chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40911382	40911383	C	A	14	GENIC	homozygous	50205004
12	40912070	40912071	T	C	26	GENIC	homozygous	50205005
12	40913630	40913631	A	AAC	5	GENIC	heterozygous	50543799
12	40914306	40914307	T	C	19	GENIC	homozygous	50205006
12	40914573	40914574	G	T	16	GENIC	homozygous	50205007
12	40914712	40914714	TT	--	11	GENIC	heterozygous	50323524
12	40914713	40914714	T	-	11	GENIC	heterozygous	50205008
12	40915585	40915586	G	A	16	GENIC	homozygous	50205009
12	40915753	40915754	T	TTCTCCCAAG	17	GENIC	homozygous	50205010
12	40917344	40917345	A	G	10	GENIC	homozygous	50205012
12	40917592	40917593	T	TG	4	GENIC	homozygous	50205013
12	40917780	40917781	T	C	6	GENIC	homozygous	50205014