chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	150638213	150638214	A	G	37	GENIC	homozygous	112884481
4	150640348	150640349	G	C	44	GENIC	possibly homozygous	112884482
4	150640529	150640530	T	G	58	GENIC	homozygous	112884483
4	150640574	150640575	G	A	50	GENIC	homozygous	112884484
4	150640921	150640922	C	T	68	GENIC	possibly homozygous	112884485
4	150640946	150640947	A	G	75	GENIC	homozygous	112884486
4	150641680	150641681	C	T	52	GENIC	homozygous	112884487
4	150642805	150642806	G	A	41	GENIC	homozygous	112884488
4	150643450	150643451	A	T	52	GENIC	homozygous	112884489
4	150643841	150643842	A	C	49	GENIC	homozygous	112884490
4	150643843	150643844	A	G	49	GENIC	homozygous	112884491
4	150643882	150643883	C	T	55	GENIC	homozygous	112884492
4	150643944	150643945	C	T	43	GENIC	homozygous	112884493
4	150644026	150644027	C	T	36	GENIC	homozygous	112884494
4	150644135	150644136	G	T	42	GENIC	homozygous	112884495
4	150644429	150644430	A	G	36	GENIC	homozygous	112884496
4	150644717	150644718	C	A	40	GENIC	homozygous	112884497
4	150645090	150645091	G	A	58	GENIC	possibly homozygous	112884498
4	150645227	150645228	G	A	52	GENIC	homozygous	112884499
4	150645328	150645329	G	A	49	GENIC	homozygous	112884500
4	150645435	150645436	C	T	54	GENIC	homozygous	112884501
4	150645481	150645482	T	C	59	GENIC	homozygous	112884502