chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	69379864	69379865	T		21	GENIC	homozygous	139843639
16	69382735	69382736	C	A	28	GENIC	homozygous	139971845
16	69385088	69385089	A	G	17	GENIC	homozygous	139971847
16	69386761	69386761		AACAG	27	GENIC	homozygous	139843641
16	69387580	69387581	C	T	30	GENIC	homozygous	139971850
16	69385832	69385834	TG		18	GENIC	homozygous	142517045
16	69384168	69384169	C	A	36	GENIC	homozygous	142571042
16	69384994	69384995	C	T	29	GENIC	homozygous	142571043
16	69386820	69386821	A	G	28	GENIC	homozygous	142571044
16	69388890	69388891	T	A	16	GENIC	homozygous	142571045
16	69389767	69389770	ATA		20	GENIC	homozygous	142517046
16	69390511	69390512	C	T	24	GENIC	homozygous	142571046
16	69392304	69392304		T	15	GENIC	possibly homozygous	139843643
16	69393107	69393108	A	G	18	GENIC	possibly homozygous	139971853
16	69394929	69394930	G	A	22	GENIC	homozygous	142571048
16	69395563	69395564	A	G	33	GENIC	homozygous	139971865
16	69395866	69395867	A	T	29	GENIC	homozygous	139971866
16	69396982	69396982		A	19	GENIC	homozygous	142517047
16	69397375	69397376	G	A	10	GENIC	homozygous	142571049
16	69398363	69398364	A	G	21	GENIC	homozygous	139971873
16	69398380	69398381	T	C	21	GENIC	homozygous	139971874
16	69398729	69398730	A	G	23	GENIC	homozygous	139971876
16	69398886	69398887	C	T	17	GENIC	homozygous	142571050
16	69398941	69398942	T	C	20	GENIC	homozygous	139971877
16	69399093	69399094	G	A	21	GENIC	homozygous	142571051
16	69399335	69399336	C	T	27	GENIC	homozygous	142571052
16	69400951	69400952	A	G	19	GENIC	homozygous	142571053
16	69401650	69401651	A	G	25	GENIC	homozygous	139971879
16	69402218	69402218		T	21	GENIC	homozygous	139843649
16	69402397	69402398	A	T	32	GENIC	homozygous	142571054