chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	49017334	49017335	T	G	29	GENIC	homozygous	109721723
19	49017515	49017516	G	C	16	GENIC	homozygous	109721725
19	49019121	49019122	G	A	53	GENIC	homozygous	109721727
19	49019954	49019955	G	A	46	GENIC	homozygous	109721729
19	49020256	49020257	A	T	42	GENIC	homozygous	109721730
19	49020278	49020279	A	G	45	GENIC	homozygous	109721732
19	49020717	49020718	T	G	49	GENIC	homozygous	109721734
19	49021566	49021567	G	A	84	GENIC	homozygous	109721736
19	49023511	49023512	T	C	44	GENIC	homozygous	109721738
19	49023679	49023680	G	A	34	GENIC	homozygous	109721740
19	49024273	49024274	G	A	35	GENIC	homozygous	109721742
19	49024410	49024411	C	A	20	GENIC	homozygous	109721744
19	49024704	49024705	G	A	25	GENIC	homozygous	109721746
19	49024828	49024829	G	A	32	GENIC	homozygous	109721748
19	49025122	49025123	A	G	37	GENIC	homozygous	109721750
19	49025311	49025312	G	A	29	GENIC	homozygous	109721752
19	49025351	49025352	G	T	35	GENIC	homozygous	109721754
19	49026037	49026038	A	C	28	GENIC	homozygous	109721756
19	49026081	49026082	A	G	28	GENIC	homozygous	109721758
19	49026093	49026094	A	G	28	GENIC	homozygous	109721760
19	49026934	49026935	G	A	27	GENIC	homozygous	109721762
19	49026936	49026937	C	G	27	GENIC	homozygous	109721764
19	49027102	49027103	G	A	47	GENIC	homozygous	109721766
19	49027237	49027238	T	C	42	GENIC	homozygous	109721768
19	49027527	49027528	G	A	37	GENIC	homozygous	109721770