chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89104219	89104220	G	A	33	GENIC	homozygous	116675074
10	89105134	89105135	G	A	51	GENIC	possibly homozygous	116675076
10	89106955	89106956	C	T	52	GENIC	possibly homozygous	116950482
10	89107690	89107691	T	A	39	GENIC	homozygous	116675078
10	89107932	89107933	G	A	48	GENIC	homozygous	116675080
10	89109739	89109740	T	C	27	GENIC	homozygous	116675082
10	89113089	89113090	G	A	17	GENIC	homozygous	116675084
10	89114332	89114333	A	C	27	GENIC	possibly homozygous	116675086
10	89114560	89114561	A	G	31	GENIC	homozygous	116675088
10	89115212	89115213	T	C	46	GENIC	homozygous	116675090
10	89115501	89115502	C	T	30	GENIC	homozygous	116675092
10	89115801	89115802	A	G	34	GENIC	homozygous	116675094
10	89116937	89116938	C	T	39	GENIC	homozygous	116675096
10	89116949	89116950	A	G	38	GENIC	homozygous	116675098
10	89118814	89118815	T	G	31	GENIC	heterozygous	118007486
10	89118856	89118857	A	G	24	GENIC	homozygous	117197721
10	89119472	89119473	T	A	29	GENIC	homozygous	116950484
10	89120416	89120417	C	A	22	GENIC	homozygous	116950486
10	89125820	89125821	T	C	46	GENIC	homozygous	116675110
10	89134547	89134548	C	T	42	GENIC	heterozygous	118085568
10	89134549	89134550	C	G	41	GENIC	heterozygous	118085569
10	89134434	89134435	C	G	32	GENIC	heterozygous	118048804
10	89134511	89134512	A	T	47	GENIC	heterozygous	118048805