chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10966592	10966593	A	G	29	GENIC	homozygous	109091782
20	10966749	10966750	C	T	19	GENIC	homozygous	109091784
20	10966755	10966756	T	C	20	GENIC	homozygous	109091786
20	10967037	10967038	T	G	16	GENIC	homozygous	109091788
20	10967040	10967041	G	A	16	GENIC	homozygous	119768208
20	10967050	10967051	T	C	19	GENIC	homozygous	119768209
20	10967328	10967329	G	C	19	GENIC	homozygous	109091790
20	10967362	10967363	T	C	22	GENIC	homozygous	109091792
20	10967390	10967391	A	G	19	GENIC	homozygous	109091794
20	10967571	10967572	C	T	18	GENIC	homozygous	109091796
20	10967597	10967598	G	A	16	GENIC	homozygous	109091798
20	10967829	10967830	A	C	18	GENIC	homozygous	109091800