chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	90789388	90789389	A	C	24	GENIC	heterozygous	61463620
1	90789405	90789406	T	C	27	GENIC	homozygous	61463622
1	90789737	90789738	A	G	41	GENIC	homozygous	61463628
1	90790025	90790026	A	C	31	GENIC	homozygous	61463630
1	90790061	90790062	T	G	29	GENIC	homozygous	61463632
1	90790081	90790082	A	G	24	GENIC	possibly homozygous	61463634
1	90790114	90790115	G	A	22	GENIC	homozygous	61463636
1	90790292	90790293	C	T	34	GENIC	homozygous	61463638
1	90790340	90790341	T	C	45	GENIC	homozygous	61463640
1	90790423	90790424	G	A	31	GENIC	homozygous	61463642
1	90790503	90790504	C	T	25	GENIC	homozygous	61463644
1	90790571	90790572	C	T	21	GENIC	homozygous	61463646
1	90790754	90790755	A	G	37	GENIC	homozygous	61463648
1	90790767	90790768	G	A	35	GENIC	homozygous	61463650
1	90790782	90790783	C	T	40	GENIC	homozygous	61463652
1	90790843	90790844	C	T	47	GENIC	homozygous	61463654
1	90790847	90790848	A	G	44	GENIC	homozygous	61463656
1	90790854	90790855	C	T	43	GENIC	homozygous	61463658
1	90790889	90790890	A	AC	31	GENIC	homozygous	61463660
1	90790899	90790900	T	G	31	GENIC	homozygous	61463662
1	90790969	90790970	C	T	37	GENIC	homozygous	61463664
1	90791033	90791034	A	G	34	GENIC	homozygous	61463666
1	90791572	90791573	C	T	35	GENIC	homozygous	61463668
1	90791576	90791577	T	C	34	GENIC	homozygous	61463670
1	90791720	90791721	G	A	25	GENIC	possibly homozygous	61463672
1	90791850	90791851	A	G	26	GENIC	homozygous	61463674
1	90791875	90791876	C	T	26	GENIC	homozygous	61463676
1	90792060	90792061	A	C	29	GENIC	homozygous	61463678
1	90792084	90792085	T	C	25	GENIC	homozygous	61463680
1	90792359	90792360	C	G	26	GENIC	homozygous	61463682
1	90792436	90792437	G	A	30	GENIC	homozygous	61463684
1	90789718	90789719	T	C	43	GENIC	heterozygous	61888330
1	90789852	90789853	G	C	47	GENIC	heterozygous	61888331