chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	84000887	84000888	G	T	23	GENIC	homozygous	108879826
1	84000888	84000889	A	T	22	GENIC	homozygous	108879827
1	84001089	84001090	G	C	25	GENIC	homozygous	108879828
1	84001210	84001211	C	T	28	GENIC	homozygous	108879829
1	84001389	84001390	A	C	20	GENIC	homozygous	108879830
1	84001618	84001619	G	A	28	GENIC	homozygous	108879831
1	84002273	84002274	G	T	27	GENIC	homozygous	108879832
1	84002472	84002473	C	T	23	GENIC	homozygous	108879833
1	84002830	84002831	T	C	25	GENIC	homozygous	108879834
1	84002840	84002841	G	T	24	GENIC	possibly homozygous	108879835
1	84003270	84003271	T	C	31	GENIC	homozygous	108879836
1	84003539	84003540	T	C	15	GENIC	homozygous	108879837
1	84003614	84003615	A	G	27	GENIC	homozygous	108879838
1	84003787	84003788	T	C	17	GENIC	homozygous	108879839
1	84004000	84004001	C	T	27	GENIC	homozygous	108879840
1	84004758	84004759	A	C	36	GENIC	homozygous	108879841
1	84005270	84005271	T	C	22	GENIC	homozygous	108879842
1	84005782	84005783	C	G	26	GENIC	homozygous	108879843
1	84007671	84007672	C	T	21	GENIC	homozygous	108879844
1	84008145	84008146	A	T	17	GENIC	homozygous	108879845
1	84008410	84008411	C	A	24	GENIC	homozygous	108879846