chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13715986	13715987	G	C	31	INTERGENIC	homozygous	50281326
12	13716134	13716135	A	G	27	INTERGENIC	homozygous	50281327
12	13716766	13716767	A	G	11	INTERGENIC	homozygous	50281328
12	13716769	13716770	G	A	12	INTERGENIC	homozygous	50281329
12	13716963	13716964	G	T	29	INTERGENIC	homozygous	50281330
12	13716977	13716978	A	C	28	INTERGENIC	homozygous	50281331
12	13717507	13717518	GACAACCAACA	-----------	16	INTERGENIC	homozygous	50281332
12	13717522	13717523	G	A	13	INTERGENIC	homozygous	50281333
12	13717576	13717577	G	A	21	INTERGENIC	homozygous	50281334
12	13717616	13717617	C	T	20	INTERGENIC	homozygous	50281335
12	13716978	13716979	A	C	28	INTERGENIC	homozygous	50062164
12	13717748	13717749	A	AT	7	INTERGENIC	homozygous	50062168
12	13718141	13718224	GTAGGCAAATGGTTGGAACTGGAAAATGTCATCTGAGTGAGGTAACCCAATCACAGAAAAACAGACATGGTATGCACTCATTG	-----------------------------------------------------------------------------------	12	INTERGENIC	heterozygous	50503875
12	13718684	13718685	C	T	22	INTERGENIC	homozygous	50281340
12	13718225	13718226	T	TAAGTGGCTATTA	9	INTERGENIC	heterozygous	50556943