chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	83645745	83645746	A	G	47	GENIC	homozygous	51520726
10	83645754	83645755	C	T	44	GENIC	homozygous	51520727
10	83645990	83645991	A	G	37	GENIC	homozygous	51520728
10	83646800	83646801	C	T	56	GENIC	homozygous	51520729
10	83647096	83647097	T	C	57	GENIC	homozygous	51520730
10	83647730	83647731	A	-	23	GENIC	possibly homozygous	51520731
10	83647868	83647875	ACCTCTC	-------	20	GENIC	homozygous	51520732
10	83647945	83647946	G	GTTTAT	37	GENIC	homozygous	51520733
10	83648401	83648405	TTTG	----	39	GENIC	homozygous	51520734
10	83648455	83648456	C	G	29	GENIC	homozygous	51520735
10	83648666	83648667	C	CTTT	3	GENIC	homozygous	51520736
10	83648761	83648762	G	A	53	GENIC	homozygous	51520737
10	83649500	83649501	A	G	55	GENIC	homozygous	51520738
10	83649846	83649847	A	G	52	GENIC	homozygous	51520739
10	83650241	83650242	C	CTTT	20	GENIC	heterozygous	51520740
10	83650241	83650242	C	CTT	20	GENIC	possibly homozygous	51520741
10	83650642	83650643	T	TG	26	GENIC	homozygous	51520742
10	83650769	83650770	T	C	47	GENIC	homozygous	51520743
10	83650923	83650924	G	A	40	GENIC	homozygous	51520744
10	83652768	83652769	G	A	50	GENIC	homozygous	51520745
10	83652892	83652893	A	-	33	GENIC	homozygous	51520746
10	83653109	83653110	C	G	42	GENIC	heterozygous	51520747