chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	41483483	41483484	A	G	28	GENIC	homozygous	109870157
19	41484012	41484013	G	A	29	GENIC	homozygous	109701774
19	41484290	41484291	C	T	20	GENIC	homozygous	109782001
19	41485043	41485044	T	G	22	GENIC	heterozygous	110170980
19	41486193	41486194	T	C	23	GENIC	homozygous	109782003
19	41486353	41486354	A	G	17	GENIC	homozygous	109782005
19	41486496	41486497	C	A	28	GENIC	homozygous	109701780
19	41486813	41486814	T	C	32	GENIC	homozygous	109701785
19	41488448	41488449	T	C	22	GENIC	homozygous	109782007
19	41489095	41489096	C	G	25	GENIC	homozygous	109701789
19	41489138	41489139	A	G	21	GENIC	homozygous	109870159
19	41489250	41489251	C	T	24	GENIC	possibly homozygous	109701793
19	41490880	41490881	T	A	29	GENIC	homozygous	109701797
19	41492691	41492692	G	A	23	GENIC	homozygous	109701799
19	41492898	41492899	A	G	24	GENIC	homozygous	109701801
19	41493397	41493398	G	C	25	GENIC	possibly homozygous	109782009
19	41493561	41493562	T	C	23	GENIC	possibly homozygous	119665565
19	41494454	41494455	C	G	21	GENIC	heterozygous	119665566
19	41496464	41496465	G	C	28	GENIC	homozygous	109701803
19	41499625	41499626	T	G	33	GENIC	homozygous	109817106
19	41500130	41500131	T	C	16	GENIC	homozygous	109701805
19	41502820	41502821	G	A	39	GENIC	homozygous	109701807
19	41503090	41503091	T	C	17	GENIC	homozygous	109701809
19	41503389	41503390	T	A	20	GENIC	homozygous	109701811
19	41503667	41503668	C	T	14	GENIC	homozygous	109701813
19	41503677	41503678	G	C	13	GENIC	homozygous	109701815
19	41505956	41505957	G	C	31	GENIC	homozygous	109701817
19	41506014	41506015	T	C	32	GENIC	homozygous	109701819
19	41506067	41506068	T	A	21	GENIC	homozygous	109701821
19	41506456	41506457	A	G	23	GENIC	homozygous	109701823
19	41507115	41507116	T	C	27	GENIC	homozygous	109701825
19	41508456	41508457	A	G	6	GENIC	homozygous	109701827