chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	70947667	70947668	C	G	25	GENIC	homozygous	112703812
4	70947670	70947671	C	G	26	GENIC	homozygous	112703814
4	70947686	70947687	C	T	28	GENIC	homozygous	112703816
4	70947926	70947927	T	G	38	GENIC	homozygous	112703818
4	70948019	70948020	A	G	22	GENIC	homozygous	112703820
4	70948181	70948182	A	C	31	GENIC	homozygous	112703822
4	70948523	70948524	A	G	25	GENIC	homozygous	112703824
4	70948653	70948654	A	C	24	GENIC	homozygous	112703826
4	70948664	70948665	T	G	25	GENIC	homozygous	112703828
4	70949233	70949234	C	T	25	GENIC	homozygous	112703830
4	70950397	70950398	A	G	21	GENIC	homozygous	112703832
4	70952031	70952032	A	G	34	GENIC	homozygous	112703834
4	70952366	70952367	A	G	26	GENIC	homozygous	112703836
4	70952462	70952463	T	C	23	GENIC	homozygous	112703838
4	70952983	70952984	A	G	24	GENIC	homozygous	112703840
4	70955287	70955288	A	G	27	GENIC	homozygous	112703842
4	70955654	70955655	G	T	22	GENIC	homozygous	112703844
4	70955758	70955759	T	C	20	GENIC	homozygous	112703846
4	70955880	70955881	T	C	28	GENIC	homozygous	112703848
4	70958603	70958604	C	T	15	GENIC	homozygous	112703850
4	70958995	70958995		A	28	GENIC	homozygous	128047424
4	70948670	70948671	T		21	GENIC	homozygous	128047420
4	70949603	70949603		TTCA	25	GENIC	homozygous	128047421
4	70958120	70958132	AGCTCCTACTAA		19	GENIC	homozygous	128047423
4	70962061	70962062	G	A	22	GENIC	homozygous	112703852
4	70962383	70962384	A	G	29	GENIC	homozygous	112703854
4	70962539	70962540	G	T	16	GENIC	possibly homozygous	112703856
4	70964949	70964950	C	T	26	GENIC	homozygous	112703858
4	70965429	70965430	C	A	29	GENIC	homozygous	112703860
4	70967630	70967631	C	T	20	GENIC	homozygous	112703862