chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	67025606	67025607	G	C	2	GENIC	homozygous	46192717
19	67026525	67026526	C	CA	4	GENIC	homozygous	46192719
19	67026840	67026841	C	CCCCAACCCCCTCCAATG	1	GENIC	homozygous	46192721
19	67029017	67029018	G	A	11	GENIC	homozygous	46192725
19	67029628	67029629	A	G	7	GENIC	homozygous	46192726
19	67032870	67032871	C	T	9	GENIC	homozygous	46192728
19	67032950	67032951	C	T	8	GENIC	homozygous	46192729
19	67034000	67034001	T	C	15	GENIC	homozygous	46192730
19	67036623	67036624	T	C	8	GENIC	possibly homozygous	46192735
19	67038197	67038198	A	G	11	GENIC	homozygous	46192739
19	67038727	67038728	T	C	1	GENIC	homozygous	46192741
19	67038834	67038839	CCTGC	-----	3	GENIC	heterozygous	46192742
19	67039192	67039193	G	A	15	GENIC	possibly homozygous	46192743
19	67040198	67040199	G	GTC	1	GENIC	homozygous	46192746
19	67040861	67040862	A	T	25	GENIC	possibly homozygous	46192747
19	67040995	67040996	A	G	15	GENIC	possibly homozygous	46192748
19	67041064	67041065	G	A	10	GENIC	homozygous	46192749
19	67041167	67041168	A	G	5	GENIC	homozygous	46192750
19	67041733	67041734	G	A	11	GENIC	homozygous	46192751
19	67041763	67041764	G	T	10	GENIC	homozygous	46192752
19	67042433	67042434	C	T	23	GENIC	homozygous	46192753
19	67042812	67042813	A	T	8	GENIC	homozygous	46192754
19	67043018	67043019	C	T	8	GENIC	possibly homozygous	46192755
19	67043719	67043720	A	G	23	GENIC	possibly homozygous	46192757
19	67044601	67044602	C	T	6	GENIC	heterozygous	46192763
19	67044602	67044603	G	A	6	GENIC	heterozygous	46192764
19	67044604	67044605	A	C	6	GENIC	heterozygous	46192765