chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40911382	40911383	C	A	39	GENIC	homozygous	50205004
12	40912070	40912071	T	C	30	GENIC	homozygous	50205005
12	40914306	40914307	T	C	47	GENIC	homozygous	50205006
12	40914573	40914574	G	T	37	GENIC	homozygous	50205007
12	40914713	40914714	T	-	3	GENIC	homozygous	50205008
12	40915585	40915586	G	A	45	GENIC	homozygous	50205009
12	40915753	40915754	T	TTCTCCCAAG	37	GENIC	homozygous	50205010
12	40916202	40916203	T	TC	3	GENIC	heterozygous	50205011
12	40917344	40917345	A	G	62	GENIC	possibly homozygous	50205012
12	40917592	40917593	T	TG	15	GENIC	homozygous	50205013
12	40917780	40917781	T	C	19	GENIC	homozygous	50205014