chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	49434885	49434886	A	C	26	GENIC	homozygous	116588772
10	49434939	49434940	A	T	25	GENIC	possibly homozygous	116588774
10	49435967	49435968	T	C	37	GENIC	homozygous	116588776
10	49436367	49436368	T	A	19	GENIC	homozygous	116588778
10	49436458	49436459	T	C	18	GENIC	homozygous	116588780
10	49438089	49438090	T	C	36	GENIC	homozygous	116588782
10	49438940	49438941	G	A	16	GENIC	homozygous	116588784
10	49440484	49440485	G	A	31	GENIC	homozygous	116588786
10	49440839	49440840	A	C	26	GENIC	homozygous	116588788
10	49441081	49441082	C	T	22	GENIC	homozygous	116588790
10	49441701	49441702	G	A	30	GENIC	homozygous	116588792
10	49442257	49442258	A	T	38	GENIC	homozygous	116588794
10	49443749	49443750	C	T	30	GENIC	homozygous	116588796
10	49444536	49444537	C	T	39	GENIC	homozygous	116588798
10	49444702	49444703	T	A	31	GENIC	homozygous	116588800
10	49446842	49446843	A	T	22	GENIC	homozygous	116774473
10	49446876	49446877	G	A	35	GENIC	homozygous	116588802
10	49447688	49447689	T	C	31	GENIC	homozygous	116588804
10	49448709	49448710	T	A	31	GENIC	homozygous	116588806
10	49449341	49449342	T	C	31	GENIC	homozygous	116588808
10	49450365	49450366	G	A	48	GENIC	homozygous	116588810
10	49451415	49451416	T	C	29	GENIC	homozygous	116588812
10	49453414	49453415	A	G	32	GENIC	homozygous	116588813
10	49453546	49453547	G	A	38	GENIC	homozygous	116588815
10	49453684	49453685	G	T	41	GENIC	homozygous	116588817
10	49453753	49453754	T	C	35	GENIC	homozygous	116588819
10	49453998	49453999	C	T	43	GENIC	homozygous	116588821
10	49454912	49454913	A	G	41	GENIC	homozygous	116588823
10	49455134	49455135	G	A	31	GENIC	homozygous	116588825
10	49455981	49455982	C	G	38	GENIC	homozygous	116588827
10	49457509	49457510	T	C	36	GENIC	homozygous	116588829
10	49459477	49459478	G	C	35	GENIC	homozygous	116588831
10	49460534	49460535	T	C	40	GENIC	homozygous	116774475
10	49465192	49465193	C	T	29	GENIC	homozygous	116588833