chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	40779184	40779185	C	T	80	GENIC	homozygous	109550129
20	40783707	40783708	T	G	28	GENIC	homozygous	109550130
20	40784842	40784843	T	C	8	GENIC	homozygous	109267075
20	40785127	40785128	G	A	38	GENIC	homozygous	109315160
20	40785763	40785764	C	T	26	GENIC	homozygous	109315164
20	40785898	40785899	T	G	25	GENIC	homozygous	109315168
20	40793441	40793442	A	G	23	GENIC	homozygous	109267083
20	40793558	40793559	A	G	25	GENIC	homozygous	109267085
20	40794274	40794275	A	C	31	GENIC	homozygous	109267089
20	40794275	40794276	T	A	31	GENIC	homozygous	109267091
20	40794720	40794721	A	T	38	GENIC	homozygous	109550131
20	40795494	40795495	A	T	11	GENIC	homozygous	109315176
20	40796948	40796949	A	G	34	GENIC	homozygous	109267099
20	40797286	40797287	A	G	14	GENIC	homozygous	109267103
20	40797592	40797593	C	T	24	GENIC	homozygous	109315180
20	40799181	40799182	G	A	22	GENIC	homozygous	109550132
20	40800597	40800598	T	C	46	GENIC	homozygous	109267114
20	40800704	40800705	G	A	39	GENIC	homozygous	109267116
20	40800815	40800816	T	A	39	GENIC	homozygous	109267122