chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	87187850	87187851	A	G	18	GENIC	homozygous	51725747
10	87188050	87188051	G	A	14	GENIC	heterozygous	51725753
10	87188541	87188542	C	T	22	GENIC	homozygous	52308703
10	87188730	87188731	G	A	20	GENIC	homozygous	52308705
10	87189506	87189507	A	G	7	GENIC	homozygous	51725763
10	87189617	87189618	C	CA	2	GENIC	homozygous	51725771
10	87190959	87190960	G	A	17	GENIC	possibly homozygous	52308709
10	87192765	87192766	C	T	22	GENIC	possibly homozygous	51725785
10	87194466	87194467	G	A	8	GENIC	possibly homozygous	52308711
10	87196075	87196076	G	-	17	GENIC	homozygous	52308713
10	87197026	87197027	A	C	14	GENIC	homozygous	51922839
10	87197029	87197030	G	A	15	GENIC	possibly homozygous	51922841
10	87197195	87197196	T	G	19	GENIC	homozygous	51922843
10	87197688	87197689	T	C	12	GENIC	homozygous	51725810
10	87197972	87197973	G	A	3	GENIC	homozygous	51725813
10	87198049	87198050	G	A	7	GENIC	homozygous	51922849
10	87198290	87198291	A	G	20	GENIC	homozygous	51725815
10	87198675	87198676	C	T	19	GENIC	homozygous	52308717
10	87199172	87199173	T	A	11	GENIC	homozygous	51725821
10	87199899	87199900	G	C	15	GENIC	homozygous	51725825
10	87201903	87201904	G	A	15	GENIC	possibly homozygous	51725831
10	87202095	87202096	T	C	27	GENIC	possibly homozygous	52308719
10	87202214	87202215	G	A	6	GENIC	homozygous	52308721
10	87202229	87202230	G	A	8	GENIC	homozygous	52308723
10	87202624	87202625	C	CATTGT	3	GENIC	homozygous	51725835
10	87202628	87202629	C	CCCTGGA	3	GENIC	homozygous	51725837
10	87203193	87203194	T	C	18	GENIC	homozygous	52308725
10	87197952	87197953	A	-	1	GENIC	homozygous	52322661