chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40911382	40911383	C	A	18	GENIC	homozygous	50205004
12	40912070	40912071	T	C	27	GENIC	possibly homozygous	50205005
12	40914306	40914307	T	C	21	GENIC	possibly homozygous	50205006
12	40914573	40914574	G	T	21	GENIC	homozygous	50205007
12	40915585	40915586	G	A	21	GENIC	homozygous	50205009
12	40916202	40916203	T	TC	6	GENIC	heterozygous	50205011
12	40916203	40916204	C	-	6	GENIC	heterozygous	50323530
12	40917344	40917345	A	G	7	GENIC	heterozygous	50205012
12	40917592	40917593	T	TG	2	GENIC	homozygous	50205013