chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40384896	40384897	C	CG	19	GENIC	heterozygous	50907944
12	40385213	40385214	T	TA	9	GENIC	homozygous	50203441
12	40385250	40385251	G	A	15	GENIC	homozygous	50948198
12	40385967	40385968	A	G	26	GENIC	homozygous	50948201
12	40386498	40386499	C	T	35	GENIC	homozygous	50948204
12	40386515	40386516	T	C	30	GENIC	homozygous	50948207
12	40386609	40386610	A	G	28	GENIC	homozygous	50948210
12	40387492	40387493	C	T	24	GENIC	homozygous	50948213
12	40387720	40387721	G	-	30	GENIC	possibly homozygous	50948216