chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	58202896	58202897	T	C	23	GENIC	possibly homozygous	116507588
8	58203467	58203468	G	A	24	GENIC	homozygous	118145239
8	58213779	58213780	G	T	31	GENIC	possibly homozygous	116507614
8	58214150	58214151	A	C	35	GENIC	possibly homozygous	116507616
8	58216442	58216443	C	T	23	GENIC	homozygous	116507626
8	58219010	58219011	C	T	27	GENIC	homozygous	116507630
8	58219012	58219013	C	A	25	GENIC	homozygous	116507632
8	58220601	58220602	C	T	22	GENIC	possibly homozygous	116507640
8	58221870	58221871	A	G	16	GENIC	homozygous	117910555
8	58221871	58221872	G	A	16	GENIC	homozygous	117157581
8	58222684	58222685	C	T	31	GENIC	possibly homozygous	118145241
8	58223334	58223335	T	G	12	GENIC	heterozygous	117928160
8	58225510	58225511	G	A	31	GENIC	possibly homozygous	116966301
8	58226381	58226382	G	A	28	GENIC	homozygous	116966302
8	58226457	58226458	C	T	27	GENIC	possibly homozygous	116966303
8	58228065	58228066	C	T	22	GENIC	possibly homozygous	116966304
8	58229711	58229712	A	C	24	GENIC	possibly homozygous	116507664
8	58230223	58230224	A	G	34	GENIC	possibly homozygous	116507670
8	58232865	58232866	C	T	25	GENIC	homozygous	118145243
8	58233702	58233703	A	G	29	GENIC	homozygous	118145245
8	58234741	58234742	A	C	23	GENIC	possibly homozygous	116507676
8	58234742	58234743	A	T	23	GENIC	possibly homozygous	116507678
8	58237591	58237592	T	A	13	GENIC	heterozygous	118145247
8	58237650	58237651	C	G	20	GENIC	homozygous	116507688
8	58244019	58244020	C	G	26	GENIC	possibly homozygous	116828852
8	58244321	58244322	T	C	33	GENIC	homozygous	116966308
8	58247383	58247384	T	C	34	GENIC	homozygous	116507714
8	58253984	58253985	G	A	25	GENIC	possibly homozygous	118145249
8	58255072	58255073	T	C	26	GENIC	homozygous	118145251
8	58255117	58255118	T	G	30	GENIC	homozygous	116507746