chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	24862612	24862613	G	A	10	GENIC	homozygous	47351696
16	24863113	24863114	C	CGT	6	GENIC	homozygous	47351697
16	24863203	24863204	T	A	8	GENIC	possibly homozygous	47351698
16	24863891	24863892	G	C	13	GENIC	possibly homozygous	47351699
16	24865275	24865276	A	-	15	GENIC	homozygous	47351700
16	24865298	24865299	A	G	20	GENIC	possibly homozygous	47351701
16	24865616	24865617	C	T	2	GENIC	homozygous	47351702
16	24865859	24865860	T	G	16	GENIC	possibly homozygous	47351705
16	24867070	24867071	T	-	11	GENIC	heterozygous	47351706
16	24868550	24868551	C	T	24	GENIC	possibly homozygous	47351707
16	24869407	24869408	T	A	16	GENIC	possibly homozygous	47351708
16	24869593	24869594	C	T	29	GENIC	homozygous	47351709
16	24869748	24869749	A	T	16	GENIC	possibly homozygous	47925592
16	24870612	24870613	A	G	5	GENIC	homozygous	47351710
16	24870614	24870615	T	C	5	GENIC	homozygous	47351711
16	24870647	24870648	G	A	25	GENIC	possibly homozygous	47351712
16	24870674	24870675	C	T	21	GENIC	homozygous	47351713
16	24871355	24871356	C	G	18	GENIC	homozygous	47351714