chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	259509684	259509685	G	A	51	GENIC	homozygous	61176044
1	259509867	259509868	G	A	44	GENIC	homozygous	61329966
1	259510263	259510264	G	T	56	GENIC	homozygous	61329967
1	259510589	259510590	G	A	32	GENIC	homozygous	61329968
1	259510627	259510628	C	A	35	GENIC	homozygous	61329969
1	259510942	259510943	C	T	63	GENIC	homozygous	61329970
1	259511127	259511128	T	C	41	GENIC	homozygous	61176047
1	259511137	259511138	A	G	39	GENIC	homozygous	61329971
1	259511565	259511566	G	A	56	GENIC	homozygous	61329972
1	259511589	259511590	T	C	41	GENIC	homozygous	61329973
1	259511622	259511623	G	A	41	GENIC	homozygous	61329974
1	259511708	259511709	T	C	31	GENIC	homozygous	61329975
1	259511876	259511877	C	G	41	GENIC	homozygous	61329976
1	259512705	259512706	A	G	30	GENIC	homozygous	61329977
1	259512706	259512707	C	T	30	GENIC	homozygous	61329978
1	259513390	259513391	A	AC	39	GENIC	homozygous	61329979
1	259514005	259514006	A	T	31	GENIC	homozygous	61329980
1	259514031	259514032	T	C	32	GENIC	homozygous	61329981
1	259514379	259514380	T	TACAG	24	GENIC	homozygous	61329982
1	259514392	259514393	T	A	29	GENIC	heterozygous	61329983
1	259514544	259514545	C	G	51	GENIC	homozygous	61814869
1	259515227	259515228	A	G	18	GENIC	homozygous	61814870
1	259516321	259516324	TTG	---	22	GENIC	homozygous	61814871
1	259516718	259516719	C	T	41	GENIC	homozygous	61176053
1	259519059	259519060	C	T	41	GENIC	possibly homozygous	61814872
1	259519789	259519790	C	A	34	GENIC	homozygous	61176066
1	259520043	259520044	T	A	48	GENIC	homozygous	61329985
1	259520156	259520157	A	T	35	GENIC	possibly homozygous	61814873
1	259520378	259520379	G	A	38	GENIC	homozygous	61329986
1	259521015	259521016	C	T	43	GENIC	homozygous	61329987
1	259522027	259522028	G	T	44	GENIC	homozygous	61329988
1	259523028	259523029	A	AT	36	GENIC	homozygous	61329989
1	259523736	259523737	A	T	33	GENIC	homozygous	61176088
1	259524133	259524134	C	T	69	GENIC	homozygous	61176089
1	259524291	259524295	AAAA	----	31	GENIC	homozygous	61176090