chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	85130415	85130416	T	C	44	GENIC	homozygous	49020729
14	85131204	85131205	A	G	32	GENIC	homozygous	49020730
14	85131228	85131229	C	A	27	GENIC	possibly homozygous	49020731
14	85131964	85131965	T	-	28	GENIC	homozygous	49020732
14	85132488	85132490	CT	--	36	GENIC	homozygous	49020733
14	85134382	85134383	A	G	34	GENIC	homozygous	49020734
14	85135393	85135394	A	C	32	GENIC	homozygous	49020735
14	85135740	85135741	A	G	32	GENIC	homozygous	49020736
14	85135881	85135883	TG	--	12	GENIC	possibly homozygous	49020737
14	85135923	85135924	T	A	12	GENIC	heterozygous	49020738
14	85135931	85135932	A	T	11	GENIC	homozygous	49020739
14	85135950	85135951	T	G	10	GENIC	homozygous	49020740
14	85136418	85136419	C	T	31	GENIC	homozygous	49020741
14	85136925	85136926	A	AG	44	GENIC	homozygous	49020742
14	85137230	85137231	A	T	31	GENIC	homozygous	49020743
14	85137602	85137603	T	C	8	GENIC	homozygous	49020744
14	85138026	85138027	T	C	24	GENIC	homozygous	49020745
14	85138558	85138559	T	C	35	GENIC	homozygous	49020746
14	85138747	85138748	T	C	35	GENIC	heterozygous	49020747
14	85138755	85138756	C	T	29	GENIC	possibly homozygous	49020748
14	85138791	85138792	T	A	38	GENIC	homozygous	49020749
14	85138970	85138971	T	-	27	GENIC	homozygous	49020750
14	85139059	85139060	A	AG	20	GENIC	homozygous	49020751