chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	44597505	44597506	A	G	31	GENIC	homozygous	112619388
4	44598395	44598396	T	C	43	GENIC	homozygous	112619394
4	44598416	44598417	G	A	42	GENIC	homozygous	112619396
4	44599097	44599098	C	T	43	GENIC	homozygous	112619398
4	44599431	44599432	A	T	36	GENIC	homozygous	112619400
4	44600831	44600832	T	C	46	GENIC	homozygous	112619403
4	44601346	44601347	G	A	16	GENIC	homozygous	112619405
4	44601510	44601511	C	T	15	GENIC	homozygous	112619407
4	44602168	44602169	A	G	25	GENIC	homozygous	112619409
4	44604531	44604532	G	C	35	GENIC	homozygous	112619411
4	44605720	44605721	G	A	29	GENIC	homozygous	113017962
4	44600292	44600293	A	G	41	GENIC	homozygous	113017959
4	44602601	44602602	A	G	28	GENIC	homozygous	113017960
4	44605410	44605411	C	T	29	GENIC	homozygous	113017961
4	44607298	44607299	T	C	47	GENIC	homozygous	113017963
4	44607503	44607504	G	C	54	GENIC	homozygous	113017964
4	44609052	44609053	T	C	9	GENIC	homozygous	113017965
4	44610203	44610204	C	T	33	GENIC	homozygous	113017966
4	44610929	44610930	C	T	51	GENIC	homozygous	113017967
4	44612155	44612156	G	A	47	GENIC	homozygous	113017968
4	44615000	44615001	T	A	34	GENIC	possibly homozygous	113017969
4	44615334	44615335	A	C	24	GENIC	homozygous	112619417
4	44615528	44615529	G	A	33	GENIC	homozygous	113017970
4	44616197	44616198	C	A	13	GENIC	homozygous	113017971
4	44616975	44616976	G	A	21	GENIC	homozygous	113017972
4	44618063	44618064	G	A	31	GENIC	homozygous	113017973
4	44624789	44624790	A	G	10	GENIC	homozygous	112619431
4	44625038	44625039	A	T	40	GENIC	homozygous	113017976
4	44627428	44627429	C	G	49	GENIC	homozygous	113017977
4	44628333	44628334	G	A	38	GENIC	homozygous	113017978
4	44628584	44628585	A	G	30	GENIC	homozygous	113017979
4	44628587	44628588	C	T	30	GENIC	homozygous	113017980
4	44628738	44628739	G	A	21	GENIC	homozygous	113017981
4	44629559	44629560	G	A	29	GENIC	homozygous	113017982
4	44610638	44610639	C	T	43	GENIC	homozygous	113588853