chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13716978	13716979	A	C	25	INTERGENIC	homozygous	50062164
12	13717733	13717734	C	A	7	INTERGENIC	homozygous	50062166
12	13717748	13717749	A	AT	5	INTERGENIC	homozygous	50062168
12	13717792	13717793	G	T	4	INTERGENIC	homozygous	50364317
12	13717797	13717798	G	A	3	INTERGENIC	homozygous	50364319
12	13717800	13717801	G	A	5	INTERGENIC	heterozygous	50364321
12	13717816	13717817	C	T	6	INTERGENIC	heterozygous	50364323
12	13717817	13717818	A	G	7	INTERGENIC	heterozygous	50364325
12	13717967	13717968	T	C	13	INTERGENIC	homozygous	50062170
12	13717989	13717990	G	A	18	INTERGENIC	heterozygous	50364327
12	13717993	13717994	C	A	18	INTERGENIC	heterozygous	50364329
12	13718005	13718006	T	A	20	INTERGENIC	heterozygous	50364331
12	13718012	13718013	T	-	11	INTERGENIC	heterozygous	50062172
12	13718030	13718031	A	T	30	INTERGENIC	heterozygous	50062174
12	13718034	13718035	G	A	30	INTERGENIC	heterozygous	50062176
12	13718036	13718037	A	T	30	INTERGENIC	heterozygous	50062178
12	13718045	13718046	A	T	31	INTERGENIC	heterozygous	50062180
12	13718101	13718102	A	G	24	INTERGENIC	heterozygous	50062182
12	13718104	13718105	T	C	23	INTERGENIC	heterozygous	50364333
12	13718105	13718106	T	A	23	INTERGENIC	heterozygous	50364335
12	13718116	13718117	T	C	16	INTERGENIC	heterozygous	50062184
12	13718223	13718224	G	C	9	INTERGENIC	possibly homozygous	50281339