chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	24863113	24863114	C	CGT	2	GENIC	homozygous	47351697
16	24863132	24863133	T	A	5	GENIC	homozygous	47748851
16	24863203	24863204	T	A	9	GENIC	homozygous	47351698
16	24863761	24863762	G	A	18	GENIC	homozygous	47748852
16	24863891	24863892	G	C	6	GENIC	homozygous	47351699
16	24863990	24863991	G	GT	2	GENIC	heterozygous	47748853
16	24865275	24865276	A	-	21	GENIC	possibly homozygous	47351700
16	24865616	24865617	C	T	5	GENIC	homozygous	47351702
16	24866700	24866701	T	C	13	GENIC	homozygous	47748856
16	24866802	24866803	C	T	25	GENIC	homozygous	47748857
16	24867027	24867028	C	CT	17	GENIC	possibly homozygous	47748858
16	24867757	24867758	A	G	25	GENIC	possibly homozygous	47748859
16	24868550	24868551	C	T	19	GENIC	possibly homozygous	47351707
16	24869187	24869188	C	T	14	GENIC	possibly homozygous	47748860
16	24869201	24869202	G	A	11	GENIC	homozygous	47748861
16	24869407	24869408	T	A	18	GENIC	heterozygous	47351708
16	24869649	24869653	TAAG	----	9	GENIC	homozygous	47748862
16	24869717	24869718	G	C	16	GENIC	homozygous	47748863
16	24869748	24869749	A	-	13	GENIC	homozygous	47748864
16	24870274	24870275	C	G	20	GENIC	possibly homozygous	47748865
16	24871355	24871356	C	G	8	GENIC	homozygous	47351714
16	24871699	24871700	C	T	4	GENIC	homozygous	47748869
16	24871737	24871738	C	A	6	GENIC	homozygous	47748870