5459813	5459814	G	A	34	GENIC	homozygous	109371230
20	5460174	5460175	C	A	31	GENIC	homozygous	109234067
20	5460458	5460459	C	T	33	GENIC	homozygous	109234068
20	5460736	5460737	A	G	38	GENIC	homozygous	109371232
20	5460968	5460969	A	C	20	GENIC	homozygous	109078072
20	5461226	5461227	T	C	36	GENIC	homozygous	109078074
20	5461370	5461371	T	G	42	GENIC	homozygous	109078076
20	5461924	5461925	T	C	32	GENIC	homozygous	109078078
20	5461965	5461966	C	G	29	GENIC	homozygous	109234070
20	5462154	5462155	G	A	8	GENIC	heterozygous	119766643
20	5462156	5462157	G	A	8	GENIC	heterozygous	119766644
20	5463944	5463945	G	A	38	GENIC	homozygous	109234071
20	5464254	5464255	T	A	15	GENIC	homozygous	109078080
20	5464341	5464342	C	T	9	GENIC	homozygous	109371234
20	5464507	5464508	T	C	26	GENIC	homozygous	109078084
20	5464810	5464811	C	T	35	GENIC	homozygous	109371236
20	5465620	5465621	G	A	38	GENIC	homozygous	109078086
20	5465983	5465984	T	C	22	GENIC	homozygous	109078090