chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	18113937	18113938	A	AC	19	GENIC	homozygous	50089631
12	18116727	18116728	A	G	39	GENIC	homozygous	50089633
12	18117453	18117454	T	C	26	GENIC	homozygous	50089635
12	18117491	18117492	G	GT	21	GENIC	homozygous	50089637
12	18117494	18117495	G	-	21	GENIC	homozygous	50089639
12	18117926	18117927	T	A	26	GENIC	homozygous	50089641
12	18118395	18118396	A	AC	32	GENIC	homozygous	50089643
12	18118883	18118884	G	A	38	GENIC	possibly homozygous	50089645
12	18119297	18119299	GG	--	24	GENIC	homozygous	50089647
12	18119892	18119893	A	AT	45	GENIC	homozygous	50089649
12	18119905	18119906	T	C	41	GENIC	possibly homozygous	50089651
12	18120180	18120181	C	CA	61	GENIC	homozygous	50089653
12	18121315	18121316	T	G	40	GENIC	heterozygous	50089655
12	18122206	18122207	C	A	40	GENIC	possibly homozygous	50089657
12	18122406	18122407	G	A	40	GENIC	possibly homozygous	50089659
12	18122901	18122902	A	G	15	GENIC	homozygous	50089661