chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	19998823	19998824	T	C	63	GENIC	homozygous	111751739
16	19998863	19998866	TCC		65	GENIC	homozygous	129340186
16	19999846	19999847	T	G	79	GENIC	homozygous	111751741
16	20000254	20000255	G	A	56	GENIC	homozygous	111751743
16	20000258	20000259	C	T	57	GENIC	homozygous	111751745
16	20000352	20000353	T	G	61	GENIC	possibly homozygous	111751747
16	20003968	20003969	C	T	64	GENIC	homozygous	111751759
16	20001644	20001645	A	G	73	GENIC	homozygous	111751749
16	20001663	20001664	A	G	79	GENIC	homozygous	111751751
16	20001940	20001941	T	C	77	GENIC	homozygous	111751753
16	20002996	20002997	A	G	73	GENIC	homozygous	111751755
16	20003511	20003512	A	G	76	GENIC	homozygous	111751757
16	20004713	20004713		GTGGA	60	GENIC	homozygous	129340187
16	20005307	20005308	A	G	63	GENIC	homozygous	111751761
16	20006631	20006632	T	C	65	GENIC	possibly homozygous	111751763
16	20006689	20006690	A	C	65	GENIC	possibly homozygous	111751765
16	20006870	20006871	G	A	73	GENIC	homozygous	112292567
16	20007150	20007151	G	A	63	GENIC	homozygous	111751767
16	20007351	20007352	G	C	56	GENIC	homozygous	111751769
16	20007395	20007396	G	C	57	GENIC	homozygous	111751771
16	20009167	20009168	A	G	51	GENIC	homozygous	111751773
16	20014716	20014717	A	G	71	GENIC	homozygous	111751777
16	20006131	20006132	C	A	23	GENIC	homozygous	119099583