chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41833540	41833541	C	-	19	GENIC	possibly homozygous	50325878
12	41833555	41833556	G	T	16	GENIC	homozygous	50325880
12	41833573	41833574	G	-	12	GENIC	homozygous	50325882
12	41833588	41833589	G	-	13	GENIC	homozygous	50325884
12	41833637	41833638	C	A	15	GENIC	homozygous	50325886
12	41833664	41833665	C	G	16	GENIC	homozygous	50207938
12	41833673	41833674	T	A	14	GENIC	homozygous	50207939
12	41833680	41833681	T	TAA	14	GENIC	possibly homozygous	50207940
12	41833680	41833681	T	TAAA	14	GENIC	heterozygous	50207941
12	41833680	41833681	T	TA	14	GENIC	heterozygous	50382414
12	41835421	41835422	A	-	2	GENIC	homozygous	50572098