chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	79988464	79988466	TC		57	GENIC	homozygous	131258256
1	79988707	79988708	A	G	50	GENIC	homozygous	120898199
1	79989343	79989344	T	C	40	GENIC	homozygous	109297952
1	79989495	79989496	G	A	60	GENIC	homozygous	109297954
1	79990007	79990008	G	A	59	GENIC	homozygous	109297958
1	79990100	79990101	C	G	51	GENIC	homozygous	109297960
1	79995783	79995783		CA	36	GENIC	homozygous	131258257
1	79998402	79998403	G	A	73	GENIC	possibly homozygous	109297982
1	79990173	79990174	G	C	49	GENIC	homozygous	109297962
1	79992268	79992269	A	G	44	GENIC	homozygous	109297964
1	79994132	79994133	A	C	69	GENIC	homozygous	109297966
1	79994916	79994917	T	C	63	GENIC	homozygous	109297972
1	79995332	79995333	G	A	30	GENIC	homozygous	109297974
1	79995336	79995337	G	A	43	GENIC	homozygous	109297976
1	79995523	79995524	C	T	57	GENIC	possibly homozygous	109297978
1	79996138	79996139	T	C	58	GENIC	homozygous	109297980
1	79993311	79993312	C	T	65	GENIC	possibly homozygous	120868250
1	79998475	79998476	C	G	71	GENIC	possibly homozygous	109297984