chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	145440759	145440760	A	T	59	GENIC	homozygous	119315523
4	145441975	145441976	C	T	51	GENIC	homozygous	119315524
4	145442116	145442117	A	G	60	GENIC	homozygous	119315525
4	145442170	145442171	A	G	56	GENIC	homozygous	112870891
4	145442882	145442883	T		55	GENIC	homozygous	132967676
4	145443014	145443015	T	A	59	GENIC	homozygous	112870892
4	145443074	145443075	A	G	43	GENIC	homozygous	119315526
4	145443138	145443139	A	G	56	GENIC	homozygous	119315527
4	145443287	145443288	A		37	GENIC	possibly homozygous	132967677
4	145443549	145443550	T	C	66	GENIC	homozygous	112870893
4	145443680	145443681	A	G	33	GENIC	homozygous	119315528
4	145443713	145443713		A	56	GENIC	homozygous	132967678
4	145443974	145443975	A	G	66	GENIC	homozygous	112870894
4	145444031	145444032	T	C	61	GENIC	homozygous	119315529
4	145444815	145444816	A	G	62	GENIC	homozygous	119315530
4	145447736	145447737	A	T	27	GENIC	possibly homozygous	132973207
4	145447738	145447739	T	A	27	GENIC	possibly homozygous	132973208
4	145447767	145447769	AA		27	GENIC	possibly homozygous	132967679
4	145447773	145447777	CACA		26	GENIC	possibly homozygous	132967680
4	145448310	145448311	C	A	65	GENIC	homozygous	112870896
4	145448855	145448856	C	A	73	GENIC	homozygous	119315531
4	145449731	145449732	A	G	59	GENIC	homozygous	119315532
4	145449876	145449877	G	A	50	GENIC	homozygous	119315533