chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	85130415	85130416	T	C	12	GENIC	possibly homozygous	49020729
14	85131204	85131205	A	G	10	GENIC	homozygous	49020730
14	85131228	85131229	C	A	7	GENIC	heterozygous	49020731
14	85131964	85131965	T	-	6	GENIC	heterozygous	49020732
14	85132488	85132490	CT	--	8	GENIC	homozygous	49020733
14	85134382	85134383	A	G	6	GENIC	homozygous	49020734
14	85135393	85135394	A	C	8	GENIC	possibly homozygous	49020735
14	85135740	85135741	A	G	10	GENIC	homozygous	49020736
14	85135881	85135883	TG	--	6	GENIC	heterozygous	49020737
14	85135923	85135924	T	A	8	GENIC	possibly homozygous	49020738
14	85135931	85135932	A	T	3	GENIC	heterozygous	49020739
14	85136418	85136419	C	T	14	GENIC	possibly homozygous	49020741
14	85136721	85136768	TCAGGTGTCTTCCTTTATGGCTTGCCACCTCATTTTTGAGGTAGGGT	-----------------------------------------------	2	GENIC	homozygous	49431457
14	85136925	85136926	A	AG	7	GENIC	possibly homozygous	49020742
14	85137230	85137231	A	T	12	GENIC	homozygous	49020743
14	85137600	85137603	TCT	---	2	GENIC	homozygous	49452622
14	85137611	85137612	T	C	2	GENIC	homozygous	49452623
14	85138026	85138027	T	C	8	GENIC	homozygous	49020745
14	85138558	85138559	T	C	8	GENIC	heterozygous	49020746
14	85138791	85138792	T	A	5	GENIC	heterozygous	49020749
14	85138969	85138970	C	CT	1	GENIC	homozygous	49452624