chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39415681	39415682	A	G	14	GENIC	possibly homozygous	50199117
12	39417203	39417204	C	-	3	GENIC	heterozygous	50199147
12	39417263	39417265	GG	--	9	GENIC	heterozygous	50511672
12	39417770	39417771	C	G	17	GENIC	homozygous	50199155
12	39417872	39417873	C	G	16	GENIC	homozygous	50199159
12	39418631	39418632	G	GT	1	GENIC	homozygous	50511674
12	39419011	39419012	G	GT	5	GENIC	homozygous	50511676
12	39419455	39419456	C	G	19	GENIC	possibly homozygous	50511678
12	39419849	39419850	T	A	19	GENIC	possibly homozygous	50511681
12	39420195	39420196	T	TA	3	GENIC	homozygous	50511683
12	39421208	39421209	A	G	16	GENIC	heterozygous	50199173
12	39424929	39424930	A	G	12	GENIC	homozygous	50199193
12	39425488	39425489	C	CT	13	GENIC	homozygous	50199195
12	39425495	39425496	T	C	12	GENIC	homozygous	50199197