chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	69186033	69186034	C	T	42	GENIC	homozygous	70800572
4	69186096	69186097	A	C	33	GENIC	homozygous	70800575
4	69186402	69186403	T	C	41	GENIC	homozygous	71538636
4	69186604	69186605	G	A	36	GENIC	homozygous	71538638
4	69186836	69186837	A	G	40	GENIC	homozygous	70800578
4	69186899	69186900	C	A	40	GENIC	possibly homozygous	70800581
4	69186905	69186906	C	T	34	GENIC	heterozygous	71538640
4	69186935	69186936	C	G	32	GENIC	heterozygous	71538642
4	69186947	69186948	G	A	29	GENIC	heterozygous	71538644
4	69186989	69186990	G	T	34	GENIC	homozygous	70800584
4	69186990	69186991	G	A	35	GENIC	homozygous	70800587
4	69187273	69187274	A	G	40	GENIC	homozygous	70800593
4	69187292	69187293	A	G	37	GENIC	homozygous	70800596
4	69187368	69187369	G	A	29	GENIC	homozygous	70800599
4	69187381	69187382	A	G	31	GENIC	homozygous	70800602
4	69187410	69187411	T	C	34	GENIC	homozygous	70800605
4	69188414	69188415	C	A	31	GENIC	homozygous	71538646
4	69188659	69188660	T	G	20	GENIC	homozygous	70800618
4	69187516	69187517	A	G	27	GENIC	homozygous	70800609
4	69187656	69187657	A	G	22	GENIC	homozygous	70800612
4	69188366	69188367	C	T	29	GENIC	homozygous	70800615
4	69188686	69188687	A	C	25	GENIC	homozygous	70800621
4	69188757	69188758	G	T	34	GENIC	homozygous	70800624