chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40911382	40911383	C	A	16	GENIC	possibly homozygous	50205004
12	40912070	40912071	T	C	15	GENIC	homozygous	50205005
12	40914306	40914307	T	C	13	GENIC	homozygous	50205006
12	40914573	40914574	G	T	12	GENIC	homozygous	50205007
12	40915585	40915586	G	A	10	GENIC	homozygous	50205009
12	40917344	40917345	A	G	10	GENIC	homozygous	50205012
12	40917592	40917593	T	TG	1	GENIC	homozygous	50205013