chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	49017515	49017516	G	C	20	GENIC	homozygous	109721725
19	49018926	49018927	G	A	29	GENIC	heterozygous	119632001
19	49019121	49019122	G	A	26	GENIC	homozygous	109721727
19	49019954	49019955	G	A	31	GENIC	homozygous	109721729
19	49020256	49020257	A	T	30	GENIC	possibly homozygous	109721730
19	49020278	49020279	A	G	26	GENIC	homozygous	109721732
19	49020717	49020718	T	G	29	GENIC	homozygous	109721734
19	49021566	49021567	G	A	19	GENIC	homozygous	109721736
19	49023511	49023512	T	C	25	GENIC	homozygous	109721738
19	49023679	49023680	G	A	31	GENIC	homozygous	109721740
19	49024273	49024274	G	A	33	GENIC	homozygous	109721742
19	49024704	49024705	G	A	35	GENIC	homozygous	109721746
19	49024828	49024829	G	A	40	GENIC	homozygous	109721748
19	49025122	49025123	A	G	17	GENIC	homozygous	109721750
19	49025311	49025312	G	A	27	GENIC	homozygous	109721752
19	49025351	49025352	G	T	24	GENIC	homozygous	109721754
19	49025458	49025459	T	G	19	GENIC	homozygous	110171364
19	49026037	49026038	A	C	20	GENIC	homozygous	109721756
19	49026081	49026082	A	G	28	GENIC	homozygous	109721758
19	49026093	49026094	A	G	27	GENIC	homozygous	109721760
19	49026790	49026791	T	C	12	GENIC	homozygous	109962877
19	49026832	49026833	T	C	6	GENIC	homozygous	119632003
19	49026838	49026839	T	C	9	GENIC	homozygous	119632004
19	49026872	49026873	C	T	19	GENIC	homozygous	119632005
19	49026934	49026935	G	A	25	GENIC	homozygous	109721762
19	49026936	49026937	C	G	25	GENIC	homozygous	109721764
19	49027102	49027103	G	A	19	GENIC	homozygous	109721766
19	49027237	49027238	T	C	20	GENIC	homozygous	109721768
19	49027527	49027528	G	A	33	GENIC	homozygous	109721770
19	49025615	49025616	C	T	11	GENIC	homozygous	109820740