chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	45555489	45555490	C	T	14	GENIC	homozygous	126011853
4	45555618	45555619	T	G	12	GENIC	homozygous	126011855
4	45556376	45556377	A	G	15	GENIC	homozygous	126011857
4	45556769	45556770	C	T	11	GENIC	homozygous	126011859
4	45556771	45556772	T	C	8	GENIC	homozygous	126011861
4	45557489	45557490	G	T	13	GENIC	homozygous	126011863
4	45557820	45557821	T	G	23	GENIC	homozygous	126011865
4	45557976	45557977	C	G	13	GENIC	homozygous	126011867
4	45558254	45558255	A	G	8	GENIC	homozygous	126011869
4	45558264	45558265	T	C	13	GENIC	homozygous	126011871
4	45558880	45558881	G	A	13	GENIC	homozygous	126011873
4	45559765	45559766	G	A	17	GENIC	homozygous	126011877
4	45559922	45559923	C	T	22	GENIC	homozygous	126011879
4	45559966	45559967	C	A	17	GENIC	homozygous	126011881
4	45560419	45560420	A	G	20	GENIC	homozygous	126011883
4	45560452	45560453	A	G	10	GENIC	homozygous	126048522