chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	90789737	90789738	A	G	22	GENIC	possibly homozygous	61463628
1	90789829	90789830	T	C	35	GENIC	homozygous	61727273
1	90790025	90790026	A	C	26	GENIC	homozygous	61463630
1	90790061	90790062	T	G	23	GENIC	homozygous	61463632
1	90790081	90790082	A	G	25	GENIC	homozygous	61463634
1	90790114	90790115	G	A	20	GENIC	homozygous	61463636
1	90790310	90790311	A	ATT	17	GENIC	homozygous	62140938
1	90790340	90790341	T	C	14	GENIC	homozygous	61463640
1	90790423	90790424	G	A	15	GENIC	homozygous	61463642
1	90790503	90790504	C	T	17	GENIC	homozygous	61463644
1	90790582	90790583	C	T	12	GENIC	homozygous	62140939
1	90790583	90790584	T	G	11	GENIC	homozygous	62140940
1	90790754	90790755	A	G	21	GENIC	homozygous	61463648
1	90790767	90790768	G	A	19	GENIC	homozygous	61463650
1	90790782	90790783	C	T	21	GENIC	homozygous	61463652
1	90790831	90790832	C	T	26	GENIC	homozygous	62140941
1	90790843	90790844	C	T	27	GENIC	homozygous	61463654
1	90790847	90790848	A	G	27	GENIC	homozygous	61463656
1	90790854	90790855	C	T	23	GENIC	homozygous	61463658
1	90790889	90790890	A	AC	26	GENIC	homozygous	61463660
1	90790899	90790900	T	G	27	GENIC	homozygous	61463662
1	90790969	90790970	C	T	14	GENIC	homozygous	61463664
1	90790974	90790975	C	G	13	GENIC	homozygous	62140942
1	90791033	90791034	A	G	15	GENIC	homozygous	61463666
1	90791289	90791290	T	C	28	GENIC	homozygous	62140943
1	90791572	90791573	C	T	18	GENIC	homozygous	61463668
1	90791720	90791721	G	A	26	GENIC	homozygous	61463672
1	90791850	90791851	A	G	29	GENIC	homozygous	61463674
1	90791875	90791876	C	T	31	GENIC	homozygous	61463676