chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	40782667	40782668	T	A	17	GENIC	homozygous	109267071
20	40784842	40784843	T	C	19	GENIC	homozygous	109267075
20	40785127	40785128	G	A	17	GENIC	homozygous	109315160
20	40785763	40785764	C	T	19	GENIC	homozygous	109315164
20	40785857	40785858	T	G	19	GENIC	homozygous	109315166
20	40785898	40785899	T	G	20	GENIC	homozygous	109315168
20	40793131	40793132	G	T	22	GENIC	homozygous	109315172
20	40793441	40793442	A	G	32	GENIC	homozygous	109267083
20	40793558	40793559	A	G	29	GENIC	homozygous	109267085
20	40794274	40794275	A	C	28	GENIC	homozygous	109267089
20	40794275	40794276	T	A	28	GENIC	homozygous	109267091
20	40794670	40794671	G	T	30	GENIC	homozygous	109315174
20	40795494	40795495	A	T	18	GENIC	homozygous	109315176
20	40796073	40796074	G	C	26	GENIC	homozygous	109315178
20	40796323	40796324	A	G	13	GENIC	homozygous	109267097
20	40796948	40796949	A	G	41	GENIC	homozygous	109267099
20	40797286	40797287	A	G	33	GENIC	homozygous	109267103
20	40797592	40797593	C	T	32	GENIC	homozygous	109315180
20	40798369	40798370	A	G	20	GENIC	homozygous	109267107
20	40800597	40800598	T	C	32	GENIC	homozygous	109267114
20	40800704	40800705	G	A	26	GENIC	homozygous	109267116
20	40800815	40800816	T	A	32	GENIC	homozygous	109267122