chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	41484286	41484287	C	T	34	GENIC	homozygous	110022399
19	41484668	41484669	G	A	28	GENIC	homozygous	110022401
19	41484737	41484738	G	A	24	GENIC	homozygous	110022403
19	41486371	41486372	T	C	38	GENIC	homozygous	109701778
19	41486496	41486497	C	A	30	GENIC	homozygous	109701780
19	41486648	41486649	T	C	19	GENIC	homozygous	109701782
19	41486813	41486814	T	C	28	GENIC	homozygous	109701785
19	41488998	41488999	G	A	9	GENIC	homozygous	109701787
19	41489095	41489096	C	G	29	GENIC	homozygous	109701789
19	41489100	41489101	C	T	27	GENIC	homozygous	109701791
19	41489250	41489251	C	T	34	GENIC	homozygous	109701793
19	41489967	41489968	T	C	25	GENIC	homozygous	109701795
19	41490880	41490881	T	A	37	GENIC	homozygous	109701797
19	41492691	41492692	G	A	33	GENIC	homozygous	109701799
19	41492898	41492899	A	G	31	GENIC	homozygous	109701801
19	41496464	41496465	G	C	19	GENIC	homozygous	109701803
19	41499625	41499626	T	G	25	GENIC	homozygous	109817106
19	41500130	41500131	T	C	25	GENIC	homozygous	109701805
19	41502820	41502821	G	A	20	GENIC	homozygous	109701807
19	41503090	41503091	T	C	29	GENIC	homozygous	109701809
19	41503389	41503390	T	A	25	GENIC	homozygous	109701811
19	41503667	41503668	C	T	13	GENIC	homozygous	109701813
19	41503677	41503678	G	C	16	GENIC	homozygous	109701815
19	41505956	41505957	G	C	35	GENIC	homozygous	109701817
19	41506014	41506015	T	C	24	GENIC	homozygous	109701819
19	41506067	41506068	T	A	24	GENIC	homozygous	109701821
19	41506456	41506457	A	G	45	GENIC	homozygous	109701823
19	41508456	41508457	A	G	12	GENIC	homozygous	109701827