chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	25714836	25714837	T	-	5	GENIC	homozygous	51365970
10	25714842	25714843	T	-	4	GENIC	homozygous	51365972
10	25716174	25716175	A	-	5	GENIC	heterozygous	51829871
10	25716660	25716661	G	T	18	GENIC	possibly homozygous	52125960
10	25723271	25723272	T	G	8	GENIC	heterozygous	52125962
10	25724856	25724857	A	C	10	GENIC	homozygous	51366048
10	25724882	25724883	T	-	2	GENIC	heterozygous	51366050
10	25724903	25724904	C	A	3	GENIC	heterozygous	51366058
10	25728322	25728323	G	A	5	GENIC	heterozygous	51366096
10	25729290	25729291	G	A	4	GENIC	heterozygous	51366112
10	25729377	25729378	C	A	1	GENIC	homozygous	52315042
10	25729378	25729379	T	A	1	GENIC	homozygous	52315043
10	25729379	25729380	C	A	1	GENIC	homozygous	52315044
10	25729385	25729386	G	C	2	GENIC	homozygous	51366114
10	25729387	25729388	A	T	2	GENIC	homozygous	51366116
10	25729403	25729404	C	A	3	GENIC	homozygous	51366118
10	25729417	25729418	C	G	3	GENIC	homozygous	51366120
10	25729432	25729433	G	T	2	GENIC	homozygous	51366124
10	25729433	25729434	C	T	2	GENIC	homozygous	51366126
10	25729440	25729441	G	A	1	GENIC	homozygous	51366128
10	25738416	25738417	G	C	12	GENIC	possibly homozygous	51366198
10	25739300	25739301	G	GA	7	GENIC	possibly homozygous	51366206
10	25740588	25740589	C	A	22	GENIC	possibly homozygous	52125964