chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	48980204	48980205	A	AT	14	GENIC	homozygous	46258672
19	48981268	48981270	AG	--	28	GENIC	homozygous	46380835
19	48981269	48981270	G	GTTCT	28	GENIC	homozygous	46462636
19	48981773	48981774	T	C	29	GENIC	homozygous	46258674
19	48984179	48984180	G	A	42	GENIC	homozygous	46258675
19	48986325	48986326	T	A	41	GENIC	homozygous	46258676
19	48986698	48986699	A	G	31	GENIC	homozygous	46258677
19	48986960	48986961	G	C	28	GENIC	homozygous	46258680
19	48987038	48987039	G	C	30	GENIC	homozygous	46258681
19	48987116	48987117	A	G	31	GENIC	homozygous	46258682
19	48987164	48987165	G	T	37	GENIC	homozygous	46258683