chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	48976050	48976051	G	C	29	GENIC	homozygous	114615854
13	48977303	48977304	T	C	77	GENIC	homozygous	114615856
13	48977335	48977336	T	G	68	GENIC	possibly homozygous	114615857
13	48978003	48978004	G	A	76	GENIC	possibly homozygous	114761578
13	48978286	48978287	G	T	56	GENIC	possibly homozygous	114615858
13	48978323	48978324	G	C	50	GENIC	homozygous	114615859
13	48978920	48978921	G	A	42	GENIC	homozygous	114615860
13	48979252	48979253	G	C	65	GENIC	homozygous	114761580
13	48979653	48979654	A	G	58	GENIC	homozygous	114615863
13	48980566	48980567	C	T	44	GENIC	homozygous	114615866
13	48981214	48981215	C	T	49	GENIC	homozygous	114615867
13	48982752	48982753	A	G	57	GENIC	homozygous	114615868
13	48982967	48982968	T	C	58	GENIC	homozygous	114615869
13	48983465	48983466	C	T	69	GENIC	possibly homozygous	115182236
13	48983921	48983922	T	G	42	GENIC	homozygous	114615870
13	48984011	48984012	A	C	30	GENIC	possibly homozygous	114615871
13	48984049	48984050	T	C	25	GENIC	homozygous	114615872
13	48984342	48984343	G	A	67	GENIC	homozygous	114615873
13	48984728	48984729	A	G	47	GENIC	homozygous	114857489
13	48984923	48984924	G	C	58	GENIC	homozygous	114615874
13	48985166	48985167	G	A	45	GENIC	homozygous	114761584
13	48985463	48985464	T	C	47	GENIC	homozygous	114615875
13	48985473	48985474	G	A	45	GENIC	possibly homozygous	114761586
13	48985868	48985869	T	C	58	GENIC	homozygous	114761588
13	48986905	48986906	C	T	55	GENIC	homozygous	114761590
13	48987013	48987014	A	G	61	GENIC	possibly homozygous	114615876
13	48987439	48987440	A	G	29	GENIC	homozygous	114615877
13	48987464	48987465	A	G	25	GENIC	homozygous	118497961
13	48980588	48980589	A	G	50	GENIC	possibly homozygous	118497957
13	48983797	48983798	C	T	49	GENIC	homozygous	118497958
13	48985542	48985543	G	A	38	GENIC	homozygous	118497959
13	48985744	48985745	G	A	53	GENIC	homozygous	118497960
13	48984294	48984295	A	G	62	GENIC	homozygous	114549880
13	48988206	48988207	A	C	52	GENIC	homozygous	114761594