chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	50951677	50951678	G	A	13	GENIC	homozygous	56885807
4	50951702	50951703	G	T	15	GENIC	homozygous	56885809
4	50951706	50951707	C	CT	19	GENIC	homozygous	56885811
4	50951708	50951709	A	AG	19	GENIC	homozygous	56885813
4	50951717	50951718	C	G	21	GENIC	homozygous	56885816
4	50951720	50951721	T	-	21	GENIC	homozygous	56885818
4	50951725	50951726	C	-	21	GENIC	homozygous	56885820
4	50951726	50951727	C	G	21	GENIC	homozygous	58333774
4	50951730	50951731	A	G	22	GENIC	homozygous	56885822
4	50951732	50951733	T	TGTA	22	GENIC	homozygous	56885824
4	50951834	50951835	G	C	19	GENIC	possibly homozygous	56885826
4	50952042	50952043	G	C	26	GENIC	homozygous	56885828
4	50952434	50952435	T	G	25	GENIC	homozygous	56885830
4	50952571	50952572	A	T	16	GENIC	homozygous	56885832