chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	79182085	79182086	C	T	20	GENIC	homozygous	109295977
1	79182107	79182108	C	A	18	GENIC	homozygous	108873839
1	79182387	79182388	T	C	20	GENIC	homozygous	109295979
1	79182572	79182573	C	T	33	GENIC	possibly homozygous	109295981
1	79182938	79182939	G	A	31	GENIC	homozygous	108873842
1	79183349	79183350	G	A	37	GENIC	possibly homozygous	109295983
1	79183503	79183504	T	A	22	GENIC	heterozygous	109295985
1	79183558	79183559	G	A	16	GENIC	heterozygous	109295987
1	79183622	79183623	T	C	5	GENIC	homozygous	109295988
1	79183626	79183627	T	A	5	GENIC	homozygous	109295990
1	79183689	79183690	G	A	15	GENIC	homozygous	109295992
1	79183711	79183712	A	T	16	GENIC	homozygous	109295994
1	79183775	79183776	C	T	16	GENIC	possibly homozygous	109295996
1	79184061	79184062	A	G	33	GENIC	homozygous	109295998
1	79184189	79184190	T	C	28	GENIC	homozygous	109296000
1	79184194	79184195	C	T	31	GENIC	homozygous	109296002
1	79185160	79185161	C	G	19	GENIC	homozygous	108873845
1	79185389	79185390	G	A	16	GENIC	homozygous	109296004
1	79186037	79186038	T	C	26	GENIC	homozygous	108873850
1	79186228	79186229	C	T	29	GENIC	homozygous	108873851
1	79186356	79186357	C	T	24	GENIC	homozygous	109296006
1	79186871	79186872	T	C	16	GENIC	homozygous	108873852
1	79187493	79187494	T	C	36	GENIC	homozygous	108873853
1	79187923	79187924	C	T	20	GENIC	homozygous	109296008
1	79188600	79188601	C	T	37	GENIC	homozygous	109296010
1	79188728	79188729	A	C	33	GENIC	homozygous	109296012
1	79189513	79189514	G	A	33	GENIC	homozygous	109296014