chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	71464767	71464768	T	C	11	GENIC	possibly homozygous	47512638
16	71466370	71466371	T	-	22	GENIC	heterozygous	47512645
16	71466540	71466541	G	-	15	GENIC	homozygous	47512646
16	71470499	71470500	A	AGT	37	GENIC	heterozygous	47693044
16	71470504	71470506	GT	--	37	GENIC	heterozygous	47693045
16	71472252	71472253	T	-	32	GENIC	heterozygous	47693049
16	71472637	71472638	G	GA	17	GENIC	heterozygous	47512650
16	71477750	71477751	C	-	31	GENIC	homozygous	47512657
16	71477754	71477755	C	G	38	GENIC	possibly homozygous	47512658
16	71477778	71477779	T	A	36	GENIC	possibly homozygous	47512659
16	71477787	71477788	G	-	30	GENIC	homozygous	47512660
16	71477793	71477794	C	A	41	GENIC	homozygous	47512661
16	71480515	71480516	A	G	41	GENIC	homozygous	47512666
16	71480517	71480518	A	G	41	GENIC	homozygous	47512667
16	71480534	71480535	T	G	45	GENIC	homozygous	47512668
16	71480669	71480670	C	CCT	11	GENIC	homozygous	47512669
16	71480751	71480752	C	-	35	GENIC	homozygous	47512670
16	71483832	71483833	T	-	14	GENIC	heterozygous	47512674
16	71484829	71484831	TG	--	37	GENIC	heterozygous	47512676
16	71486931	71486932	T	G	46	GENIC	heterozygous	47512678
16	71489200	71489203	CCC	---	7	GENIC	heterozygous	47788797
16	71489201	71489203	CC	--	7	GENIC	heterozygous	47773052
16	71496564	71496566	TG	--	17	GENIC	heterozygous	47512684
16	71503666	71503667	T	C	32	GENIC	heterozygous	47773053
16	71513158	71513162	AGAC	----	17	GENIC	heterozygous	47693067
16	71517930	71517931	C	CT	12	GENIC	homozygous	47512728
16	71517976	71517977	C	CT	26	GENIC	homozygous	47512729
16	71518119	71518120	G	-	19	GENIC	homozygous	47512730
16	71524497	71524498	T	A	67	GENIC	heterozygous	47693072
16	71524500	71524501	G	A	54	GENIC	heterozygous	47851649
16	71529440	71529442	TT	--	32	GENIC	heterozygous	47512746
16	71529441	71529442	T	-	32	GENIC	heterozygous	47693073