chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	90370030	90370031	C	T	21	GENIC	homozygous	61462127
1	90370711	90370712	C	T	18	GENIC	homozygous	61462129
1	90370717	90370718	G	A	17	GENIC	homozygous	61462131
1	90370845	90370846	G	T	25	GENIC	homozygous	61462133
1	90371370	90371371	A	G	16	GENIC	homozygous	61462135
1	90371932	90371933	A	C	9	GENIC	homozygous	61462137
1	90372061	90372062	G	C	11	GENIC	possibly homozygous	61462139
1	90373436	90373437	C	T	17	GENIC	homozygous	61462141
1	90375948	90375949	C	A	25	GENIC	homozygous	61462142
1	90376553	90376554	A	G	17	GENIC	homozygous	61462143
1	90377689	90377690	A	G	22	GENIC	homozygous	61462145
1	90377744	90377745	A	G	20	GENIC	homozygous	61462146
1	90377813	90377814	A	G	18	GENIC	homozygous	61462148
1	90378009	90378011	AC	--	2	GENIC	homozygous	60759053
1	90378112	90378113	T	TA	12	GENIC	homozygous	61462150
1	90378612	90378613	T	A	21	GENIC	homozygous	61462152
1	90378719	90378720	G	A	15	GENIC	heterozygous	61462154
1	90378729	90378730	C	T	15	GENIC	possibly homozygous	61462156
1	90378760	90378761	T	C	13	GENIC	possibly homozygous	61462158
1	90380686	90380687	G	A	11	GENIC	homozygous	61462160
1	90380858	90380859	T	C	9	GENIC	homozygous	61462162