chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44247406	44247407	G	A	45	GENIC	possibly homozygous	115336778
12	44256099	44256100	C	A	72	GENIC	homozygous	115336780
12	44256420	44256421	C	T	48	GENIC	homozygous	115336782
12	44256511	44256512	C	T	33	GENIC	homozygous	115336784
12	44257273	44257274	G	C	41	GENIC	homozygous	115336786
12	44257305	44257306	T	G	41	GENIC	possibly homozygous	115336788
12	44257478	44257479	G	A	51	GENIC	homozygous	115336790
12	44258286	44258287	T	C	39	GENIC	homozygous	115336792
12	44258686	44258687	T	C	44	GENIC	homozygous	115336794
12	44261720	44261721	A	G	28	GENIC	homozygous	118271740
12	44261770	44261771	A	G	27	GENIC	homozygous	118271741
12	44265233	44265234	A	G	47	GENIC	homozygous	115390354
12	44265345	44265346	C	T	51	GENIC	homozygous	115336796
12	44265372	44265373	G	A	52	GENIC	homozygous	115336798
12	44267064	44267065	T	G	27	GENIC	homozygous	115390356
12	44269181	44269182	T	C	41	GENIC	homozygous	115336800
12	44269327	44269328	A	G	58	GENIC	homozygous	115336802
12	44271913	44271914	T	C	57	GENIC	homozygous	115336804
12	44276013	44276014	C	T	50	GENIC	possibly homozygous	115336806
12	44276035	44276036	C	T	49	GENIC	homozygous	115336808
12	44276542	44276543	G	A	63	GENIC	homozygous	115336810
12	44276975	44276976	G	A	31	GENIC	homozygous	115336812
12	44276978	44276979	G	A	30	GENIC	homozygous	115336814
12	44277234	44277235	A	C	41	GENIC	homozygous	115336816
12	44277873	44277874	G	A	27	GENIC	homozygous	115390368
12	44277876	44277877	G	C	27	GENIC	homozygous	115479620
12	44278964	44278965	G	C	27	GENIC	homozygous	115336820